Optimizing ankle-brachial index measurement for peripheral
arterial disease screening in mobile clinics
Shahida N. Balaparya, EdD, MBA, RVT,a Rosemary G. Cobb, BA,b Jaeyoung Lee, BS,b
Jessica P. Simons, MD, MPH,a Douglas W. Jones, MD, MS,a Andres Schanzer, MD,a and
Tammy T. Nguyen, MD, PhD,a,c Worcester, MA
ABSTRACT
Objective: Multidisciplinary mobile clinics (MMCs) provide a robust venue to provide health care access and peripheral
arterial disease (PAD) screening to underserved populations. The ankle-brachial index (ABI) can facilitate PAD diagnosis;
however, traditional supine ABI measurements may be challenging technically in a mobile outreach clinic with limited
infrastructure, whereas seated ABI offers technical ease. In this study, the usefulness and feasibility of performing supine
ABI, seated ABI, and seated ABI with a calculation to account for seated hydrostatic pressure (seated-adjusted ABI) were
compared in a mobile outreach setting.
Methods: Prospective data were collected from patients at five independent MMCs focused on diabetic foot and PAD
screening with ABI for underserved communities. Three techniques were used to measure the ABI: seated ABI, seatedadjusted ABI using a formula to account for hydrostatic ankle pressure, and traditional supine ABI using a foldable
massage table that is 5% of the cost of a medical stretcher. Comparative analysis was performed using the Student t test
analysis and one-way analysis of variance. The frequency of completed seated ABI, seated-adjusted ABI, and supine ABI
examinations performed at independent MMCs was quantified to determine feasibility.
Results: In 166 individuals experiencing homelessness or housing instability who were screened over the course of five
MMCs, 89 underwent PAD screening with ABI. Of the patients screened, 38 patients had seated, seated-adjusted, and
supine ABIs measured (43% of total number of patients undergoing any ABI measurement). PAD (ABI < 0.9) was
identified in one patient using all three ABI methods. Noncompressible ABI (ABI $ 1.3) were identified in 32 patients (32/
38 [84%]) screened with seated ABI. Of these 32 patients, 24 (75%) continued to have noncompressible ABIs using seatedadjusted ABI. Of these 24 patients, 4 (17%) continued to have noncompressible ABI using supine ABI. The average seated
ABI significantly differed from supine ABI (1.34 vs 1.14; P < .0001). The average seated ABI also significantly differed from
seated-adjusted ABI (1.34 vs 1.29; P ¼ .026). The average seated-adjusted ABI significantly differed from supine ABI (1.29 vs
1.14; P ¼ .0204).
Conclusions: We found that seated and seated-adjusted ABI are grossly inaccurate and more often lead to falsely
elevated noncompressible ABI (32/38 [84%] and 24/38 [75%], respectively) compared with supine ABI (6/38 [16%]). We
recommend using supine ABI on patients for PAD screening. Supine measurement is technically feasible in outreach
mobile clinics using a transportable folding massage table and is a more accurate tool for PAD screening. (JVS-Vascular
Insights 2024;2:100125.)
Keywords: Ankle-brachial index; Peripheral arterial disease screening; Outreach clinic; Mobile clinics; Homelessness
From the Division of Vascular Surgery, Department of Surgery, University of
Massachusetts Memorial Medical Centera; the University of Massachusetts
Chan Medical Schoolb; and the Diabetes Center of Excellence, University of
Massachusetts Chan Medical School.c
Supported through the SVS Foundation Vascular Care for the Underserved Pilot Project grant.
Correspondence: Tammy T. Nguyen, MD, PhD, Division of Vascular Surgery,
Department of Surgery, University of Massachusetts School of Medicine, 55
N Lake Ave, S3-731, Worcester, MA 01655 (e-mail: tammy.nguyen@
umassmemorial.org).
The editors and reviewers of this article have no relevant financial relationships to
disclose per the Journal policy that requires reviewers to decline review of any
manuscript for which they may have a conflict of interest.
