U.S. patent application number 13/711221 was filed with the patent office on 2013-04-25 for system and method for managing a patient.
This patent application is currently assigned to GUARDSMAN SCIENTIFIC, INC.. The applicant listed for this patent is Guardsman Scientific, Inc.. Invention is credited to Daniel Vezina.
Application Number | 20130102899 13/711221 |
Document ID | / |
Family ID | 41066575 |
Filed Date | 2013-04-25 |
United States Patent
Application |
20130102899 |
Kind Code |
A1 |
Vezina; Daniel |
April 25, 2013 |
SYSTEM AND METHOD FOR MANAGING A PATIENT
Abstract
A system for managing a patient is disclosed and can include a
patient interface adapted to obtain ultrasound information about
the patient, a provider interface adapted to facilitate
communication between the system and a provider, and a controller
in communication with the patient interface and the provider
interface, the controller including a clinical management module
adapted to receive the ultrasound information and to recommend a
clinical management strategy based upon the ultrasound information.
A method of presenting a clinical management strategy is also
described including obtaining information regarding a condition of
a patient, developing a determinant reflecting the condition, and
presenting a user with a clinical management strategy on an output
device.
Inventors: |
Vezina; Daniel; (Park City,
UT) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Guardsman Scientific, Inc.; |
Park City |
UT |
US |
|
|
Assignee: |
GUARDSMAN SCIENTIFIC, INC.
Park City
UT
|
Family ID: |
41066575 |
Appl. No.: |
13/711221 |
Filed: |
December 11, 2012 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12536247 |
Aug 5, 2009 |
8348847 |
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13711221 |
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61224621 |
Jul 10, 2009 |
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61140767 |
Dec 24, 2008 |
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61086254 |
Aug 5, 2008 |
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Current U.S.
Class: |
600/438 ;
600/450 |
Current CPC
Class: |
A61B 8/13 20130101; A61B
8/06 20130101; A61B 8/4472 20130101; A61B 5/02028 20130101; A61B
8/52 20130101; A61B 8/4477 20130101; A61B 8/565 20130101; A61B 8/04
20130101; A61B 8/065 20130101; G16H 40/67 20180101; A61B 8/00
20130101; G16H 20/40 20180101; A61B 8/0883 20130101; A61B 8/5292
20130101; G16H 30/20 20180101; A61B 8/54 20130101 |
Class at
Publication: |
600/438 ;
600/450 |
International
Class: |
A61B 8/08 20060101
A61B008/08; A61B 8/06 20060101 A61B008/06; A61B 8/04 20060101
A61B008/04; A61B 8/13 20060101 A61B008/13; A61B 8/00 20060101
A61B008/00 |
Claims
1. A system for hemodynamically managing a patient, the system
comprising: a) a patient interface configured to capture first
cardiac image data regarding the patient; b) a database comprising
second cardiac image data stored in the database; and c) a
controller in communication with the database and patient
interface, the controller configured to compare the first cardiac
image data to the second cardiac image data, the controller
categorizing the first cardiac image data according to a category
of the second cardiac image data the first cardiac image data most
closely resembles.
2. The system of claim 1, wherein the controller identifies an
intervening hemodynamic treatment measure correlated with the
category of the second cardiac image data the first cardiac image
data most closely resembles.
3. The system of claim 2, further comprising a provider interface
configured to display the intervening hemodynamic treatment
measure.
4. The system of claim 2, wherein the intervening hemodynamic
treatment measure is correlated in the database with the category
of the second cardiac image data the first cardiac image data most
closely resembles.
5. The system of claim 2, wherein the intervening hemodynamic
treatment measure comprises at least one of the following: reducing
afterload; maintaining afterload; reducing preload; maintaining
preload; increasing preload; or inotropic support.
6. The system of claim 1, wherein the category of the second
cardiac image data is associated with at least one of the following
hemodynamic conditions: low cardiac output; normal cardiac output;
low left ventricular filling pressure; normal left ventricular
filling pressure; or high left ventricular filling pressure.
7. The system of claim 1, wherein the category of the second
cardiac image data is associated with at least one of the following
hemodynamic conditions: contractile function, valvular function;
left ventricular diastolic function; left ventricular filling
pressure; pulmonary artery pressure; or cardiac output.
8. The system of claim 1, wherein the patient interface comprises
an ultrasound probe and the first cardiac image data comprises a
cardiac ultrasound image.
9. The system of claim 8, wherein the second cardiac image data
comprises a cardiac ultrasound image.
10. The system of claim 1, wherein the second cardiac image data
comprises a cardiac ultrasound image.
11. The system of claim 1, further comprising image recognition
software used to analyze the first cardiac image data.
12. The system of claim 1, wherein the second cardiac image data
comprises video images.
13. The system of claim 12, wherein the video images comprise a
video loop.
14. The system of claim 1, wherein the second cardiac image data
comprises a still video image.
15. The system of claim 1, wherein the patient interface comprises
multiple ultrasound probes configured to be attached to the patient
at different spaced-apart cardiac ultrasound windows of the
patient.
16. A method for hemodynamically managing a patient, the method
comprising: a) capturing via a patient interface first cardiac
image data regarding the patient; b) accessing second cardiac image
data that is stored in a database; c) comparing via a controller in
communication with the database the first cardiac image data to the
second cardiac image data; and d) categorizing via the controller
the first cardiac image data according to a category of the second
cardiac image data the first cardiac image data most closely
resembles.
17. The method of claim 16, further comprising identifying via the
controller an intervening hemodynamic treatment measure correlated
with the category of the second cardiac image data the first
cardiac image data most closely resembles.
18. The method of claim 17, further comprising displaying on a
provider interface the intervening hemodynamic treatment
measure.
19. The method of claim 17, wherein the intervening hemodynamic
treatment measure is correlated in the database with the category
of the second cardiac image data the first cardiac image data most
closely resembles.
20. The method of claim 17, wherein the intervening hemodynamic
treatment measure comprises at least one of the following: reducing
afterload; maintaining afterload; reducing preload; maintaining
preload; increasing preload; or inotropic support.
21. The method of claim 16, wherein the category of the second
cardiac image data is associated with at least one of the following
hemodynamic conditions: low cardiac output; normal cardiac output;
high cardiac output; low left ventricular filling pressure; normal
left ventricular filling pressure; or high left ventricular filling
pressure.
22. The method of claim 16, wherein the category of the second
cardiac image data is associated with at least one of the following
hemodynamic conditions: contractile function; valvular function;
left ventricular diastolic function; left ventricular filling
pressure; pulmonary artery pressure; or cardiac output.
23. The method of claim 16, wherein the patient interface comprises
an ultrasound probe and the first cardiac image data comprises a
cardiac ultrasound image.
24. The method of claim 23, wherein the second cardiac image data
comprises a cardiac ultrasound image.
25. The method of claim 16, wherein the second cardiac image data
comprises a cardiac ultrasound image.
26. The method of claim 16, wherein the comparison of step c)
comprises using image recognition software to analyze the first
cardiac image data.
27. The method of claim 16, wherein the second cardiac image data
comprises video images.
28. The method of claim 27, wherein the video images comprise a
video loop.
29. The method of claim 16, wherein the second cardiac image data
comprises a still video image.
30. The method of claim 1, wherein the patient interface comprises
first and second ultrasound probes and wherein the method further
comprises attaching the first ultrasound probe to the patient at a
first cardiac ultrasound window of the patient and attaching the
second cardiac ultrasound probe to the patient at a second cardiac
ultrasound window, the first and second cardiac ultrasound windows
being spaced-apart from each other, and the first and second
ultrasound probes being attached to the patient over a common time
period.
31. The method of claim 30, wherein the first cardiac ultrasound
window comprises one of a transthoracic parasternal window, a
transthoracic apical window, a sub-costal window, or a suprasternal
notch window, and the second cardiac ultrasound window comprises
one of the transthoracic parasternal window, the transthoracic
apical window, the sub-costal window, or the suprasternal notch
window that is not the first cardiac ultrasound window.
Description
CROSS REFERENCE TO RELATED CASES
[0001] This application is a continuation application of U.S.
application Ser. No. 12/536,247 filed Aug. 5, 2009, which
application claims priority to U.S. Provisional Application
61/086,254, which was filed on Aug. 5, 2008, and U.S. Provisional
Application 61/224,621, which was filed on Jul. 10, 2009, each
entitled System (apparatus and method) to guide clinical
hemodynamic management of patients requiring anesthetic care,
perioperative care and critical care using cardiac ultrasound. The
present application also claims priority to U.S. Provisional
Application 61/140,767, which was filed on Dec. 24, 2008 and
entitled Peripheral Ultrasound System (apparatus and method) for
automated and uninterrupted data acquisition. The disclosures of
each of the aforementioned applications are hereby incorporated by
reference herein in their entireties.
FIELD OF THE INVENTION
[0002] The present disclosure relates to patient management. More
particularly, the present disclosure relates to monitoring,
responding to, and reporting on patient conditions. Even more
particularly, the patient conditions can relate to circulatory
function or hemodynamic status.
BACKGROUND
[0003] Proper circulatory function is essential to sustain and
prolong life. From a more practical standpoint, circulatory
function can be a factor affecting health care costs resulting from
complications, hospital readmissions, and mortality. According to
some professionals, ensuring the adequacy of circulatory function
is one of the most important clinical goals of healthcare providers
for anesthetic, perioperative, or critical care procedures.
Currently, the American Society of Anesthesiology (ASA) endorses
the use of the EKG monitor, systemic blood pressure (BP), pulse
oximeter, and urine output (UO), known as the conventional
parameters, as the basic standard of care for assessing circulatory
function. However, these conventional parameters may not always
provide suitable information for managing circulatory function.
[0004] Using conventional parameters may be clinically acceptable
for patients with normal cardiovascular function. However,
conventional parameters often provide incomplete information for
patients with cardiovascular risk factors and/or comorbidities. For
example, in surgical and critical care settings, managing the
circulatory function of a congestive heart failure (CHF) patient
with conventional parameters can lead a practitioner to deliver
inappropriate amounts of intravenous (IV) fluid and/or maintain an
inappropriate level of blood pressure leading to volume overload of
the circulatory system of the patient. As a result of the
incomplete information, many patients currently undergoing surgical
procedures and/or requiring critical care medicine may not receive
optimal hemodynamic management. This can lead to cardiovascular
complications, hospital readmission, and/or mortality. This result
is both detrimental to the health of the patient and costly to the
health care system.
[0005] This weakness in the standard of care is exacerbated by the
fact that CHF, with normal or reduced contractile function, is the
leading admission diagnosis for medicine and cardiology services in
the United States. Further adding to the problem is that diastolic
dysfunction, often the underlying cause of CHF, is common among the
baby boomer population. For individuals over 65, 53.8% suffer from
some degree of diastolic dysfunction. (40.7% mild and 13.1%
moderate or severe). The number of individuals over 65 has been
projected to increase by 50% from 2000 to 2020 and as a result, the
baby boomer population is recognized as a driving force for
healthcare services.
