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A Comparison of Programmable and Non-Programmable Compression Devices for Treatment of Lymphedema Using an Administrative Health Outcomes Dataset.

Identifieur interne : 000164 ( PubMed/Corpus ); précédent : 000163; suivant : 000165

A Comparison of Programmable and Non-Programmable Compression Devices for Treatment of Lymphedema Using an Administrative Health Outcomes Dataset.

Auteurs : P. Karaca-Mandic ; A T Hirsch ; S G Rockson ; S H Ridner

Source :

RBID : pubmed:28573790

Abstract

Patients with lymphedema suffer lifelong swelling and recurrent cellulitis despite use of complete decongestive therapy. Pneumatic compression devices (PCDs), including non-programmable and programmable devices that meet individual patient needs, support long term self-care in the home. Yet, to date, no direct comparison of their relative benefits has been available.

DOI: 10.1111/bjd.15699
PubMed: 28573790

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pubmed:28573790

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<name sortKey="Karaca Mandic, P" sort="Karaca Mandic, P" uniqKey="Karaca Mandic P" first="P" last="Karaca-Mandic">P. Karaca-Mandic</name>
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<nlm:affiliation>Division of Health Policy and Management, University of Minnesota School of Public Health, Minneapolis.</nlm:affiliation>
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<name sortKey="Hirsch, A T" sort="Hirsch, A T" uniqKey="Hirsch A" first="A T" last="Hirsch">A T Hirsch</name>
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<nlm:affiliation>Cardiovascular Division, University of Minnesota Medical School, Minneapolis.</nlm:affiliation>
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<name sortKey="Rockson, S G" sort="Rockson, S G" uniqKey="Rockson S" first="S G" last="Rockson">S G Rockson</name>
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<nlm:affiliation>Falk Cardiovascular Research Center, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
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<name sortKey="Ridner, S H" sort="Ridner, S H" uniqKey="Ridner S" first="S H" last="Ridner">S H Ridner</name>
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<nlm:affiliation>Vanderbilt University School of Nursing, Nashville, Tennessee (Ridner); Vanderbilt Ingram Cancer Center, Nashville, Tennessee.</nlm:affiliation>
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<name sortKey="Ridner, S H" sort="Ridner, S H" uniqKey="Ridner S" first="S H" last="Ridner">S H Ridner</name>
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<title level="j">The British journal of dermatology</title>
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<div type="abstract" xml:lang="en">Patients with lymphedema suffer lifelong swelling and recurrent cellulitis despite use of complete decongestive therapy. Pneumatic compression devices (PCDs), including non-programmable and programmable devices that meet individual patient needs, support long term self-care in the home. Yet, to date, no direct comparison of their relative benefits has been available.</div>
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<ArticleTitle>A Comparison of Programmable and Non-Programmable Compression Devices for Treatment of Lymphedema Using an Administrative Health Outcomes Dataset.</ArticleTitle>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/bjd.15699</ELocationID>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Patients with lymphedema suffer lifelong swelling and recurrent cellulitis despite use of complete decongestive therapy. Pneumatic compression devices (PCDs), including non-programmable and programmable devices that meet individual patient needs, support long term self-care in the home. Yet, to date, no direct comparison of their relative benefits has been available.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">Patients who acquired either a non-programmable device (NP-PCD) or a dynamic pressure programmable device (P-PCD; Flexitouch(®) ) were evaluated to compare associated clinical and health utilization outcomes pre/post-device acquisition.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Retrospective analysis of de-identified administrative claims from 2007 through 2013 of a large United States insurer. The study populations were defined pre hoc as distinct cancer- and non-cancer-related lymphedema cohorts. Outcome variables included rates of lymphedema-related cellulitis, manual therapy use, outpatient services, and inpatient hospitalizations. Multivariate regression analysis was performed to: (1) compare outcomes for the 12 months pre- and post-device acquisition and (2) compare these two device types for their treatment-associated benefits.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The sample consisted of 1,013 NP-PCD and 718 P-PCD recipients. Compared with the NP-PCD group, P-PCD patients' baseline cellulitis rate was higher, while their post-device cellulitis rate was lower. In the cancer cohort, the NP-PCD group had a 53% reduction in episodes of cellulitis (from 17.9% to 8.5%), compared to a greater 79% reduction in the P-PCD group (from 23.7% to 5.0%) (p<0.001). In the non-cancer cohort, the P-PCD group also experienced a larger 76% decline (from 31.7% to 7.4%) vs. 54% decline (from 22.9% to 10.6%) in cellulitis rates (p=0.003). Outpatient service use reduced in both device groups, with greater reductions observed in P-PCD group. Both device groups experienced reductions in manual therapy use. Inpatient hospitalizations were largely stable with reductions observed only in the non-cancer cohort of the P-PCD group.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">P-PCD receipt was associated with superior lymphedema-related health outcomes and reductions in cellulitis. This article is protected by copyright. All rights reserved.</AbstractText>
<CopyrightInformation>This article is protected by copyright. All rights reserved.</CopyrightInformation>
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