2949-9127
Ó 2024 The Author(s). Published by Elsevier Inc. on behalf of the Society for
Vascular Surgery. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
https://doi.org/10.1016/j.jvsvi.2024.100125
Peripheral arterial disease (PAD) is a rapidly growing
health concern affecting >200 million people worldwide
and >8.5 million people in the United States.1,2 Poor PAD
outcomes have been strongly linked to low socioeconomic status, rurality, and non-White race or ethnicity.
Patients who experience limited access to health care
are at higher risk of developing severe forms of PAD leading to major lower extremity amputation3e6 and have
poorer outcomes after amputation.5 However, ensuring
health care access for early PAD diagnosis and prevention in communities with low socioeconomic status,
rurality, and non-White race or ethnicity remains a
challenge.
Mobile health clinics have emerged as a powerful tool
to reach patients most impacted by housing insecurities.
1
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The use of mobile health clinics can be a cost-effective
investment of health care funds7,8 and has been successful in screening patients for PAD among at-risk communities.9,10 Individuals experiencing homelessness and
housing instability have been estimated to have a three
times greater risk of cardiovascular disease vs housed individuals11 with increasing risk associated with the duration of homelessness.12 In 2020 we implemented a
medical-provider-driven mobile multidisciplinary clinic
(MMC) focused on PAD and diabetic foot care in patients
experiencing housing insecurity.13 Optimal management
of vascular disease and diabetic care requires a multidisciplinary approach involving nursing, podiatry, vascular
surgery, and social work.14,15 Our MMCs provided a sustainable methodology for leveraging hospital-based resources to build mobile outreach clinics in partnership
with local community programs to provide multidisciplinary care to communities impacted by housing
insecurities.
The ankle-brachial index (ABI) is a widely used PAD
screening tool because it is a simple, low-cost, and noninvasive test with an estimated sensitivity of 61% and a
specificity of 92% for detecting arterial insufficiency.16
The test uses a blood pressure cuff and Doppler ultrasound imaging to compare the ratio of blood pressure
at the ankle with the blood pressure in the arm at the
level of the brachial artery as a measure of perfusion to
the lower extremities2,17 (Fig 1).2 A low ABI (<0.9) is associated with decreased perfusion to the lower extremities.17,19 In contrast, a high ABI ($1.3) reflects
noncompressible arteries, which may be due to vessel
calcification, a feature that is found commonly in patients with diabetes (Table I).20 This finding can lead to
falsely elevated ABI measurements in patients with diabetes.17,21 Despite this limitation, ABI is a valuable tool
in diagnosing PAD. Incorporating the ABI examination
ARTICLE HIGHLIGHTS
d
d
d
Type of Research: Prospective nonrandomized
study
Key Findings: Seated and seated-adjusted anklebrachial index (ABI) is inferior to supine ABI for peripheral arterial disease screening in a mobile
outreach clinic setting.
Take Home Message: Supine ABI is a feasible
method to screen for peripheral arterial disease
and is more accurate than seated and seatedadjusted ABI measurements.
into a mobile clinic presents several technical challenges.
Outdoor mobile clinic events may be loud, making it
difficult to hear faint Doppler signals. Furthermore, supine ABI testing requires a patient to be flat on a
stretcher or examination table, which may be costly
and logistically difficult to transport in a nonpermanent,
resource-limited community outreach clinic. Therefore,
the option to perform a seated ABI measurement to
screen for PAD is appealing in a mobile outreach clinic
because this method does not require a stretcher or
the patient to be supine. To account for the gravitational
pressure in seated ABI, a mathematical adjustment using a conversion factor that considers the hydrostatic
pressure difference between the arm and ankle in a
seated patient has been reported to provide accurate
ABI measurements in a vascular laboratory setting.18
We hypothesize that using seated ABI adjustment calculations will provide a feasible and accurate PAD
screening method at mobile outreach clinics. In this
study, we compared the usefulness of seated-adjusted
ABI and supine ABI examinations in mobile outreach
clinics. We also examined the feasibility of screening
Fig 1. Ankle-brachial index (ABI) measurement methods. The ABI is measured with blood pressure cuff and
doppler on arm and ankle with patient in the seated (A and B) or supine position (C). Seated-adjusted ABI
measurements (B) were calculated using corrected ABI formula.18 Created with Biorender. SBP, systolic blood
pressure.