[0006] Conventional circulatory function parameters may provide
incomplete information for patients with cardiovascular risk
factors and/or comorbidities. CHF is an example of one of those
conditions and is also a common condition among the baby boomer
population and the population as a whole. The health related and
economic costs associated with complications, readmissions, and
mortality rates need to be addressed. Accordingly, there is a need
for a more capable system for managing the hemodynamics of
patients.
SUMMARY
[0007] In one embodiment, a system for assisting a provider in
managing a patient may include a patient interface adapted to
obtain ultrasound information about the patient. The system may
also include a provider interface adapted to facilitate
communication between the system and the provider. The system may
include a controller in communication with the patient interface
and the provider interface, the controller including a clinical
management module adapted to receive the ultrasound information and
to recommend a clinical management strategy based upon the
ultrasound information.
[0008] In another embodiment, a method of presenting a clinical
management strategy for a patient may include obtaining ultrasound
information regarding a condition of the patient from an ultrasound
probe, communicating the ultrasound information to a controller in
communication with the ultrasound probe, employing the controller
to develop from the ultrasound information a determinant reflecting
the condition of the patient, and providing on an output device in
communication with the controller a clinical management strategy
based on the determinant.
[0009] In another embodiment, a method of developing a
cardiovascular determinant of a patient, may include receiving
ultrasound information from a patient interface, the patient
interface being adapted to obtain ultrasound information related to
cardiovascular function status of the patient, processing the
ultrasound information to determine the cardiovascular function
status of the patient, and sending the status to a clinical
management module for the development of a clinical strategy.
[0010] In another embodiment, a method of suggesting a clinical
management strategy may include comparing a first order data point
to a plurality of categories, where the first order data point is
associated with ultrasound information, assigning a category from
the plurality of categories to the first order data point based on
which category of the plurality of categories, the first order data
point falls, selecting a recommended intervening measure based on
the assigned category, and presenting the recommended intervening
measure on a display.
[0011] In another embodiment, a method of managing a patient may
include positioning ultrasound probes on a patient, the ultrasound
probes being in communication with a controller, using an input
device to instruct the controller to obtain cardiovascular function
information from the patient via the ultrasound probes, reviewing a
suggested clinical management strategy, the strategy including a
recommended intervening measure and being based on the
cardiovascular function information, deciding whether to conduct
the recommended intervening measure, a different intervening
measure, or no intervening measure.
[0012] In another embodiment, a method of monitoring a patient may
include monitoring a patient via ultrasound and generating
information from the ultrasound. The method may also include, based
upon the information, recording a clinical finding and recommending
and recording an intervening measure, displaying a list of clinical
findings including the clinical finding and related clinical
findings, prompting a user to select from the list of clinical
findings, displaying a list of intervening measures including the
intervening measure and related intervening measures, prompting the
user to select from the list of intervening measures, compiling a
report including the selected clinical finding and the selected
intervening measure.
BRIEF DESCRIPTION OF THE FIGURES
[0013] FIG. 1 shows a system for managing a patient according to
certain embodiments.
[0014] FIG. 2 is a schematic cross-sectional view of a probe
according to certain embodiments.
[0015] FIG. 3 is a schematic view of an external imaging plane
mechanism.
[0016] FIG. 4 is a schematic view of an internal imaging plane
mechanism.
[0017] FIG. 5 is a side view of a probe according to certain
embodiments.
[0018] FIG. 6 is a top view of a probe positioned on a patient
according to certain embodiments.
[0019] FIG. 7 is a front view of a connecting pad according to
certain embodiments.
[0020] FIG. 8 is an isometric view of one embodiment of a
connecting pad.
[0021] FIGS. 9 & 10 are each front views of a display according
to certain embodiments.
[0022] FIG. 11 is a schematic view of a controller according to
certain embodiments.
[0023] FIG. 12 is an exemplary 2D black and white ultrasound image
display according to certain embodiments.
[0024] FIG. 13 is an exemplary color Doppler image display
according to certain embodiments.
[0025] FIG. 14 is and exemplary spectral Doppler image display
according to certain embodiment.
[0026] FIG. 15 is a chart showing categories for statuses of
several cardiovascular determinants according to certain
embodiments.
[0027] FIGS. 16-27 are each charts reflecting clinical management
strategy processes according to one or more embodiments.
[0028] FIG. 28 is an exemplary report input screen for use in
preparing a report.
[0029] FIG. 29 is an exemplary report.
[0030] FIG. 30 is an exemplary list of an international
classification of diseases for use in preparing a DRG report.
[0031] FIG. 31 is an exemplary DRG report.
[0032] FIG. 32 is an exemplary professional billing report.
[0033] FIGS. 33-36 are each charts reflecting steps taken to obtain
patient information according to certain embodiments.
[0034] FIG. 37 is a chart showing steps taken by a hemodynamic
management system to assist in managing a patient according to
certain embodiments.
[0035] FIG. 38 is a chart showing a method of presenting a clinical
management strategy for a patient.
[0036] FIG. 39 is a chart showing a method of developing a
cardiovascular determinant of a patient.
[0037] FIG. 40 is a chart showing a method of suggesting a clinical
management strategy.
[0038] FIG. 41 is a chart showing a method of managing a
patient.
[0039] FIG. 42 is a chart showing a method of monitoring a
patient.
DETAILED DESCRIPTION
[0040] The present disclosure relates to a hemodynamic management
system. The system can be an ultrasound based system capable of
non-invasive monitoring of circulatory function including cardiac
output and filling pressures. The system can be used for live
monitoring of patients in a clinical setting. The system can also
be used for patients undergoing anesthetic, perioperative, critical
care, or other procedures and can assist in developing clinical
management strategies. The live monitoring may allow providers in
this setting to obtain circulatory function information previously
limited to a diagnostic ultrasound setting. Access to this
information in these procedural settings may allow providers to
actively manage patients' circulatory function during a procedure.
Moreover, the hemodynamic management may be more suitable than that
which was available with the conventional parameters described
above.
[0041] Referring now to FIG. 1, a system is shown including a
patient interface 100, a controller 102, a provider interface 104,
an auxiliary device interface 106, and a network interface 108. The
system can preferably be a hemodynamic management system where the
patient interface 100 includes one or more probes 110, the
controller 102 is a hemodynamic controller, and the provider
interface 104 is an input and/or output device or system. The
hemodynamic management system can allow the controller 102 to
access circulatory information relating to a patient through the
patient interface 100 and the provider interface 104 can be used to
facilitate the activities of the controller 102 and to receive
output information from the controller 102. In a preferred
embodiment, the auxiliary device interface 106 may function to
interface with devices related to conventional parameters such as
an EKG or a blood pressure monitor, but other devices may also be
connected through the auxiliary device interface 106. The network
interface 108 can function, preferably, for use in remote
supervision or quality assessment, but may be adapted for other
types of network communication and data transmission.
[0042] The patient interface 100 can include one or more probes 110
adapted to be positioned on a patient and adapted to obtain
information about a patient. Preferably, the probes 110 can be
adapted to obtain circulatory function information about a patient.
The probes 110 can be in the form of a transducer adapted to
alternate between sending and receiving signals. For example, in a
preferred embodiment the probes 110 can be ultrasonic transducers
adapted to intermittently or continuously produce and detect
ultrasonic waves.
[0043] The probes 110 can be positioned on a patient in a suitable
location related to the information desired to be collected by any
given probe 110. In a preferred embodiment, the probes 110 can be
adapted to gather information relating to the hemodynamic status of
a patient. In this embodiment, the probes 110 can be positioned in
suitable locations for gathering information about the heart and
may be referred to herein as cardiac probes 110. Accordingly, the
probes 110 can be placed in one of several available windows. A
window can be defined as a transducer location from where the heart
can be imaged using ultrasound-based imaging and the windows can be
external or internal to the patient's body. In a preferred
embodiment, four external cardiac probes 110A-D can be provided and
can be positioned in the transthoracic parasternal window, the
transthoracic apical window, the sub-costal window, and the
suprasternal notch window, respectively.
[0044] The transthoracic parasternal window can be defined as being
located on the left side of the sternum between the 3.sup.rd and
4.sup.th rib. The transthoracic apical window can be defined as
being located on the chest between the 5.sup.th and 6.sup.th left
ribs posterior and lateral to the nipple line. The sub-costal
window can be defined as being located under the right costal ridge
and directed toward the left shoulder. The suprasternal notch
window can be defined as being located at the suprasternal
notch.
[0045] Preferably, an internal cardiac probe 110E can also be
provided in the mid-esophageal window and thus can be positioned
midway down the esophagus. In the preferred embodiment, a sixth
probe 110F can be included in the form of an external non-cardiac
probe 110. The sixth probe 110F can be adapted to image superficial
non-cardiac structures outside the chest.
[0046] Additional or fewer probes 110 can be provided. The probes
110 can all be of the same type or they may differ and combinations
of probe type or style can be included. Preferably the probes 110
can all be ultrasonic transducers. Alternatively, some of the
probes 110 may include pressure, electrical signal, or temperature
sensors in lieu of ultrasonic transducers and other probe types can
be provided.
[0047] Referring to FIG. 2, in a preferred embodiment, the four
external cardiac probes 110A-D are ultrasonic transducers. The
probes 110A-D can have a relatively low profile with a height 111
of between approximately 1 cm to approximately 10 cm. Preferably,
the height 111 is between approximately 2 cm to approximately 8 cm.
The probes 110A-D can have a surface contact area of approximately
1 cm to 3 cm by approximately 3 cm to 8 cm, or approximately 3 to
24 cm.sup.2. Preferably, the contact area is approximately 2 cm by
approximately 5 cm, or approximately 10 cm.sup.2.
[0048] In a preferred embodiment, the internal cardiac probe 110E
is also an ultrasonic transducer. The probe 110E can be
approximately 1 cm to 2 cm by approximately 2.5 cm to 3.5 cm, or
approximately 2.5 to 7 cm.sup.2. Preferably, the internal cardiac
probe 110E is approximately 1.5 cm by 3 cm, or approximately 4.5
cm.sup.2.
