Observational study of the acceptability of Sayana® Press among intramuscular DMPA users in Uganda and Senegal

Abstract Background Sayana® Press (SP), a subcutaneous formulation of depot medroxyprogesterone acetate (DMPA) in Uniject™, has potential to be a valuable innovation in family planning (FP) because it may overcome logistic and safety challenges in delivering intramuscular DMPA (DMPA IM). However, SP...

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Veröffentlicht in:Contraception (Stoneham) 2014-05, Vol.89 (5), p.361-367
Hauptverfasser: Burke, Holly M, Mueller, Monique P, Perry, Brian, Packer, Catherine, Bufumbo, Leonard, Mbengue, Daouda, Mall, Ibrahima, Daff, Bocar Mamadou, Mbonye, Anthony K
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container_end_page 367
container_issue 5
container_start_page 361
container_title Contraception (Stoneham)
container_volume 89
creator Burke, Holly M
Mueller, Monique P
Perry, Brian
Packer, Catherine
Bufumbo, Leonard
Mbengue, Daouda
Mall, Ibrahima
Daff, Bocar Mamadou
Mbonye, Anthony K
description Abstract Background Sayana® Press (SP), a subcutaneous formulation of depot medroxyprogesterone acetate (DMPA) in Uniject™, has potential to be a valuable innovation in family planning (FP) because it may overcome logistic and safety challenges in delivering intramuscular DMPA (DMPA IM). However, SP's acceptability is unknown. We measured acceptability of SP among DMPA IM users. Study design This open-label observational study was conducted in clinics in three districts in Senegal and community-based distribution services in two districts in Uganda. Experienced DMPA IM users were offered SP by community health workers (CHWs) or clinic-based providers. SP decliners were asked to discuss their reasons. Those who received SP were interviewed pre- and postinjection and 3 months later, when they were asked if they would select SP over DMPA IM if it were available. Results One hundred twenty women in Uganda and 242 in Senegal received SP (117 and 240 were followed up, respectively). Nine Ugandan and seven Senegalese SP decliners were interviewed. Three months after receiving SP, 84% [95% confidence interval (CI)=75%–93%] of Ugandan participants and 80% (95% CI=74%–87%) of Senegalese participants said they would select SP over DMPA IM. Main reasons for selecting SP were fewer side effects, liking the method, fast administration, less pain and method effectiveness. Thirty-four adverse events were reported but were not serious. No pregnancies were reported. Conclusion Current DMPA IM users in Senegal and Uganda accepted SP, and most preferred SP over DMPA IM. SP can be safely introduced into FP programs and administered by trained CHWs, with expectation of client uptake. Implications We found SP acceptable and safe in diverse settings among current intramuscular DMPA users, including those who received SP from CHWs. This provides evidence that SP would be used and could therefore reduce unmet family planning needs if introduced into family planning programs.
doi_str_mv 10.1016/j.contraception.2014.01.022
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However, SP's acceptability is unknown. We measured acceptability of SP among DMPA IM users. Study design This open-label observational study was conducted in clinics in three districts in Senegal and community-based distribution services in two districts in Uganda. Experienced DMPA IM users were offered SP by community health workers (CHWs) or clinic-based providers. SP decliners were asked to discuss their reasons. Those who received SP were interviewed pre- and postinjection and 3 months later, when they were asked if they would select SP over DMPA IM if it were available. Results One hundred twenty women in Uganda and 242 in Senegal received SP (117 and 240 were followed up, respectively). Nine Ugandan and seven Senegalese SP decliners were interviewed. Three months after receiving SP, 84% [95% confidence interval (CI)=75%–93%] of Ugandan participants and 80% (95% CI=74%–87%) of Senegalese participants said they would select SP over DMPA IM. Main reasons for selecting SP were fewer side effects, liking the method, fast administration, less pain and method effectiveness. Thirty-four adverse events were reported but were not serious. No pregnancies were reported. Conclusion Current DMPA IM users in Senegal and Uganda accepted SP, and most preferred SP over DMPA IM. SP can be safely introduced into FP programs and administered by trained CHWs, with expectation of client uptake. Implications We found SP acceptable and safe in diverse settings among current intramuscular DMPA users, including those who received SP from CHWs. This provides evidence that SP would be used and could therefore reduce unmet family planning needs if introduced into family planning programs.</description><identifier>ISSN: 0010-7824</identifier><identifier>EISSN: 1879-0518</identifier><identifier>DOI: 10.1016/j.contraception.2014.01.022</identifier><identifier>PMID: 24631328</identifier><identifier>CODEN: CCPTAY</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Biological and medical sciences ; Community health worker ; Contraception ; Contraceptive Agents, Female - administration &amp; dosage ; Depot medroxyprogesterone acetate ; Female ; Genital system. Reproduction ; Gynecology. Andrology. Obstetrics ; Humans ; Injections, Subcutaneous ; Medical sciences ; Medroxyprogesterone Acetate - administration &amp; dosage ; Obstetrics and Gynecology ; Patient Acceptance of Health Care - statistics &amp; numerical data ; Pharmacology. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-7aa14ca04efff224e89ad3f0e01d12561eda0c5ebce73335b74a414a50a406123</citedby><cites>FETCH-LOGICAL-c468t-7aa14ca04efff224e89ad3f0e01d12561eda0c5ebce73335b74a414a50a406123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.contraception.2014.01.