JVS-Vascular Insights
Balaparya et al
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the unhoused population for PAD using seated-adjusted
and supine ABI in a mobile vascular laboratory.
Table I. Ankle-brachial index (ABI) interpretation: ABI
measurement range with corresponding peripheral arterial disease (PAD) diagnosis20
METHODS
ABI measurement
Data collection. Our study did not require institutional
review board approved protocol because no research
intervention was performed. Most of our participants
were native English speakers. We had native Spanishspeaking volunteers at each event, and we encountered one Mandarin speaking-only participant who
required a volunteer Mandarin interpreter. Patient information was collected using a paper medical intake form.
Prospective data from patients experiencing housing
and financial instabilities were collected at five independent MMCs from 2020 to 2022. MMCs were conducted in
partnership with local organizations that have established services to the unhoused and housing insecure
communities. PAD screening and other health care services were provided to all patients encountered at
MMCs as previously described by Boelitz et al.13
<0.50
Severe PAD
0.79-0.50
Moderate PAD
ABI measurement. PAD screening with ABI was performed by certified vascular laboratory technologists using appropriately sized blood pressure cuffs and a
portable continuous-wave 8-MHz Doppler transducer
(Fig 1). The ABI was calculated by dividing the highest
ankle systolic blood pressure at which Doppler signal
returned after blood pressure cuff compression by the
highest brachial systolic blood pressure at which Doppler
signal returned after blood pressure cuff compression of
a resting patient.22
Seated brachial and ankle systolic blood pressure measurements were performed with the patient seated in a
standard folding chair with the arm rested on a table
at the level of the chest. Seated-adjusted ABI was performed in a similar manner as outlined for seated ABI
with the addition of measuring the distance between
the brachial artery and posterior tibial artery with the patient in the seated position (Fig 1). A correction factor accounting for the distance between the brachial artery
and posterior tibial artery with the patient in the seated
position and the specific gravity of blood and mercury
(0.78).18 The formula is as follows:
Corrected ABI ¼
Measured ankle pressure D 0:078
Measured brachial pressure
Supine ABI brachial and ankle systolic blood pressure
measurements were performed with the patient lying
on a standard massage folding table with a maximum
weight capacity of 450 lbs. Patients found to have
noncompressible ABIs from all three ABI methods were
referred to our institution’s vascular laboratory for toebrachial index (TBI) testing, consistent with our institution’s practice for noncompressible ABI.
ABI feasibility assessment. The feasibility of incorporating seated, seated-adjusted, and supine ABI at MMCs
Interpretation
0.89-0.80
Mild PAD
0.90-1.29
Normal
$1.30
Indeterminant (noncompressible)
was determined by comparing equipment cost and the
number of patients screened with each ABI measurement method.
Statistical analysis. ABI measurements were considered either normal (ABI <1.3 and $ 0.9), mild to moderate PAD (ABI <0.9 and $ 0.5), severe PAD (ABI <0.5), or
noncompressible (ABI $ 1.3) (Table I). Statistical differences between seated, seated-adjusted, and supine ABI
were performed with two-way analysis of variance and/or
Student t test. Statistical significance was determined at
the P # .05 level. Analyses were conducted in SPSS 29
(SPSS Inc, Chicago, IL) and Prism 10.2.3 (GraphPad Software, Boston, MA).
RESULTS
Study cohort. Five MMCs focused on patients experiencing homelessness or housing insecurities were conducted in Central Massachusetts from 2020 and 2022.
MMCs were attended by a total of 166 patients; 89
(36%) were evaluated for PAD with ABI testing. An
average of 33 patients were evaluated at each MMC
over a 4-hour period. Participating patients were primarily men, with an average age of 56 years.