[0049] In a preferred embodiment, the external non-cardiac probe
110F can also be an ultrasonic transducer with a higher frequency
than the cardiac probes 110A-E and thus adapted for imaging more
superficial structures. For example, the external non-cardiac probe
110F may be used to identify superficial vascular structures
outside the chest. As used herein, superficial can be understood to
mean less than approximately 12 cm under the skin or preferably
less than 10 cm under the skin. The probe 110F can be used when
inserting a central line or a peripheral venous or arterial
catheter. Alternatively or additionally, the probe 110F can be used
for identifying large nerve bundles of the neck or an upper or
lower extremity when performing a peripheral nerve blockade for
surgical or post-operative pain control. The external non-cardiac
probe 110F can have a height of between approximately 1 cm to
approximately 12 cm. Preferably, the height is between
approximately 2 cm and 8 cm. The external non-cardiac probe 110F
can have a surface contact area of approximately 1 to 3 cm by
approximately 8 to 10 cm, or approximately 8 to 30 cm.sup.2.
Preferably, the external non-cardiac probe 110F has a contact area
of 2 cm by 8 to 10 cm, or 16 to 20 cm.sup.2.
[0050] In a preferred embodiment, each of the external or internal
probes 110 can be adapted for obtaining information suitable for
two-dimensional imaging, three-dimensional imaging, B-mode, M-mode,
color Doppler, and spectral Doppler output. The probes 110 can be
built with piezo-electric crystals 113 adapted to emit ultrasonic
signals. The probes 110 can include a suitable crystal array. For
example, the cardiac probes 110 can be constructed with a phased
array of crystals or a matrix of a phased array of crystals. The
phased array of crystals may provide for a two dimensional
pie-shaped cross-sectional image. The matrix may provide for a
three dimensional image. The probes 110 adapted to image more
superficial elements can be constructed with a linear array of
crystals allowing for higher frequency imaging and may provide for
a rectangular image. Other arrangements of crystals such as, for
example, a circular array can be used and are within the scope of
the disclosure. Moreover, mechanical transducers could be used in
lieu of or in addition to the piezo-electric crystal type
transducers described. In other embodiments the probes 110 can be
adapted to obtain other information such as temperature, pressure,
moisture, EKG signals, electrical signals, or other information
indicative of patient condition. Accordingly, the probes 110 can
take the form of a thermometer or a pressure transducer or sensor.
The probes 110 can monitor other conditions and can take the form
of other suitable devices adapted to detect and/or measure a
condition.
[0051] Referring generally to FIGS. 3 and 4, the probes 110 can
include a variable probe view. In a preferred embodiment, the probe
view can be adjusted with an imaging plane mechanism 112 allowing
each probe 110 of the system to acquire optimal quality images with
minimal or no intervention by the provider. The mechanism 112 can
be adapted to allow for adjustment of the imaging plane of the
probe 110 by providing a rotation angle adjustment and an elevation
angle adjustment. In some embodiments, this mechanism 112 may be
external and thus the imaging plane may be manually adjustable
through physical adjustment of knobs, pins, levers, or other
mechanical adjustment features. In other embodiments, the mechanism
112 may be internal and the imaging plane may be adjustable
automatically by the controller 102 or manually through provider
interaction with the controller 102.
[0052] In another embodiment, the patient interface 100 can include
a housing 114 enclosing the probe 110 and the probe 110 can be
adjustable within the housing 114. In this embodiment, the variable
imaging plane mechanism 112 results from the interaction of the
probe 110 with the housing 114. For example, the probe 110 can be
rotatably positioned within the housing 114 about an axis
substantially orthogonal to the patient body surface. The housing
114 may include an upper half and a lower half slidably connected
about a circular perimeter allowing the upper half to rotate
relative to the lower half. The probe 110 may be connected to the
upper half allowing for the rotation of the probe 110 via rotation
of the upper half relative to the lower half. The probe 110 can
alternatively or additionally be pivotal about an axis
substantially parallel to the patient body surface. The probe 110
may be positioned on a pivot rod extending from the housing 114
where the pivot rod is pivotally connected to the housing 114. The
pivot rod may include a pivot knob for adjusting the pivotal
position of the pivot rod thereby adjusting the pivotal position of
the probe 110. In other embodiments, the probe 110 can be slidably
positioned within the housing 114 allowing the probe 110 to
translate in one or more directions parallel to the patient body
surface. The probe 110 can be adapted to move in a direction
relative to the housing 114 allowing for adjustability of the
signal being emitted and/or received from the probe 110.
[0053] As shown in FIG. 3, an exemplary external imaging plane
mechanism 112 is shown. As shown, the probe 110 may include a
connecting pad 116, a housing 114 allowing for rotation of the
transducer in a plane substantially parallel to the patient
surface, and a lateral side bar 118 for pivoting the transducer in
elevation. The external imaging mechanism 112 may be adjusted
automatically with a series of controlled actuators and/or the
system may be adjusted manually. In FIG. 4, an exemplary internal
imaging plane mechanism 112 is shown. The mechanism 112 includes a
rotation pulley 120 and cable 122 for rotating the transducer in a
plane substantially parallel to the patient surface and an
elevation pulley 124 and cable 126 for pivoting the transducer
relative to the patient surface. As with the external mechanism
112, the internal mechanism 112 may be adjusted automatically
and/or manually.
[0054] Referring to FIGS. 5-8, the probes 110 of the patient
interface 100 can be positioned on a patient and connected to the
patient with a securing system. The securing system can include a
connecting pad 116 and the probe 110 can be affixed to the
connecting pad 116. Alternatively, the connecting pad 116 can be
omitted and the probe 110 can be adhered or externally secured
directly to the body surface. Additionally, the securing system can
include a probe detection device 128 adapted to trigger activation
and calibration of an attached probe 110. As shown, the probe 110
can be connected to the controller 102 with a lead 115.
[0055] Referring particularly to FIG. 8, the connecting pad 116 can
be an elastomeric material such as rubber or foam rubber.
Preferably, the connecting pad 116 can be a latex free elastomeric
material. The connecting pad 116 can include a single layer or
multiple layers. The connecting pad 116 can include an aperture 130
for receiving a distal end of the probe 110. The aperture 130 can
extend fully through the connecting pad 116 or can extend partially
through the pad 116 as shown. Where the aperture 130 extends fully
through the connecting pad 116, a distal end of the probe 110 can
be placed in direct contact with the patient body surface through
the aperture 130. Preferably, the contact between the probe 110 and
the body surface is free of air voids. In some embodiments, an
ultrasonic gel 131 can be provided between the probe 110 and the
patient body surface as shown in FIG. 2. Where the aperture 130
extends partially through the connecting pad 116, the portion of
the pad 116 between the probe 110 and the body surface can be solid
or a liquid ultrasonic gel type material. Preferably, the portion
of the pad 116 between the probe 110 and the body surface is free
of voids or air pockets.
[0056] The probe detection device 128 can be integrated into the
connecting pad 116. The device 128 may be adapted to sense that a
probe 110 is connected to the pad 116 and may further be adapted to
trigger activation and calibration of the probe 110. The probe
detection device 128 can be in electrical and/or data communication
with the controller 102 and can thus signal the controller 102 when
a probe 110 is present. This communication may be facilitated
through contact with the probe 110. That is, the device 128 may not
be in communication with the controller 102 unless or until the
probe 110 is attached to the connecting pad. Alternatively or
additionally, the device 128 may be in direct communication with
the controller 102 via a wired or wireless connection. In a
preferred embodiment, the probe detection device 128 can be an
electronic chip embedded in the connecting pad 116. The chip can
include a contact or other sensing mechanism, such as a pressure
sensor, for sensing the attachment of a probe 110 to the connecting
pad 116. Upon attachment of a probe 110, the chip may be configured
to signal the controller 102 to activate and calibrate the attached
probe 110. In some embodiments, the connecting pads 116 may be
adapted for use at a particular position or window. In these
embodiments, the chip of the probe detection device 128 may be
designed, configured, or otherwise adapted to indicate its position
to the controller 102 such that the attached probe 110 can be
activated and calibrated for a particular position on the
patient.
[0057] The connecting pad 116 can be secured to the patient with a
securing system. Preferably, the securing system is an adhesive and
more preferably is a biocompatible adhesive. Alternatively or
additionally, the connecting pad 116 can be connected to the
patient with an external system in the form of a superimposed layer
of adhesive material. For example an oversized piece of tape can be
positioned over the probe 110 and the connecting pad 116 to secure
the assembly to the patient. The superimposed adhesive material
could alternatively include a central aperture for receiving the
probe 110 so as to secure the connecting pad 116 to the body
surface without covering the probe 110. The superimposed adhesive
material can include a slit or slot through the portion of the
material around the aperture to allow the material to be positioned
around the lead 115 extending from the probe 110 and allowing the
material to be easily removed and replaced. In yet another
alternative, the external system can be one or more bands, belts,
or straps positioned to secure the probe 110 and/or connecting pad
116 to the patient's body surface. The external system can extend
around the patient's body and be drawn tight or connect to a
supporting table in the form of a tie-down. The external system can
extend across the surface of the probe 110 and/or connecting pad
116 or it can be secured to the probe 110 and/or connecting pad 116
via a hook, a loop, a button, a hook and loop system, or some other
securing mechanism. The external system can connect to itself with
any or a combination of any of the above listed connections.
[0058] The patient interface 100 can be in data communication with
the controller 102 via a lead 115, in the case of a wired
connection, or the patient interface 100 can be in wireless data
communication with the controller 102. Where a wired connection is
provided, the connection can include power flowing to the patient
interface 100 from the controller 102 or the patient interface 100
can includes its own power source. Where wireless communication is
provided, the patient interface 100 can include its own power
source. The power source, in either a wired or wireless condition,
can include probe specific batteries, or an overall patient
interface battery connected to all of the probes 110.
[0059] The probe or probes 110 can be the same or similar to the
probe described in U.S. Provisional Patent Application No.
61/140,767 filed on Dec. 24, 2008 entitled Peripheral Ultrasound
system (apparatus and method) for automated and uninterrupted data
acquisition. The probe or probes 110 can alternatively be the same
or similar to the device described in U.S. Pat. No. 5,598,845 to
Chandraratna et al. The probe or probes 110 can alternatively be
the same or similar to the device described in U.S. Pat. No.
6,261,231 to Damphousse. The probe or probes 110 may alternatively
include features and combinations of any or all of the above
disclosures.
[0060] Referring now to FIGS. 9-10, a provider interface 104 is
shown. The provider interface 104 can include one or more provider
output devices and one or more provider input devices. Regarding
the provider output devices, a display 132 in the form of a
cathode-ray tube (CRT), liquid crystal display (LCD), Plasma based
display, or another type of display 132 can be provided. The
provider output device can also include a printer and can include a
speaker for transmitting sound type output in the form of tones or
verbal output.
[0061] In a preferred embodiment, the display 132 may be large
enough to present clear ultrasound images and image acquisition
sequencing. For example, the display 132 may be adapted to present
four digital loops at the same time as shown in FIG. 10. More or
fewer loops can also be provided. The display 132 may also be
adapted for displaying an EKG signal or a blood pressure value. In
one embodiment, the display 132 can show a value for continuous
left-sided cardiac output. For example, the display 132 may read 5
Liters/min. Additionally, consideration can be given to the
workspace of the provider and as such, the display 132 can be
similar in size to a monitor display on an EKG or a blood pressure
monitor. Other output type devices may be provided.