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28535450$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24631328$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burke, Holly M</creatorcontrib><creatorcontrib>Mueller, Monique P</creatorcontrib><creatorcontrib>Perry, Brian</creatorcontrib><creatorcontrib>Packer, Catherine</creatorcontrib><creatorcontrib>Bufumbo, Leonard</creatorcontrib><creatorcontrib>Mbengue, Daouda</creatorcontrib><creatorcontrib>Mall, Ibrahima</creatorcontrib><creatorcontrib>Daff, Bocar Mamadou</creatorcontrib><creatorcontrib>Mbonye, Anthony K</creatorcontrib><title>Observational study of the acceptability of Sayana® Press among intramuscular DMPA users in Uganda and Senegal</title><title>Contraception (Stoneham)</title><addtitle>Contraception</addtitle><description>Abstract Background Sayana® Press (SP), a subcutaneous formulation of depot medroxyprogesterone acetate (DMPA) in Uniject™, has potential to be a valuable innovation in family planning (FP) because it may overcome logistic and safety challenges in delivering intramuscular DMPA (DMPA IM). However, SP's acceptability is unknown. We measured acceptability of SP among DMPA IM users. Study design This open-label observational study was conducted in clinics in three districts in Senegal and community-based distribution services in two districts in Uganda. Experienced DMPA IM users were offered SP by community health workers (CHWs) or clinic-based providers. SP decliners were asked to discuss their reasons. Those who received SP were interviewed pre- and postinjection and 3 months later, when they were asked if they would select SP over DMPA IM if it were available. Results One hundred twenty women in Uganda and 242 in Senegal received SP (117 and 240 were followed up, respectively). Nine Ugandan and seven Senegalese SP decliners were interviewed. Three months after receiving SP, 84% [95% confidence interval (CI)=75%–93%] of Ugandan participants and 80% (95% CI=74%–87%) of Senegalese participants said they would select SP over DMPA IM. Main reasons for selecting SP were fewer side effects, liking the method, fast administration, less pain and method effectiveness. Thirty-four adverse events were reported but were not serious. No pregnancies were reported. Conclusion Current DMPA IM users in Senegal and Uganda accepted SP, and most preferred SP over DMPA IM. SP can be safely introduced into FP programs and administered by trained CHWs, with expectation of client uptake. Implications We found SP acceptable and safe in diverse settings among current intramuscular DMPA users, including those who received SP from CHWs. This provides evidence that SP would be used and could therefore reduce unmet family planning needs if introduced into family planning programs.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Community health worker</subject><subject>Contraception</subject><subject>Contraceptive Agents, Female - administration &amp; dosage</subject><subject>Depot medroxyprogesterone acetate</subject><subject>Female</subject><subject>Genital system. Reproduction</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Injections, Subcutaneous</subject><subject>Medical sciences</subject><subject>Medroxyprogesterone Acetate - administration &amp; dosage</subject><subject>Obstetrics and Gynecology</subject><subject>Patient Acceptance of Health Care - statistics &amp; numerical data</subject><subject>Pharmacology. 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Reproduction</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Injections, Subcutaneous</topic><topic>Medical sciences</topic><topic>Medroxyprogesterone Acetate - administration &amp; dosage</topic><topic>Obstetrics and Gynecology</topic><topic>Patient Acceptance of Health Care - statistics &amp; numerical data</topic><topic>Pharmacology. 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However, SP's acceptability is unknown. We measured acceptability of SP among DMPA IM users. Study design This open-label observational study was conducted in clinics in three districts in Senegal and community-based distribution services in two districts in Uganda. Experienced DMPA IM users were offered SP by community health workers (CHWs) or clinic-based providers. SP decliners were asked to discuss their reasons. Those who received SP were interviewed pre- and postinjection and 3 months later, when they were asked if they would select SP over DMPA IM if it were available. Results One hundred twenty women in Uganda and 242 in Senegal received SP (117 and 240 were followed up, respectively). Nine Ugandan and seven Senegalese SP decliners were interviewed. Three months after receiving SP, 84% [95% confidence interval (CI)=75%–93%] of Ugandan participants and 80% (95% CI=74%–87%) of Senegalese participants said they would select SP over DMPA IM. Main reasons for selecting SP were fewer side effects, liking the method, fast administration, less pain and method effectiveness. Thirty-four adverse events were reported but were not serious. No pregnancies were reported. Conclusion Current DMPA IM users in Senegal and Uganda accepted SP, and most preferred SP over DMPA IM. SP can be safely introduced into FP programs and administered by trained CHWs, with expectation of client uptake. Implications We found SP acceptable and safe in diverse settings among current intramuscular DMPA users, including those who received SP from CHWs. This provides evidence that SP would be used and could therefore reduce unmet family planning needs if introduced into family planning programs.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>24631328</pmid><doi>10.1016/j.contraception.2014.01.022</doi><tpages>7</tpages></addata></record>
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subjects Adult
Biological and medical sciences
Community health worker
Contraception
Contraceptive Agents, Female - administration & dosage
Depot medroxyprogesterone acetate
Female
Genital system. Reproduction
Gynecology. Andrology. Obstetrics
Humans
Injections, Subcutaneous
Medical sciences
Medroxyprogesterone Acetate - administration & dosage
Obstetrics and Gynecology
Patient Acceptance of Health Care - statistics & numerical data
Pharmacology. Drug treatments
Senegal
Subcutaneous injection
Uganda
Young Adult
title Observational study of the acceptability of Sayana® Press among intramuscular DMPA users in Uganda and Senegal
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