ABI measurement methodology. All patients were
offered ABI screening; however, the range of ABI testing
completed at each MMC varied greatly, between 21%
and 97% among MMC events 1 to 5 (Table II). Owing to
limited resources, seated ABI was only performed at
MMCs 1 and 2. At later MMC events, seated, seatedadjusted, and supine ABIs were performed. A total of
the 89 patients underwent PAD screening with one or
more ABI measurement method at five MMC events
(Table II).
Seated ABI examinations were performed on 88 patients (99% of total ABIs) (Table II). The seated ABI measurements at all MMC events ranged from 0.67 to 1.86
with an average of 1.34. Not surprisingly, 67% of patients
(59/88) were identified with noncompressible ABIs. Two
patients were found to screen positive for PAD, with an
ABI of 0.67 and 0.80, with the seated ABI. The remaining
27 patients were found to have normal ABIs.
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Table II. Number of patient participants with ankle-brachial index (ABI) measurements at multidisciplinary mobile clinic
(MMC) events
MMC Date
Total MMC patients screened
Participants measured Female
with any method
sex
Mean age participants, years
Seated ABI
measured
Seated-adjusted
ABI measured
Supine ABI
measured
48.7 6 15.0
11
n/a
n/a
November
2020
52
11 (21)
23 (44)
June 2021
30
29 (97)
10 (33)
54.1 6 11.9
29
n/a
n/a
November
2021
23
14 (61)
11 (48)
60.6 6 12.1
14
14
13
May 2022
38
19 (49)
6 (16)
67.3 6 13.9
18
16
15
November
2022
23
17 (74)
7 (30)
48.9 6 13.8
17
12
15
166
90 (54)
57 (34)
55.7 6 15.5
88
42
43
Total
Values are number (%) or mean 6 standard deviation.
Seated-adjusted ABI examinations were performed on
42 patients (47% of total ABIs) (Table II). The seatedadjusted ABI measurements at all MMC events ranged
from 0.59 to 1.75, with an average of 1.29. Noncompressible ABIs were identified in 38% of patients (16/42). Three
patients were found to screen positive for PAD, with an
ABI of 0.59, 0.80, and 0.87, respectively, with the seated
ABI. The remaining 16 patients were found to have
normal ABIs.
Supine ABI examinations were performed on 43 patients (48% of total ABIs) (Table II) and ranged from
0.70 to 1.95 with an average of 1.14. Noncompressible
ABIs were identified in 16% of patients (7/43). Three patients were found to screen positive for PAD, with an
ABI of 0.70, 0.79, and 0.87, when measured using supine
ABI. The majority, 36 patients, were found to have normal
ABIs.
Comparison between seated ABI, seated-adjusted,
and supine ABI. We were surprised to observe the high
percentage of noncompressible ABIs measured using
seated-adjusted ABIs when compared with supine ABIs
(38% vs 16%) (Fig 2). To test the accuracy of seated and
seated-adjusted ABIs when compared supine ABIs, 38
patients had all three screenings ABI methods performed (43% of screened patients).
The average seated ABI significantly differed from supine ABI (1.34 vs 1.14; P < .0001) (Fig 2). The average seated
ABI also significantly differed from seated-adjusted ABI
(1.34 vs 1.29; P ¼ .026) (Fig 2). The average seatedadjusted ABI significantly differed from supine ABI (1.28
vs 1.14; P ¼ .0204) (Fig 2). PAD screening at MMC events
yielded a high rate of noncompressible ABIs, in particular
when measurements were done with seated ABI (59/89
[66%]) (Figs 3 and 4). Two patients were found to have
mild to moderate PAD based on seated ABI. Twentyseven patients were found to have normal peripheral artery perfusion based on seated ABI (27/89 [30%]). To
determine whether the noncompressible patient population screened at MMCs had true calcific vessel arterial
disease or was falsely elevated owing to seated position,
we compared ABI measurements in the seated, seatedadjusted, and supine positions for patients attending
MMC events 3 through 5. Seated ABI demonstrated
noncompressible PAD in 32 patients (32/38 [84%])
screened. Of the 32 noncompressible seated-ABI,
Fig 2. Mean ankle-brachial index (ABI) measured using
three different methods at each multidisciplinary mobile
clinic (MMC) event. Noncompressible ABI denotated at
$1.3.