[0062] Regarding the input devices, a keyboard, mouse, or joystick
can be provided. Additionally, a touchpad can be included or a
microphone for receiving an audio type input can be provided. In a
preferred embodiment, the display 132 output device can double as
an input device via a touch screen for receiving input information
from the provider. Alternatively or additionally, the display 132
may include buttons or switches as shown in FIGS. 9 and 10. Other
input devices can also be used.
[0063] Referring to FIG. 11, the auxiliary device interface 106 can
include one or more ports on the controller 102 for connection of
the auxiliary devices. The ports can be any suitable plug-type
socket on the controller 102 for receiving a lead from an auxiliary
device. Alternatively, the auxiliary device interface 106 can be a
wireless based interface for receiving input information from an
auxiliary device.
[0064] Still referring to FIG. 11, the network interface 108 can
include one or more jacks on the controller 102 for connection to a
network. This jack can be any suitable connection socket on the
controller 102 for receiving a network cable for connection to a
near by network jack. For example, an Ethernet connection jack, USB
port, or phone jack may be provided. Other suitable connection
systems can be provided. The network interface 108 can also include
a wireless based interface for communicating with a wireless
network.
[0065] Referring still to FIG. 11, a controller 102 is shown. The
controller 102 can include a computer adapted to connect and
control several interfaces. Alternatively, the controller 102 can
be more particularly constructed for a particular process or
purpose. The controller 102 can be in the form of a field
programmable gate array, a mixed signal micro controller 102, an
integrated circuit, a printed circuit board, or the controller 102
can be created in a virtual product development platform such as
LabVIEW or the like. Accordingly, the controller 102 can include
any combination of hardware and software and can be adapted for a
particular purpose.
[0066] Processes and analyses performed by the controller 102 can
be performed by modules including hardware, software, or some
combination of hardware and software. In a preferred embodiment,
the controller 102 includes a patient interface module 134, an
analysis module 136, and a provider interface module 138. The
provider interface module 138 may further include a clinical
management module 140, an electronic reporting module 142, and a
Diagnosis Related Group (DRG) reporting module 144. Other modules
can be included and can be adapted for receiving, sending,
interpreting, or analyzing data and any combination of processes
can also be included in any given module.
[0067] The controller 102 can include hardware and/or software to
interact with and control any or all of the several included
modules and/or interfaces. Moreover, any combination of the
software, hardware, and/or modules is within the scope of the
present disclosure. Accordingly, complete or partial overlap of the
functionality of the modules should be understood to exist in
certain circumstances.
[0068] The controller 102 can include a patient interface module
134 adapted to control the patient interface 100. More
particularly, the patient interface module 134 can be adapted to
drive the probes 110. In a preferred embodiment, the patient
interface module 134 may include an image generating module 146.
The image generating module 146 can be adapted to control
ultrasonic transducers and can be adapted to generate, transmit,
and receive ultrasonic waves via the transducers. Accordingly, the
image generating module 146 can perform beamforming, array
beamforming, and all signal processing functions. The image
generating module 146 can produce two-dimensional and
three-dimensional imaging as well as B-mode, M-mode, color Doppler,
and spectral Doppler data points. In the case of alternative or
additional types of probes 110, the patient interface 100 can be
adapted to initiate suitable probe signals and/or receive probe
data.
[0069] In addition, the patient interface module 134 can control
the adjustment of the probe view. That is, where the probe 110 is
adjustable relative to its position on the patient, the patient
interface module 134 can control actuation devices for rotating,
pivoting, translating, or otherwise adjusting the position and
probe view obtained by the probe 110. Alternatively or
additionally, the adjustment of the probes 110 may be manually
performed with knobs or other physical adjustment devices.
[0070] The patient interface module 134 can be adapted to
periodically or continuously collect data via the probes 110 of the
patient interface 100. In a preferred embodiment, the patient
interface module 134 can automatically acquire ultrasound-generated
data points at a selected time interval. For example, the patient
interface module 134 can be set by the provider to obtain
cardiovascular information about a patient every minute, every two
minutes, every 10 minutes, or at any time interval selected by a
provider.
[0071] The patient interface module 134 can also be adapted to
control the manner in which the probes 110 collect the data. That
is, the patient interface module 134 can select from one or more
modes for any given probe 110 to use when collecting information.
For example, a first mode of data collection may include a
two-dimensional (2D) black and white image of the moving heart
muscle and valves, as shown in FIG. 12. In this mode, one or more
heart beat cycles may be acquired for each 2D image cross-section.
The heart beat cycles can be shown on the display 132 in a video
loop format called a 2D clip such that the heart looks to be
beating continuously. A second mode of data collection may include
color Doppler imaging. This mode may also include a region of
interest (ROI) box superimposed on a 2D ultrasound image. The ROI
box may be defined by the provider by clicking and dragging a mouse
to form a box. Other known methods of selecting a box may be used
and other shapes other than a box may also be used. Within the ROI,
the velocity and direction of the blood flow during a cardiac cycle
may be shown using a range of shades of blue and red colors. The
blue and red colors may reflect the direction of flow toward or
away from the probe 110. (i.e., red being toward the probe 110 and
blue being away from the probe 110.) In FIG. 13, the blood flow is
toward the probe and would appear on a color display in red.
Similar to the first mode, this mode may also be shown on the
display 132 in a video loop format. A third mode of data collection
may include spectral Doppler tracings. Similar to the second mode,
this third mode may also use a ROI defined by the provider. The
spectral Doppler may measure and display the direction and velocity
of the blood flow within the ROI as shown in FIG. 14. The spectral
Doppler mode allows calculation of clinically useful volumes,
flows, and pressures using the measured velocities.
[0072] After imaging and acquisition, all ultrasound-generated data
may be recorded and stored in a memory of the controller 102.
Alternatively or additionally, the data may be directly
communicated to the analysis module 136 for further processing. The
memory of the controller 102 may be a digital memory of a hard
drive where a computer system is provided as the controller 102.
Other memory types can be used. The ultrasound-generated
information can allow for determination of the assessment of
ventricular contractility, valvular structure and function, cardiac
output and filling pressures.
[0073] The controller 102 can also include an analysis module 136.
The analysis module 136 can be adapted for use with a specific type
of probe 110 or it may be a more general module adaptable for use
with several, and/or differing types, of probes 110. The analysis
module 136 can use information received from the probes 110 and can
process that information into additional data or results.
[0074] In a preferred embodiment, the analysis module 136 can be
adapted for use with ultrasonic transducer type probes 110. The
analysis module 136 can include one or more algorithms configured
for analyzing the circulatory function information obtained by the
transducers and for developing cardiovascular determinants. These
algorithms may include interpretive processes or more calculated
processes depending on the information received and the
determinants being developed. As discussed above, the information
received may be provided in one of at least three forms including:
a) 2D or 3D black and white images b) Color Doppler images, and c)
Spectral Doppler tracings. The determinants being developed and
used for monitoring patients can include: contractile function,
valvular function, cardiac output, and filling pressures.
[0075] These determinants can be developed by the analysis module
136 through interpretation of one or more types of
ultrasound-generated images and/or calculations based on ultrasound
data. In some cases, for example the cardiac output, the
development of the determinant may be a substantially calculated
process. However, in other cases, for example the contractile
function, the development of these determinants may be a
substantially interpretive process. For example, determining
whether the contractile function is normal requires knowledge of
how a normal contracting heart appears. Accordingly, this
interpretive process may include comparing a captured image clip to
image clips with known values or categorizations. Image recognition
software may be employed for comparing the captured clip to a
series of stored clips. A correlation algorithm for making the
comparison may be based on previously defined visual assessment
pattern correlations, where the visual assessment was performed by
clinical diagnostic experts in cardiac ultrasound imaging and the
clinically adequate and relevant correlation is made possible by
evaluating and computing a large number of cases and images.
Alternatively or additionally, where the provider is viewing the
display 132, the provider may interpret the image or may compare
the image to the database of images. Accordingly, the provider may
develop the determinants separate from and/or in addition to the
system.
[0076] In one embodiment, the correlation algorithm may include
analyzing a captured image clip with an image recognition module
148 and may further include comparing the result to a series of
stored image clips in a database. Each of the stored image clips in
the database may be assigned to a category based on previous
clinical studies as discussed above. A rating may be given to the
comparison of the captured image clip to a respective stored image
clip for each comparison made. The captured clip may be compared to
all of the stored clips and a category may be assigned to the
captured image clip consistent with those image clips to which the
comparison had the highest ratings. Alternatively or additionally,
a trend of a likeness to a given category of stored clips may be
recognized and a category may be assigned accordingly. In either
case, the captured image clip may be categorized consistent with
the stored image clip or clips that it most closely resembles.
Other algorithms may be followed to correlate a captured image clip
with a category of clips in a database and these other algorithms
are within the scope of the present disclosure.
[0077] Regarding the contractile function, the analysis module 136
can develop both right and left contractile function information by
analyzing a 2D and/or 3D captured image clip provided by the
patient interface 100. The captured image clip can be compared to
image clips in a contractile function image clip database and a
category may be assigned to the captured image clip as shown in
FIG. 15. Accordingly, the correlation algorithm may be used to
categorize the acquired 2D image clip into a a) hyperdynamic, b)
normal, c) moderately reduced, or d)severely reduced ventricular
contractile function pattern.
[0078] Regarding the valvular function, the analysis module 136 can
provide an assessment of the presence and severity of mitral,
aortic, and tricuspid valve regurgitation by analyzing color
Doppler images. A color Doppler image clip of these valves can be
captured by the patient interface 100. The analysis module 136 can
compare the image to image clips in respective mitral, aortic, and
tricuspid image clip databases. A category can be assigned to the
captured image clip for each valve. Accordingly, the correlation
algorithm can be used to categorize the valvular function of each
valve as shown in FIG. 15. For the mitral valve, the algorithm may
categorize the captured image clip into a a) mild, b) moderate, or
c) severe mitral regurgitation pattern. For the aortic valve, the
algorithm may categorize the captured image clip into a a) mild, b)
moderate, or c) severe aortic regurgitation pattern. For the
tricuspid valve, the algorithm may categorize the captured image
clip into a a) mild, b) moderate, or c) severe tricuspid
regurgitation pattern.
[0079] Regarding the cardiac output and filling pressures, the
analysis module 136 can utilize spectral Doppler tracings to
determine these and other related values. For example, spectral
Doppler can be used by the analysis module 136 to provide a basic
assessment of the left ventricular diastolic function, the left
ventricular filling pressure, the systolic pulmonary artery
pressure, the presence and severity of aortic stenosis, and the
cardiac output.
[0080] Regarding diastolic function, a spectral Doppler tracing
relating to the mitral inflow (i.e., the mitral inflow tracing) can
be used to obtain an image clip with the patient interface 100. The
captured clip can be compared to stored clips in a diastolic
dysfunction image clip database and a category can be assigned to
the captured image clip as shown in FIG. 15. Accordingly, the
captured image clip can be categorized into a a) mild, b) moderate,
or c) severe diastolic dysfunction pattern.
[0081] Regarding the left ventricular filling pressure, a general
filling pressure determinant can be developed using a spectral
Doppler tracing relating to the pulmonary venous flow. A captured
image can be obtained of the spectral Doppler tracing using the
patient interface 100, a comparison can be made to a database of
filling pressure image clips, and a category can be assigned to the
captured clip as shown in FIG. 15. Accordingly, the captured clip
can be categorized into a a) normal or b) elevated left ventricle
filling pressure pattern. Alternatively or additionally, the
filling pressure can be estimated by calculating the ratio between
two spectral Doppler direct measurements. The peak velocity of the
E wave of the mitral inflow and of the e' mitral annulus wave of
the tissue Doppler may be directly measured using spectral Doppler.
The ratio of the E wave velocity to the e' mitral annulus wave
velocity can provide a numerical estimate of the left ventricular
filling pressure. Once calculated, the filling pressure can be
numerically compared to known normal pressures. For example,
approximately 5-15 mm Hg may be considered normal and values above
or below this range may be deemed high or low respectively.
[0082] Regarding the systolic pulmonary artery pressure, a spectral
Doppler tracing of the velocity of the red cells of the systolic
tricuspid regurgitation jet may be obtained by the patient
interface 100. A direct measurement of the peak velocity may
provide a clinically relevant estimation of the systolic pulmonary
artery pressure using the simplified Bernoulli equation. The normal
range of the systolic pulmonary artery pressure may be less than 30
mm Hg.
[0083] Regarding mitral and aortic stenosis, direct measurements
may be made of spectral Doppler tracings to develop these
determinants. For mitral stenosis, the mean gradient of pressure
may be directly measured from the spectral Doppler tracing of the
mitral inflow and the severity of mitral stenosis may thus be
defined as either a) mild (mean gradient of 5 mm Hg), b) moderate
(>5 and <15 mm Hg), or c) severe (>15 mm Hg.) For aortic
stenosis, the peak velocities may be directly measured from the
spectral Doppler tracing of the red cells in the left ventricular
outflow tract (LVOT) and at the aortic valve. The ratio of the peak
velocities of the red cells in the LVOT to those at the aortic
valve may define the severity of aortic stenosis as either a) mild
if the ratio is 1:2, b) moderate if the ratio 1:3, or c) severe if
the ratio is 1:4.
[0084] Regarding the cardiac output, two direct measurements may
lead to the development of this determinant. The profile of the
spectral Doppler tracing obtained from the LVOT during systole may
be used to determine the average distance red cells travel during
this event. That is, the area under the spectral Doppler tracing,
or the integral of the tracing, may provide this average distance.
Additionally, the diameter of the LVOT may be directly measured
allowing for the geometric calculation of LVOT area. With those two
data points, the average distance of red cell travel and LVOT area,
the patient stroke volume and therefore the cardiac output can be
calculated. A normal cardiac output may be from 5 to 6 L/min.
[0085] The controller 102 can also include a provider interface
module 138 for receiving instructions from the provider and for
displaying patient interface 100 or analysis data. The provider
interface module 138 can include software and/or hardware suitable
for receiving and interpreting information from several input
devices such as a mouse, keyboard, touch screen, joystick, or other
input devices. In the case of audio input, the provider interface
may include a voice recognition software for interpreting provider
commands. The provider interface module 138 can include a display
module 150 including software and/or hardware for displaying
graphs, images, text, charts, or other displays for review and/or
interpretation by a provider or other user. Other software and/or
hardware can be provided for other output types such as printing.
In a preferred embodiment, the display module 150 can include
software and/or hardware for a series of menus accessible by the
provider for producing reports, medical record data, billing
information, and other output types.
[0086] In a preferred embodiment, the display module 150 can be
adapted for producing image displays adapted to display anatomy
scanned by the probes 110. That is, the display module 150 can be
adapted to show the data obtained from the several modes of
operation of the probes 110. In a preferred embodiment, the probes
110 produce ultrasound data and the ultrasound-generated data may
be displayed on the monitor as standard ultrasound images. As shown
in FIGS. 10 and 12, the 2D cross-section images may be black and
white moving clips of the heart beating. The images may be looped
video clips giving the end-user the appearance of a continuous
heart beating. As shown in FIG. 13, the color Doppler images may be
2D cross-section images with a ROI color box superimposed on a
valvular structure and showing the direction and velocity of the
blood flow based on the shade and color displayed. This image may
also be a looped video clip showing the heart beating. As shown in
FIG. 14, the spectral Doppler tracings may be still images
displaying a graphical representation of the variation of the
measured red cells velocities over time, usually one cardiac cycle.
In another embodiment, the 2D images may be displayed as 3D images
and provide the equivalent information on ventricular contractility
and valvular structure and function.
[0087] The controller 102 can include a clinical management module
140. The clinical management module 140 can be adapted to receive
data from the analysis module 136 and/or the provider interface
module 138 and present suggested clinical strategies to the
provider. The clinical management module 140 can be based upon
knowledge and studies conducted regarding suitable clinical
management of patients. For example, the clinical management module
140 can include suggested clinical strategies relating to a
particular system of the human body, such as the nervous system,
digestive system, or circulatory system. The clinical management
module 140 can alternatively or additionally include suggested
clinical strategies relating to particular organs or conditions.
Strategies relating to other aspects of patients requiring clinical
management can be included and the clinical management module 140
can be directed to one or more of these aspects of patient
management. Accordingly, the clinical management module 140 can be
adapted to provide a menu or other selection screen allowing for
the focusing of the device for a particular clinical
management.
[0088] In a preferred embodiment, the clinical management module
140 can be directed toward managing the anesthesia or hemodynamic
status of a patient. Preferably, the clinical management module 140
can be adapted for use while the patient undergoes an anesthetic,
perioperative, or critical care procedure. Accordingly, the
clinical management module 140 can be adapted for use with the
analysis module 136 and patient interface 100 described above. The
clinical management module 140 can receive ultrasound or other data
from the analysis module 136 and provide a suitable clinical
management strategy. Alternatively or additionally, the data can be
provided by the provider upon interpretation of the ultrasound
generated images and/or data.
[0089] In the preferred embodiment, the clinical management module
140 may use the cardiac output and the left ventricular filling
pressures as first order data points to manage a patient's
hemodynamic status. Additionally, the clinical management module
140 may use the valvular function and the biventricular contractile
function as second order data points to manage a patient's
hemodynamic status. The clinical management module 140 can assess
the primary and/or secondary order data points and suggest a
suitable clinical strategy. The clinical strategy may suggest the
adjustment of one or more cardiovascular determinants. In
particular, the strategy may suggest the adjustment of
cardiovascular control determinants such as the preload, the
afterload, the heart rate, and the ventricular contractility. The
clinical strategy can be followed by the provider or the provider
may choose not to follow the strategy.
[0090] As shown in FIG. 16-25, the clinical management module 140
can include one or more algorithms to be followed based upon the
input information provided. Referring to FIG. 16, in clinical cases
where the first order data points 200 indicate a low cardiac output
202 and high filling pressure 204, the clinical management module
140 may suggest that the provider reduce the preload 206 and reduce
the afterload 208 (Strategy 1). Referring to FIG. 17, where the
first order data points 200 indicate a low cardiac output 202 and
filling pressure 204 within normal limits, the module may suggest
that the provider reduce the afterload 208 and maintain the current
preload 206 (Strategy 2). In FIG. 18, the first order data points
200 indicate a low cardiac output 202 and low filling pressure 204
and the strategy suggests that the provider increase the preload
206 (Strategy 3). In FIG. 19, the first order data points 200
indicate a normal cardiac output 202 and high filling pressure 204
and the strategy suggests that the preload 206 be reduced and that
the systemic blood pressure be maintained if within normal limits
(Strategy 4). The strategy may also suggest that the afterload 208
be reduced if the systemic blood pressure is high (Strategy 4).
Referring to FIG. 20, where the first order data points 200
indicate a normal cardiac output 202 and normal filling pressures
204, the strategy may be to maintain the current preload 206 and
afterload 208 conditions (Strategy 5). As shown in FIG. 21, in
clinical cases where the cardiac output 202 remains low despite
optimal preload 206 and afterload 208 management and the second
order ultrasound-generated data points 210 indicate a reduced
contractile function 212, the strategy may be made to use inotropic
support 214 (Strategy 6).
[0091] Referring now to FIG. 22, where the second order data points
210 indicate mitral valve regurgitation 216, the strategy may be to
reduce the afterload 208 and maintain a faster heart rate 220 and
higher preload 206 (Strategy 7). Where mitral valve stenosis 218 is
indicated, the strategy may be to reduce the preload 206 and
maintain a slower heart rate 220 (Strategy 7). Referring to FIG.
23, where the second order data points 210 indicate aortic valve
regurgitation 222, the strategy may include reducing the afterload
208 and maintaining a faster heart rate 220 and higher preload 206
(Strategy 8). As shown in FIG. 24, in clinical cases where the
second order data points 210 indicate aortic valve stenosis 224
with high filling pressures 204, the strategy may suggest to reduce
the preload 206 and maintain a slower heart rate 220 (Strategy 9).
As shown in FIG. 25, where the second order data points 210
indicate aortic valve stenosis 224 with normal filling pressures,
the strategy may be to maintain a slower heart rate 220 and the
module may also include an indication that afterload 208 reduction
is safe (Strategy 10).