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false-positive ABI with low positive predictive value for
identifying noncompressible vessels using seated and
seated-adjusted ABI, which implies that these methods
are not accurate for PAD screening.
Fig 3. Distribution of seated ankle-brachial index (ABI) at
each multidisciplinary mobile clinic (MMC) event.
Noncompressible seated ABI denotated at $1.3.
seated-adjusted ABI agreed and was persistently
noncompressible in 24 patients (24/38 [63%]). Among patients found to have noncompressible ABI with either
seated or seated-adjusted ABI, supine ABI confirmed
noncompressible PAD in only four patients and an additional two patients who had tested compressible previously (6/38 [16%]). When compared with the gold
standard supine ABI, seated ABI is 83% sensitive for identifying noncompressible PAD, 16% specific, with a 14%
positive predictive value and an 86% negative predictive
value at accurately identifying noncompressible vessels.
Seated-adjusted ABI is 67% sensitive for identifying
noncompressible PAD, 38% specific, with a 17% positive
predictive value, and 86% negative predictive value at
correctly identifying noncompressible vessels (Table III).
These data suggest that there is a high number of
Feasibility of PAD screening at MMCs. At the first two
MMC events, only seated ABIs were performed given
the limited MMC budget and infrastructure to perform
supine ABIs. Blood pressure cuffs, handheld Doppler machines, and ultrasound gel were donated graciously to
MMC events through our academic institution. Seated
and seated-adjusted ABI measurements required a
folding chair, measuring tape, and table, which were
often provided by each hosting organization event free of
cost or was purchased for $80. The cost of a stretcher was
estimated to be $3000 and weighed 75 lbs. Cost, storage
size limitations, and heavy weight made it not logistically
feasible for our nonprofit MMC group to perform supine
ABI using medical stretchers. At MMC events 3 through 5,
supine ABI was performed using a foldable massage
table. After obtaining grant funding, MMC purchased
foldable massage tables for approximately $150 that
weighed 33 lbs. and could support patients #450 lbs. The
cost of a foldable massage table is 5% of the cost of a
medical stretcher, making the option for supine ABI
measurements financially feasible.
To test the technical feasibility of performing supine
ABI measurements using the massage folding table,
the number of patients screened for PAD using any ABI
method was compared with the number of supine ABI
performed at MMC events 3 through 5. A total of 49 patients had any ABI measurements recorded at MMC
events 3 through 5. Of the 49 patients with any ABI measurements, 43 received supine ABIs using the massage
Fig 4. Number of compressible and noncompressible ankle-brachial index (ABI) results by ABI measurement
methods performed on the same patient cohort. Thirty-eight patients underwent seated, seated-adjusted, and
supine ABI measurements. Bars represent the number of compressible ABIs (blue) and noncompressible ABIs
(maroon) using the indicated ABI measurement method. Compressive ABI <1.3 and noncompressible ABI $1.3.
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Table III. Sensitivity, specificity, positive and negative predictive values for seated-adjusted and seated ankle-brachial index
(ABI)
Result
Noncompressible
Compressible
Total
Noncompressible
4
20
24
PPV: 17%
Compressible
2
12
14
NPV: 86%
Total
6
32
Seated-adjusted ABI
Sensitivity: 67%
Specificity: 38%
Seated ABI
Noncompressible
5
27
32
PPV: 16%
Compressible
1
5
6
NPV: 83%
Total
6
32
Sensitivity: 83%
Specificity: 16%
NPV, Negative predictive value; PPV, positive predictive value.
Reported values are in reference to gold standard supine ABI. Compressible ABI is <1.3 and noncompressible ABI is $1.3.
folding table (43/49 [88%]) (Table II). These data demonstrate that performing supine ABI in a mobile outreach
setting is technically feasible.