[0092] Referring now to FIGS. 26 and 27, clinical management
strategies are shown with additional detail. Moreover, these
strategies are shown to interface with a conventional parameter
such as systolic blood pressure 226. With reference to FIG. 26,
where the first order data points 200 indicate that the cardiac
output 202 is low the clinical management module 140 can then look
to the additional first order data point, filling pressure 204, to
determine which of two branches to follow for determining a
clinical strategy. Where the filling pressure 204 is high, three
additional branches are based upon systolic blood pressure 226. For
a systolic blood pressure (BP) 226 greater than 120 mm Hg, the
clinical strategy may suggest reducing the afterload by 15% and
limiting intravenous fluid (IV) as required to keep the vein opened
(KVO). For a systolic BP 226 of 90 to 120 mm Hg, the clinical
strategy may suggest reducing the afterload by 10% and limiting the
IV preload to KVO. For a systolic BP 226 less than 90 mm Hg, the
clinical strategy may suggest limiting the IV preload to KVO and to
consider inotropic support. Similarly, where the filling pressures
are normal, three additional branches also based on systolic BP 226
are shown. Where systolic BP 226 is greater than 120 mm Hg the
clinical management strategy may be to reduce the afterload by 15%
and maintain basal IV fluid intake. For a systolic BP 226 of 90 to
120 mm Hg, the clinical strategy may suggest to reduce the
afterload by 10% and maintain basal IV fluid intake. Where systolic
BP 226 is less than 90 mm Hg, the clinical strategy may suggest
limiting the afterload reduction. A normal ejection fraction (EF)
may be considered to be from 55% to 70% and in this case if the EF
is greater than 40% the strategy may suggest that the provider
consider an IV bolus of 250 ml. If the EF is less than 40%, the
strategy may suggest that the provider consider inotropic support
and if there is no increase or minimal increase in Stroke volume
(SV), the strategy may further suggest that the provider consider
an IV bolus of 100 ml.
[0093] A similar strategy to that shown in FIG. 26, is shown in
FIG. 27 where the cardiac output 202 is normal. Here, the strategy
differs from that shown in FIG. 26, in the normal filling pressure
204 branch. That is, in the normal filling pressure 204 branch,
where the systolic BP 226 is greater than 120 mm Hg, the strategy
suggests an afterload reduction of 10% in lieu of 15%. Also, for a
systolic BP 226 of 90 to 120 mm Hg, the strategy suggests
maintaining the afterload and the basal IV intake levels in lieu of
reducing the afterload by 10% with maintained basal IV intake
levels.
[0094] It is noted that the present disclosure is not to be limited
to the specific percentages of reductions or increases shown and
described. The reductions and increases in cardiovascular control
determinants have been provided here as examples and do not reflect
an exhaustive list of the available adjustments in the
cardiovascular determinants. For example, the afterload reductions
shown include reductions of 10% and 15%. The afterload reduction
may range from approximately 0% to approximately 50% and preferably
ranges from approximately 10% to approximately 20%. Additionally,
in cases of sepsis or systemic infection, the afterload may be
maintained or increased.
[0095] Additionally, the exemplary strategies shown are not an
exhaustive list. For example, FIGS. 26 and 27 are based solely on
cardiac output 202, filling pressure 204, and systolic BP 226.
Other strategies can be included and can be based on any
combination of cardiovascular determinants. The strategies can be
further based on clinical experience and testing shown to bring
cardiovascular functions closer to normal ranges.
[0096] The controller 102 can include an electronic reporting
module 142. The electronic reporting module 142 can be adapted to
facilitate the development of a report 145 for record keeping or
other purposes. The report 145 compiled by the electronic reporting
module 142 can include the clinical findings relating to patient
condition and can also include the intervention measures taken to
adjust, stabilize, or otherwise change the patient's condition. The
electronic reporting module 142 can be adapted to prompt the
provider with one or more report input screens 143 allowing the
provider to select, confirm, modify, or otherwise tailor the report
145 and can also compile the report based on this input from the
provider. The electronic reporting module 142 can be accessible via
one or more of the input devices of the provider interface 104.
That is, a menu button on the display 132 can be available for
activating the electronic reporting module 142 and the menu button
can be selected via a mouse, a touch screen, or any other input
device. Other suitable activation elements and methods can be
included such as a tab selection, a drop down box, and the
like.
[0097] In a preferred embodiment, the electronic reporting module
142 can be adapted to compile an electronic and/or printed medical
report. Preferably, the report 145 can include information relating
to the hemodynamic management of a patient. Accordingly, as shown,
for example in FIG. 28, the electronic reporting module 142 can
prompt the provider with one or more report input screens 143. The
screens 143 can prompt the provider for input relating to one or
more of the clinical findings obtained by the analysis module 136
and/or intervention measures taken by the provider. The findings on
any particular screen or screens 143 can include, the cardiac
output, the filling pressures, the valvular structure and function,
and the contractile function. Additionally, the screens can include
intervention measures such as adjustments in the afterload,
preload, heart rate, and contractility. Other findings or
intervention measures can be included on the screens.
[0098] As shown, in FIG. 28 for example, the report input screen
143 can be directed to the left-sided cardiac output. The screen
may list a series of options suitable for the particular finding or
intervention measure being addressed. Each of the options may
include a short descriptive sentence representing a more detailed
description of a clinical finding or an intervention measure. The
selection of a report item can be in the form of radio buttons as
shown or the selection can be check boxes, highlights, or other
known selection types. The module 142 can be configured to allow
only one selection or it can allow multiple selections for any
given report item.
[0099] For each finding or intervention, the electronic reporting
module 142 can make an initial selection for reporting based on
information from the analysis module 136. That is, for example, if
the analysis module 136 found that the LVOT was mildly decreased,
the reporting module 142 can make an initial selection for
confirmation or modification by the provider. If the provider has
information indicating that the LVOT was something other than
mildly decreased, the provider can select the appropriate finding.
In the case of intervention measures, for example, if the clinical
management module 140 suggested a preload reduction, the reporting
module 142 may make an initial selection of preload reduction.
However, if the actual intervention measure taken was not to adjust
the preload, the provider can change the selection to, for example,
maintain preload. In some embodiments, the module 142 can omit the
initial selection and allow the provider to select the appropriate
finding or intervention. It is noted, that the report input screens
143 can be directed to clinical findings or intervention measures
not obtained or suggested, respectively, by the system. In these
cases, the initial selection may be omitted. Where a common finding
or intervention measure is known, the system can be configured to
select the common finding or measure as a default for further
review by the provider.
[0100] Upon selection or verification of the appropriate finding or
intervention measure, the provider can be prompted to continue.
Alternatively, the selection or verification can automatically
cause the module to continue. The provider can be prompted with
additional displays as required to select, verify, or otherwise
obtain all of the necessary information for the report 145. Once
complete, the electronic reporting module 142 can compile a
suitable report 145. For example, as shown in FIG. 29, the report
145 can include the detailed descriptions of each of the clinical
findings or intervention measures taken and can also include a
summary of the procedures.
[0101] The compiled report 145 can be in electronic form in a
database report format, a word processing format, or another
format. The report 145 can be saved, printed, or otherwise stored
as a record. The report 145 can be formatted to comply with the
medical record bylaws of a particular healthcare facility or series
of facilities. In addition, the report 145 may be electronically
coded according to Hospital Language (HL) protocol and sent out as
a patient electronic medical record in a compatible format.
[0102] The controller 102 can include a DRG module 144. Many
healthcare system revenues are determined by the Diagnosis Related
Group (DRG) billing codes resulting from a patient's visit to their
facilities. Each DRG code can be associated with a specific fee for
which the hospital can be reimbursed relating to a specific
rendered healthcare service. Most DRG codes have two formats: a
basic DRG and a DRG with complications and comorbidities (CCs). DRG
codes associated with clearly documented CCs are typically
reimbursed at a higher rate than those without CCs (i.e., a basic
DRG). In the event that CCs are adequately identified and
documented, reimbursement at the higher, DRG with CCs, rate is
possible. In addition, identification of CCs at the time of
admission of the patient to the healthcare facility allows for the
documentation of cardiac comorbidities as Present On Admission
(POA), as opposed to a post-operative complication diagnosis. This
may reduce the likelihood of lower reimbursement that is now tied
to the pay-for-performance Medicare and other insurance carrier
programs. The device described herein allows identification of
cardiovascular complications and comorbidities and as such may
allow for early identification of conditions and thus a higher rate
of reimbursement.
[0103] The DRG module 144 may allow for the documentation of
identified CCs. When activated by the healthcare provider, the DRG
module 144 may display a list of International Classification
Diseases (ICD) codes describing cardiovascular CCs capable of being
identified by the device. This list may be displayed on the display
132 as described above and as shown, by way of example, in FIG. 30.
By selecting the most appropriate diagnosis (ICD codes) identified
by the device, the end-user may generate a series of billing codes
that may be used by the healthcare facility to document the CCs.
The billing codes may be documented in a separate report called the
DRG optimization report 147 as exemplified in FIG. 31. The report
147 may be printed on paper or written in an electronic document.
The report 147 may be added to the patient paper or electronic
medical record. The report 147 may also be sent by paper and or
electronically to the healthcare facility billing and coding
department as a separate document from the medical record. This
report 147 may improve the capture of reimbursement for CCs by the
healthcare facility billers and coders for optimization of the
patient's final DRG code submitted to the insurance company for the
services rendered. The billing codes generated may also be used in
a separate document called a professional billing claim 149 as
shown, by way of example, in FIG. 32. This document may allow for
the healthcare provider to be paid for the professional services
rendered with use of the device according to the Current Procedural
Terminology (CPT) code fee schedule.
[0104] Referring now to FIGS. 33-36, the system methodology may be
described. The system can function to acquire data from patients
for use in managing the patient's condition and may further be used
as a reporting tool. Using the patient interface 100, the system
may be adapted to obtain patient information relevant to a
particular procedure or condition. The system can be further
adapted to analyze and/or display that information. In addition,
the system can suggest a suitable clinical strategy for managing
the condition of the patient.
[0105] In a preferred embodiment, the probes 110 of the preferred
patient interface 100 described, can be used to obtain
cardiovascular function information from a patient. The probes 110
may obtain information based upon their position on the patient.
That is, certain positions can represent a cardiovascular window as
described above and can lend themselves toward collection of
particular items of cardiovascular information. Accordingly, in a
preferred embodiment, each probe 110 may have a particular set of
data collection allocated to it based on the particular window it
is positioned in. However, depending on patient anatomy and other
factors, a probe 110 in any given position may not be able to
access the information typically available from its respective
position. In these cases, other positions can be used to compile
the most complete set of data available.
[0106] More particularly, in a preferred embodiment, the basic
sequence of data acquisition may occur through the use of two
probes 110. That is, in some embodiments, two probes 110 may be
able to collect all of the cardiovascular function information by
allocating some of the information to a first probe 110 and the
remaining information to the second probe 110. In other
embodiments, two probes 110 may not be sufficient due to
obstructions or other intervening causes. In still other
embodiments, additional probes 110 may be used to get additional
information by viewing particular structures from additional views.
In some embodiments, a single probe 110 may be sufficient. In other
embodiments, any number of probes 110 may be used.
[0107] Referring to FIG. 33, in a preferred embodiment, a first
probe 110 can be secured on a patient's chest at the parasternal
window 300. This probe 110 may be set by the patient interface
module 134 to a first mode for a 2D black and white image. The
patient interface module 134 can adjust the probe 110 to acquire a
parasternal long-axis 2D imaging cross-section 302 of the heart for
one or more heart beats. This black and white 2D image clip can
show the left ventricular heart muscle contracting and the mitral
and aortic valves open and close. From the same 2D cross-section,
for example, without adjusting the view of the probe 110, the mode
of the first probe 110 can be changed to a second mode and a color
Doppler ROI box may be superimposed on the aortic 304 and mitral
306 valves 2D live image. A clip of the data may be acquired for
one or more heart beats. The color Doppler allows the assessment of
the valves functionality by revealing the blood flow through the
valves. Still using the first probe 110, additional data may be
acquired by adjusting the probe 110 from the parasternal long-axis
2D imaging cross-section 302 to a parasternal short-axis 2D imaging
cross-section 308 for one or more heart beats. This short-axis
probe view 308 can allow for the assessment of the left ventricular
contractile function and volume status.
[0108] Referring to FIG. 34, in a preferred embodiment, a second
probe 110 can be secured on the patient's chest at the apical
window. This second probe 110 can be set by the patient interface
module 134 to a first mode for a 2D black and white image. The
patient interface module 134 can adjust the second probe 110 to
acquire an apical four-chamber 2D imaging cross-section 312 for one
or more heart beats. This 2D clip can evaluate the right and left
ventricular contractile function, as well as the mitral and
tricuspid valve. This additional 2D clip allows for the
three-dimensional heart structure to be assessed by a series of
two-dimensional cross-sections by relying on view from several
angles. The probe 110 can be set to a second mode for a color
Doppler image of the mitral 313 and tricuspid valve 315. From the
same 2D cross-section, for example, without adjusting the view of
the probe 110, the mode of the first probe 110 can be changed to
the third mode and a pulsed-wave spectral Doppler ROI box may be
superimposed on the open mitral valve 314 to measure the velocity
of the red cells coming into the heart during diastole. The data
may be acquired and displayed on a spectral graph showing velocity
over time. The same pulsed-wave spectral Doppler ROI box, for
example, without changing the size of the ROI box, may be
superimposed on the right upper pulmonary vein 316. The
velocity/time spectral graph of the pulmonary venous flow may then
be acquired. The pulsed-wave spectral Doppler ROI box may also be
superimposed on the septal or lateral side of the mitral valve
annulus 318 to measure the tissue Doppler velocities of the left
ventricle. Those three spectral Doppler measurements may then be
used to assess the left ventricular diastolic function and filling
pressure. Also, a continuous wave Doppler sampling of the tricuspid
regurgitation jet 319 peak velocity may be made to estimate the
right ventricular/pulmonary artery pulmonary pressure.
[0109] In a preferred embodiment, the patient interface module 134
can set the second probe 110 back to mode 1 and adjust the second
probe 110 to acquire a 2D cross-section called an apical long-axis
320 for one or more heart beats. From the same apical long-axis 2D
cross-section, patient interface module 134 can set the second
probe 110 to the 3.sup.rd mode and a pulsed-wave spectral Doppler
sampling area may be superimposed on the left ventricular outflow
tract (LVOT) 322 to measure the velocity of the red cells being
ejected out of the left heart over a cardiac cycle (left-sided
cardiac output). Additionally, a continuous-wave spectral Doppler
may be directed in the same longitudinal axis to measure the
velocity of the red cells at the level of the aortic valve 324.
This additional velocity allows the evaluation and quantification
of aortic valve stenosis.
[0110] As mentioned, in some embodiments, the information gathered
from the first and second probes 110 may be insufficient due to
obstructed views or other intervening causes or additional views
may be desired. Referring to FIG. 35, in some embodiments, a third
probe 110 can be secured on the patient's upper abdomen under the
right costal ridge in the sub-costal window. The patient interface
module 134 can set the third probe 110 to a first mode for a 2D
black and white image. The patient interface module 134 can adjust
the third probe 110 to acquire a sub-costal four chamber 2D imaging
cross-section 326 for one or more heart beats. This 2D clip may
evaluate the right and left ventricular contractile function, the
size of the inferior vena cava as well as the mitral and tricuspid
valve. From the same 2D cross-section, the patient interface module
134 can set the third probe 110 to a second mode and a color
Doppler region of interest (ROI) box may be superimposed on the
mitral valve 328 and the tricuspid valve 329. A clip of the data
may be acquired for one or more heart beats. The color Doppler can
allow the assessment of the mitral and tricuspid valve
functionality. In the present embodiment, and still using the third
probe 110, the patient interface module 134 can set the third probe
110 to a first mode. The third probe 110 can be adjusted for a
sub-costal right ventricular inflow-outflow 2D imaging
cross-section 331, which may be acquired for one or more heart
beats. This allows the evaluation of the right heart structures and
function. From the same 2D cross-section, the patient interface
module 134 can set the third probe 110 to a third mode and a
pulsed-wave spectral Doppler sampling area may be superimposed on
the right ventricular outflow tract (RVOT) 332 to measure the
velocity of the red cells being ejected out of the right heart over
a cardiac cycle (right-sided cardiac output). Still using the third
probe 110, a sub-costal LV short-axis 2D imaging cross-section 330
may be acquired for one or more heart beats. This allows the
assessment of the left ventricular contractile function and volume
status.
[0111] When the ultrasound-generated data points from the second
probe 110 regarding the left heart cardiac output are inadequate or
when additional views are desired, the user may rely on a fourth
probe 110 to acquire a continuous-wave spectral Doppler tracing
signal of either the ascending aorta or the distal aortic arch or
the descending aorta.
[0112] When the ultrasound-generated data points from the first,
second, third, or fourth probes 110 are inadequate or as an
additional available set of data, a fifth probe 110 can be used.
Referring to FIG. 36, the fifth probe 110 may be positioned in the
mid-esophageal window and may acquire ultrasound-generated data
points from behind the heart (inside the body). The fifth probe 110
may acquire a mid-esophageal four chamber 2D imaging cross-section
334 for one or more heart beats. This 2D clip evaluates the right
and left ventricular contractile function, as well as the mitral
and tricuspid valves. From the same 2D cross-section, a color
Doppler region of interest (ROI) box may be superimposed on the
mitral 336 and tricuspid 338 valves 2D live image. A clip of the
data may also be acquired for one or more heart beats. The color
Doppler allows the assessment of the mitral and tricuspid valve
functionality. From the same 2D cross-section, a pulsed-wave
spectral Doppler sampling area may be superimposed on the opened
mitral valve 340 to measure the velocity of the red cells coming
into the heart during diastole. The data may be acquired and
displayed on a spectral graph showing velocity over time. Then, the
same pulsed-wave spectral Doppler sampling area may be superimposed
on the left upper pulmonary vein 342. The velocity/time spectral
graph of the pulmonary venous flow may then be acquired. The
pulsed-wave sampling Doppler may then be superimposed on the septal
or lateral side of the mitral valve annulus 344 and may measure the
tissue Doppler velocities of the left ventricle. Those three
spectral Doppler measurements may be used to assess the left
ventricular diastolic function and filling pressure. A continuous
wave Doppler sampling of the tricuspid regurgitation jet 339 peak
velocity may be made to estimate the right ventricular/pulmonary
artery pulmonary pressure.
[0113] The method resulting from the use of the described device
may be referred to as Echocardiography-Guided Anesthesia Management
(EGAM) and/or Echocardiography-Guided Hemodynamic Management
(EGHEM). EGAM/EGHEM may automatically acquire ultrasound-generated
real-time data points like cardiac output and filling pressures to
assess, manage, modify and optimize the patient cardiac preload,
afterload, heart rate and contractility. Two clinical case studies
were conducted as described below.
CLINICAL EXAMPLE 1
Step 1: Patient Selection
[0114] Male patient, 81 year old, scheduled for a left hip pinning
for a fracture repair. He weighs 89 Kg and is 178 cm tall. His BSA
is 2.1 m2. The patient has long-standing hypertension, and has a
history of transmural myocardial infarction (MI) 4 years prior. The
patient has a limited functional capacity of approximately 5 METs
with symptoms of shortness of breath (SOB), occasional chest pain
stable for last two years, and hip pain. His medication includes an
ACEI and a beta-blocker.
Step 2: Baseline Pre-Operative Assessment
[0115] The device and methods previously described in this document
were applied to this patient. This process was performed at bedside
before anesthesia was provided. The process was pain free and took
a few minutes to complete. Below is the summary of the information
provided by the device:
[0116] Baseline Vital Signs: [0117] a. blood pressure (BP)=160/85
mmHg, [0118] b. heart rate (HR)=82 bpm, regular, [0119] c.
SpO.sub.2=92% room air.
[0120] Primary EGAM/EGEM Findings: [0121] a) Reduced cardiac
output: LVOT diameter is 2 cm, LVOT VTI=12 cm. CO: 3.1 L/min,
CI=1.5 Lmin/m.sup.2 [0122] b) LV Filling pressures are elevated
based on a pseudonormal LV filling pattern, a pulmonary venous flow
diastolic dominant and an E/e' ratio of 25.
[0123] Secondary EGAM/EGHEM Findings; [0124] a) Mitral valve: mild
regurgitation. [0125] b) Aortic valve: sclerosis without
significant stenosis. [0126] c) LV contractile function: moderately
reduced with a visually estimated ejection fraction (EF) at
30%.
Step 3: Management Strategies
[0127] The patient presents a low cardiac output, high filling
pressure, high systemic blood pressure, reduced LV contractile
function and mild mitral regurgitation. The suggested EGAM/EGHEM
strategy based on FIG. 26 recommendation is to reduce the afterload
and blood pressure by 15% and limit all IV intakes only to keep the
vein open. A general anesthetic is planned with IV induction agents
and maintenance done with an inhalational agent. If required, the
basal IV intake needs are 65 ml/hour. The EGAM/EGHEM data will be
controlled 5 minutes after induction.