DISCUSSION
Rising health care costs and socioeconomically disadvantaged communities contribute to significant disparities in PAD screening.3e5 To address this issue, several
groups have implemented mobile clinics to provide
accessible PAD screening to underserved populations.9,10,13 As mobile PAD screening clinics expand, it is
crucial to understand the unique challenges of screening
PAD with ABI measurements in outreach settings. Our
study explored the feasibility of introducing vascular
screening in an MMC and evaluated different methods
of ABI measurement within the resource constraints of
this setting. We found that seated and seated-adjusted
ABI measurements are unreliable and that, to accurately
diagnose PAD, ABIs must be obtained in the supine
position.
Although supine ABI measurements can be performed
easily in a clinic setting, this is not the case in a mobile
outreach setting. The medical stretcher required for supine ABI cost approximately $3000 and poses logistic
challenges regarding stretcher transportation and longterm storage between MMCs. Furthermore, only 54% of
patient participants at MMCs (89/166) agreed to proceed
with ABI testing when offered owing to the cumbersome
need to remove shoes and socks in a public setting.
Owing to these challenges, we evaluated seated ABI
testing for PAD screening MMC 1 and MMC 2.
Performing seated ABI measurements is appealing at
MMCs because it provides fast patient screening turnover. This is evident by the 97% (29/30) of participants
receiving seated only ABIs at MMC 2 event over a 4hour period in comparison with ABI testing rates
observed at later MMC events when seated-adjusted
and supine ABIs were incorporated (an average
screening rate of 61% [49/84]) (Table II). However, despite
the faster patient screening turnover with seated ABI,
this method resulted in a significantly higher rate of
falsely positive noncompressible ABI measurements.
The high number of patients who had noncompressible
seated ABI could be due to increased hydrostatic ankle
pressure from patients being in a seated position
(Fig 4). To address the issue of falsely elevated seated
ABI owing to gravitational effects and to avoid the
need for a medical stretcher required for supine ABI
measurements, seated-adjusted ABI has been reported
to provide accurate ABI measurements for PAD
screening.18 Gornik et al18 describe a strong correlation
between supine ABI and seated-adjusted ABI (using a
corrective factor to adjust for gravitational pressures in
the seated position) when performed in a clinical
vascular lab setting. In our study, we did not observe a
correlation between supine and seated-adjusted ABI,
but instead observed a high rate of falsely elevated
ABIs obtained using the seated-adjusted calculation.
There are important differences between our study
design and Gornik et al that may explain these differences. Seated and seated-adjusted ABI measurements
in our study were done at MMCs conducted primarily
outdoors, which may present difficulties to accurately
auscultate changes in Doppler in comparison with a
quieter vascular laboratory setting. In Gornik et al,
seated-adjusted ABIs were calculated after the supine
ABIs were obtained, which may shorten the time of gravity effect on seated ABI measurements. In contrast, in our
study, seated ABI measurements were collected before
placing the patient in the supine position, thus prolonging the effect of gravity. These differences in study design
may account for the discordant correlation between supine ABI and seated-adjusted ABI reported in our study.
Based on our experience, supine and supine-adjusted
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ABI measurements in a MMC setting yielded a high rate
of falsely elevated noncompressible ABIs, thus making
these ABI methods less accurate for PAD screening at
mobile outreach clinics when compared with supine
ABI.
Based on the superiority of supine ABI for PAD
screening at MMCs identified in our study, we have
now transitioned to only performing supine ABIs at all
MMC events. The technical and logistical challenges of
performing supine ABIs at MMCs have been addressed
with the use of economical, foldable massage tables
with a weight capacity of #450 lbs. The cost of a foldable
massage table is 5% of the cost of a medical stretcher,
making the option for supine ABI measurements logistically feasible.