Step 4: Ongoing Intra-Operative Assessment
[0128] The following table summarizes the intra-operative findings
and interventions
TABLE-US-00001 Cardiac Filling Blood LV Timeline output pressure
pressure contractility Interventions Baseline 3.1 High 160/85 EF =
30% Limit preload L/min E/e' = 25 Reduce to systolic BP to 136 5
min post- 3.5 High 132/78 No change Limit preload induction L/min
E/e' = 20 Reduce BP to 112 Control #1 3.8 Normal 108/72 Mild
increase Maintain 15 min later L/mi E/e' = 13 basal needs Reduce BP
to 98 Control #2 4.2 Normal 96/68 No change Maintain 15 min later
L/min E/e' = 12 basal needs Reduce BP to 90 Control #3 4.4 Normal
84/62 EF = 35% Give IV bolus 7 min later L/min E/e' = 10 100 ml
Limit afterload reduction Control #4 4.5 Normal 92/64 No change
Maintain 5 min later L/min E/e' = 14 basal needs Maintain afterload
Control #5 4.3 Normal 96/68 No change Maintain 15 min later L/min
E/e' = 12 basal needs Maintain afterload Control #6 3.8 Normal
145/72 No change Maintain In recovery L/min E/e' = 14 basal needs
room Reduce BP to low 90's
Follow-Up Events
[0129] The case lasted for about 1 hour. The patient received a
total of 250 ml of IV fluid. The urine output during the procedure
was 150 ml. The blood loss was estimated at 150 ml. The SpO2 on
room air in recovery room as well as post-op day 1 was 98%. The
patient remained comfortable. The post-operative course included an
increase of blood pressure medication and the addition of a low
dose diuretic, as well as a reduced salt and fluid intake. The
target systolic BP was in the 90's. The discharge weight was 83 kg,
the CO was 4.3 L/min, BP=96/72. The patient tolerated those changes
well and reported no orthostatic hypotension, no stroke, and no
changes of renal function. He was still alive and doing well at 30
days post-op and did not require readmission during the same period
and had no new cardiac events.
[0130] The device effectively identified that the patient was in a
non compensated state of congestive heart failure with reduced
cardiac output and ventricular contractility. The clinical strategy
used to address those issues was significantly different than what
the standard pre-operative evaluation was dictating because the
supplemental information provided by the device suggested a
completely opposite strategy. By using the invention, the health
care provider had access to more accurate information, was able to
provide better care to the patient and reduce the risk of
post-operative cardiovascular complications.
Case Study 2
Step 1: Patient Selection
[0131] Female patient, 82 year old, scheduled for elective, right
hemicolectomy. She weights 79 Kg and is 160 cm tall. Her BSA is 1.9
m2. Patient has medically treated hypertension with a
hydrochlorothiazide. She stopped smoking two year ago but has a 20
pack-years history. She is complaining of a progressive shortness
of breath and reduction of her functional capacity over the last
year, currently estimated at 6 or 7 METs. She has no chest pain or
palpitations.
Step 2: The Baseline Pre-Op Assessment
[0132] The device and methods previously described in this document
were applied to this patient. This process was performed at bedside
before anesthesia was provided. The process was pain free and took
a few minutes to complete. Below is the summary of the information
provided by the device:
[0133] Baseline Vital Signs: [0134] a. blood pressure (BP)=168/92
mmHg, [0135] b. heart rate (HR)=70 bpm, regular, [0136] c.
SpO.sub.2=90% room air.
[0137] Primary EGAM/EGHEM Findings: [0138] a) Normal cardiac
output: LVOT diameter is 2 cm, LVOT VTI=22 cm. CO: 4.8 L/min,
CI=2.5 L/min/m.sup.2 [0139] b) LV Filling pressures are elevated
based on a restrictive filling pattern, a pulmonary venous flow
diastolic dominant and an E/e' ratio of 35.
[0140] Secondary EGAM/EGHEM Findings: [0141] a) Mitral valve: mild
to moderate regurgitation. [0142] b) Aortic valve: sclerosis with
mild stenosis. [0143] c) LV contractile function is normal with a
visually estimated EF at 60%
Step 3: Management Strategies
[0144] The patient presents a normal cardiac output, high filling
pressure, high systemic blood pressure, a normal LV contractile
function, mild to moderate mitral regurgitation and mild aortic
stenosis. The suggested EGAM/EGHEM strategy based on FIG. 27 is to
reduce the afterload and blood pressure by 15% and limit all IV
intakes only to keep the vein open. A general anesthetic is planned
with IV induction agents and maintenance done with total
intravenous anesthetics agents. If required, the basal IV intake
needs are 60 ml/hour. The EGAM/EGHEM data will be controlled 5
minutes after induction.
Step 4: Ongoing Intra-Operative Assessment
[0145] The following table summarizes the intra-operative findings
and interventions
TABLE-US-00002 Cardiac Filling Blood LV Timeline output pressure
pressure contractility Interventions Baseline 4.8 High 162/92 EF =
60% Limit preload L/min E/e' = 35 Reduce to systolic BP to 145 5
min post- 5.1 High 141/72 No change Limit preload induction L/min
E/e' = 30 Reduce BP to 120 Control #1 5.5 High 128/67 No change
Limit preload 15 min later L/min E/e' = 26 Reduce BP to 110 Control
#2 5.3 High 105/59 No change Limit preload 15 min later L/min E/e'
= 24 Reduce BP to 95 Control #3 5.4 High 92/55 No change Limit
preload 15 min later L/min E/e' = 22 Maintain afterload Control #4
5.2 Normal 96/58 No change Maintain 15 min later L/min E/e' = 14
basal needs Maintain afterload Control #5 5.3 Normal 98/64 No
change Maintain 15 min later L/min E/e' = 12 basal needs Maintain
afterload Control #6 4.8 Normal 78/48 No change Give IV bolus 15
min later L/min E/e' = 10 of 250 ml Maintain afterload Control #7
5.1 Normal 105/74 No change Maintain In recovery L/min E/e' = 14
basal needs room Reduce BP to 90's
Follow-Up Events
[0146] The case lasted for about 2 hours. The patient received a
total of 300 ml of IV fluid. The urine output during the procedure
was 450 ml. The blood loss was estimated at 250 ml. The SpO2 on
room air in recovery room was 97%. The patient remained
comfortable. The post-operative course included an increase of his
existing blood pressure medication and the addition of an ACEI, as
well as low sodium diet. The target systolic BP was in the 90's.
The discharge weight was 72 kg, the CO was 5.2 L/min, BP=100/68.
The patient tolerated those changes well and reported no
orthostatic hypotension, no stroke, and no changes of renal
function. She was still alive and doing well at 30 days post-op and
did not require readmission during the same period and no new
cardiac events.
[0147] The device effectively identified that the patient was in a
non compensated state of congestive heart failure with normal
cardiac output and ventricular contractility but very high filling
pressures. The clinical strategy used to address those issues was
significantly different than what the standard pre-operative
evaluation was dictating because the supplemental information
provided by the device suggested a completely opposite strategy. By
using the invention, the health care provider had access to more
accurate information, was able to provide better care to the
patient and reduce the risk of post-operative cardiovascular
complications.
[0148] As shown and described regarding FIGS. 37-42, the system may
perform several methods. The steps included in any of the described
methods may be completed in any order and any or all of the steps
may be included.
[0149] Referring to FIG. 37, a method of is shown including at box
400, Generate ultrasound data point, at box 402, Interpret
ultrasound data points provided by each of the probes 110, at box
404, Rely on a system of first order and second order data points
to suggest an optimal clinical strategy, at box 406, Output the
suggested strategy to a display wherein the strategy includes
modification (increase, reduce or maintain) of one or more
cardiovascular determinants such as preload, afterload, heart rate,
and ventricular contractility, at box 408, Display a list of
possible clinical findings, at box 410, Prompt end-user to select
from a list, at box 412, Receive input from end-user, and at box
414, Generate a Final Report.
[0150] In addition, the method may include at box 416, Prompt user
with a list of ICD codes for selection based on output from system
analysis, at box 418, Receive input from end-user regarding ICD
codes, at box 420, Prepare DRG optimization report, and at box 422,
prepare a professional billing claim.
[0151] Referring to FIG. 38, a method is shown including, at box
424, obtaining ultrasound information regarding a condition of the
patient from an ultrasound probe, at box 426, communicating the
ultrasound information to a controller in communication with the
ultrasound probe, at box 428, employing the controller to develop a
determinant from the ultrasound information reflecting the
condition of the patient, and at box 430, providing on an output
device in communication with the controller a clinical management
strategy based on the determinant.
[0152] Referring to FIG. 39, a method is shown including, at box
432, receiving ultrasound information from a patient interface, the
patient interface being adapted to obtain ultrasound information
related to cardiovascular function status of the patient, at box
434, processing the ultrasound information to determine the
cardiovascular function status of the patient, and at box 436,
sending the status to a clinical management module for the
development of a clinical strategy.
[0153] Referring to FIG. 40, a method is shown including, at box
438, comparing a first order data point to a plurality of
categories, wherein the first order data point is associated with
ultrasound information, at box 440, assigning a category from the
plurality of categories to the first order data point based on
which category of the plurality of categories, the first order data
point falls, at box 442, selecting a recommended intervening
measure based on the assigned category, and at box 444, presenting
the recommended intervening measure on a display.
[0154] Referring to FIG. 41, a method is shown including, at box
446, positioning ultrasound probes on a patient, the ultrasound
probes being in communication with a controller, at box 448, using
an input device to instruct the controller to obtain cardiovascular
function information from the patient via the ultrasound probes, at
box 450, reviewing a suggested clinical management strategy, the
strategy including a recommended intervening measure and being
based upon the ultrasound information, and at box 452, deciding
whether to conduct the recommended intervening measure, a different
intervening measure, or no intervening measure.
[0155] Referring to FIG. 42, a method is shown including, at box
454, monitoring a patient via ultrasound and generating information
with the ultrasound and based upon the information, recording a
clinical finding and recommending and recording an intervening
measure, at box 456, displaying a list of clinical findings
including the clinical finding and related clinical findings, at
box 458, prompting a user to select from the list of clinical
findings, at box 460, displaying a list of intervening measures
including the intervening measure and related intervening measures,
at box 462, prompting the user to select from the list of
intervening measures, and at box 464, compiling a report including
the selected clinical finding and the selected intervening
measure.
[0156] While the term provider has been used throughout the
specification, it is to be understood that this is not limited to a
licensed medical doctor, physicians assistant, nurse practitioner,
and the like. Instead, provider can by any user of the system.
Preferably, the provider is someone working under the guidance of a
licensed practitioner and who understands cardiovascular function
so as to provide suitable input to the system.
[0157] Additionally, while the phrase black and white has been used
with reference to certain ultrasound images, it is to be understood
that black and white means a non-color image. That is, an image
that does not accurately depict the colors of the displayed
elements, but rather displays similar but varying tones of several
elements to make them distinguishable from one another. For
example, black and white, sepia, orange, or green colors may be
included within the black and white description.
[0158] Additionally, the categories of cardiovascular determinants
are not to be limited to those categories disclose. More or less
precise categories could be used and the image clip databases and
categories can be adjusted accordingly. For example, with respect
to contractile function, rather than using hyperdynamic, normal,
moderately reduced, and severely reduced as categories, the
categories could instead be normal and abnormal. The contractile
function image clip database can be adjusted to include normal
clips and abnormal clips and to include only two categories in lieu
of four. This holds true for all of the image clip databases and
the associated categories.
[0159] Although the present invention has been described with a
certain degree of particularity, it is understood the disclosure
has been made by way of example, and changes in detail or structure
may be made without departing from the spirit of the invention as
defined in the appended claims.
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