Finally, it is important to note that establishing ABI
testing and encouraging patient participation at MMC
required a learning curve as evident by only 21% of total
patient participants being screened at MMC 1(11/52) and
later an increase of 97% (29/30) ABI testing done at
MMC event 2. Patient participation in ABI measurements
were encouraged by offering foot washes and podiatry
foot examinations immediately before or after ABI
testing to limit the number of times patients were asked
to remove their socks and shoes. In addition, patient participants who completed ABI testing were incentivized
with donated new sneakers and socks. Designing innovative ways in which to promote ABI measurement participation is key to the success of any program intending to
screen for PAD.
our city. Although clinics were promoted by organizations already connected with the unhoused population
and promoted the events weeks in advance, we are
aware that individuals who attended were able to transport themselves to the event on foot, were connected
directly or indirectly with the organizations advertising
the MMCs, and trusted the medical providers enough
to participate; this combination of factors could have
excluded individuals with limited mobility, without access to local resources, and those who have a mistrust
of the health care system. Given these limitations, we
have not used these data as representative of the burden
of vascular disease among the unhoused population in
Worcester, Massachusetts; our focus is on feasibility of
screening and identifying the best screening method in
the MMC setting.
CONCLUSIONS
Our findings underscore the feasibility of using ABI
screening in mobile clinic settings and the importance
of using supine position measurements vs alternative positions. Vascular health for individuals experiencing
homelessness and housing insecurity may be improved
through mobile clinics but requires addressing environmental challenges and optimizing protocols to ensure
accurate diagnosis and equitable health care delivery.
Future research should focus on strategies to enhance
ABI testing effectiveness in resource-limited environments and improve PAD screening in vulnerable
communities.
LIMITATIONS
AUTHOR CONTRIBUTIONS
The MMC environment is inherently variable and unpredictable regarding weather and temperature. Even with
an experienced technologist and suitable portable
equipment, the variable temperature and noise or patient distractions in a mobile clinic are different from a
controlled vascular laboratory. We can compare the results of different ABI measurement methods performed
at each MMC to each other but cannot presume that supine ABI measured at an MMC is equivalent to supine
ABI measured in a vascular laboratory.
In our institution’s vascular laboratory, it is also standard
practice to conduct TBI on patients with diabetes and
with noncompressible ankle measurements. Unfortunately, this equipment was not feasible to use in the
MMC setting owing to cost and ambient temperature requirements for TBI measurements. MMC events are often
held outdoors and, therefore, ambient temperature is
less controlled than in a vascular laboratory. Changes in
ambient temperature can impact vasoconstriction and/
or vasodilation that will impact the accuracy of TBI
measurements.
We also acknowledge that participants in MMCs may
not be representative of the unhoused population in
DISCLOSURES
Conception and design: SB, TN
Analysis and interpretation: SB, RC, JS, DJ, AS, TN
Data collection: SB, JL, TN
Writing the article: SB, RC, TN
Critical revision of the article: SB, RC, JL, JS, DJ, AS, TN
Final approval of the article: SB, RC, JL, JS, DJ, AS, TN
Statistical analysis: SB, RC, TN
Obtained funding: TN
Overall responsibility: TN
SB and RG contributed equally to this article and share
co-first authorship.
None.
REFERENCES
1. Hess CN, Hicks CW, Kwan TW, McDermott MM. Lower extremity
peripheral artery disease: contemporary epidemiology, management gaps, and future directions: a scientific statement from the
American Heart Association. Circulation. 2021;144:e171ee191.
2. Nordanstig J, Behrendt CA, Bradbury AW, et al. Peripheral arterial
disease (PAD) - a challenging manifestation of atherosclerosis. Prev
Med. 2023;171:107489.
3. Barnes JA, Eid MA, Creager MA, Goodney PP. Epidemiology and risk
of amputation in patients with diabetes Mellitus and peripheral artery disease. Arterioscler Thromb Vasc Biol. 2020;40:1808e1817.
8
JVS-Vascular Insights
Balaparya et al
2024
4. Barshes NR, Minc SD. Healthcare disparities in vascular surgery: a
critical review. J Vasc Surg. 2021;74:6Se14S.e1.
5. McDermott KM, Bose S, Keegan A, Hicks CW. Disparities in limb
preservation and associated socioeconomic burden among patients
with diabetes and/or peripheral artery disease in the United States.
Semin Vasc Surg. 2023;36:39e48.
6. Soden PA, Zettervall SL, Deery SE, et al. Black patients present with
more severe vascular disease and a greater burden of risk factors
than white patients at time of major vascular intervention. J Vasc
Surg. 2018;67:549e556.e3.
7. Coaston A, Lee SJ, Johnson J, Hardy-Peterson M, Weiss S, Stephens C.
Mobile medical clinics in the United States Post-Affordable care Act:
an Integrative review. Popul Health Manag. 2022;25:264e279.
8. Yu SW, Hill C, Ricks ML, Bennet J, Oriol NE. The scope and impact of
mobile health clinics in the United States: a literature review. Int J
Equity Health. 2017;16:178.
9. Solaru KTW, Coy T, SeLozier S, et al. Findings of a novel barbershopbased peripheral artery disease screening program for Black men.
J Am Heart Assoc. 2022;11:e026347.
10. Minc SD, Powell C, Drudi LM, et al. Community-engaged research in
vascular surgery: an approach to decrease amputation disparities
and effect population-level change. Semin Vasc Surg. 2023;36:
100e113.
11. Al-Shakarchi NJ, Evans H, Luchenski SA, Story A, Banerjee A. Cardiovascular disease in homeless versus housed individuals: a systematic review of observational and interventional studies. Heart.
2020;106:1483e1488.
12. Gao J, Qu H, McGregor KM, Yadav AS, Yuen HK. Associations between duration of homelessness and cardiovascular risk factors: a
pilot study. Int J Environ Res Publ Health . 2022;19:14698.
13. Boelitz KM, Lee J, Cayton C, et al. Utilizing mobile diabetic foot clinics
to provide comprehensive care to patients experiencing homelessness. Ann Vasc Surg. 2023;89:97e98.
14. McDermott KM, Srinivas T, Abularrage CJ. Multidisciplinary approach
to decreasing major amputation, improving outcomes, and
15.
16.
17.
18.
19.
20.
21.
22.
mitigating disparities in diabetic foot and vascular disease. Semin
Vasc Surg. 2023;36:114e121.
Hingorani A, LaMuragila GM, Henke P, et al. The management of
diabetic foot: a clinical practice guideline by the Society for Vascular
Surgery in collaboration with the American Podiatric Medical Association and the Society for Vascular Medicine. J Vasc Surg. 2016;63(2
Suppl):3Se21S.
Herraiz-Adillo A, Cavero-Redondo I, Alvarez-Bueno C, PozueloCarrascosa DP, Solera-Martinez M. The accuracy of toe brachial index
and ankle brachial index in the diagnosis of lower limb peripheral
arterial disease: a systematic review and meta-analysis. Atherosclerosis. 2020;315:81e92.
Ko SH, Bandyk DF. Interpretation and significance of ankle-brachial
systolic pressure index. Semin Vasc Surg. 2013;26:86e94.
Gornik HL, Garcia B, Wolski K, Jones DC, Macdonald KA. Validation of
a method for determination of the ankle-brachial index in the
seated position. J Vasc Surg. 2008;48:1204e1210.
Paskiewicz A, Wang FM, Yang C, et al. Ankle-brachial index and
subsequent risk of severe ischemic leg outcomes: the ARIC study.
J Am Heart Assoc. 2021;10:e021801.
Guirguis-Blake JM, Evans CV, Redmond N, Lin JS. Screening for peripheral artery disease using the ankle-brachial index updated evidence report and systematic review for the US preventive services
task force. JAMA. 2018;320:184e196.
Singh GD, Armstrong EJ, Waldo SW, et al. Non-compressible ABIs are
associated with an increased risk of major amputation and major
adverse cardiovascular events in patients with critical limb ischemia.
Vasc Med. 2017;22:210e217.
Aboyans V, Criqui MH, Abraham P, et al. Measurement and interpretation of the ankle-brachial index: a scientific statement from the
American Heart association. Circulation. 2012;126:2890e2909.
Submitted Jun 5, 2024; accepted Jul 21, 2024.