首页 > 最新文献

Gates Open Research最新文献

英文 中文
How resilient were family planning programs during the COVID-19 pandemic?  Evidence from 70 countries. 在 COVID-19 大流行期间,计划生育计划的复原力如何? 来自 70 个国家的证据。
Pub Date : 2024-03-25 eCollection Date: 2023-01-01 DOI: 10.12688/gatesopenres.14856.2
Karen Hardee, Rebecca Rosenberg, John Ross, Imelda Zosa-Feranil

Background: At the beginning of the COVID-19 pandemic fears of severe disruptions to family planning (FP) and access to services abounded. This paper uses a unique data source, a special Supplement added to the 2021 round of the National Composite Index for Family Planning (NCIFP), to assess in depth the resilience of FP programs in the face of the COVID-19 pandemic across 70 countries spanning six regions.

Methods: The 2021 NCIFP included 961 key informants who were asked questions to assess interference in the countries' ability to achieve objectives, ability to maintain commitment to FP, and availability of information and services. Open ended responses added context.

Results: All programs were affected; the magnitude of effects varies by region and country. While the average resilience score, at 47 out of 100, implies middling levels of resilience, further analysis showed that despite interference in many components of programming, with some exceptions, the COVID-19 pandemic generally did not diminish government commitment to FP and programs remained resilient in providing access to services. Common themes mentioned by 178 respondents (18.5% of respondents) included: fear of infection; disruption of services / difficulty with lockdown and travel restrictions; staff / facilities diverted to COVID-19; access to reproductive health services and contraceptive methods affected; shifts in services / outreach; interference with logistics & supplies, training & supervision, and M&E; lack of attention to FP/sexual reproductive health; financing reduced or diverted; and effects on existing partnerships. A strong enabling environment for FP, which the NCIFP is designed to measure, was positively correlated with continued government commitment and access to contraceptive methods during COVID-19.

Conclusion: These findings are instructive for programming: it will face challenges and 'interference' when unanticipated shocks like COVID-19 occur, with strong FP programs best prepared to exhibit resilience.

背景:在COVID-19大流行之初,人们普遍担心计划生育(FP)和服务的获取会受到严重干扰。本文使用了一个独特的数据源--2021年国家计划生育综合指数(NCIFP)中添加的特别补编--来深入评估横跨六个地区的70个国家的FP项目在COVID-19大流行时的恢复力:方法:2021年全国计划生育信息通报计划包括961名关键信息提供者,向他们提出问题,以评估各国实现目标的能力、保持对计划生育承诺的能力以及信息和服务的可用性等方面受到的干扰。开放式回答增加了背景信息:结果:所有计划都受到了影响;影响程度因地区和国家而异。虽然平均复原力得分(满分 100 分)为 47 分,意味着复原力处于中等水平,但进一步的分析表明,尽管 COVID-19 大流行对计划编制的许多部分造成了干扰,但除个别情况外,总体上并未削弱政府对计划生育的承诺,而且各计划在提供服务方面仍然保持了复原力。178 个受访者(占受访者的 18.5%)提到的共同主题包括:对感染的恐惧;服务中断/封锁和旅行限制带来的困难;工作人员/设施被转用于 COVID-19;生殖健康服务和避孕方法的获取受到影响;服务/外联的转变;对后勤和供应、培训和监督以及 M&E 的干扰;对计划生育/性生殖健康缺乏关注;资金减少或被转用;以及对现有伙伴关系的影响。在 COVID-19 期间,一个强有力的有利于计划生育的环境(NCIFP 旨在衡量这一环境)与政府的持续承诺和避孕方法的可及性呈正相关:这些研究结果对计划编制工作具有启发意义:当发生类似COVID-19这样的意外冲击时,计划编制工作将面临挑战和 "干扰",而强大的FP计划最能展现其复原力。
{"title":"How resilient were family planning programs during the COVID-19 pandemic?  Evidence from 70 countries.","authors":"Karen Hardee, Rebecca Rosenberg, John Ross, Imelda Zosa-Feranil","doi":"10.12688/gatesopenres.14856.2","DOIUrl":"10.12688/gatesopenres.14856.2","url":null,"abstract":"<p><strong>Background: </strong>At the beginning of the COVID-19 pandemic fears of severe disruptions to family planning (FP) and access to services abounded. This paper uses a unique data source, a special Supplement added to the 2021 round of the National Composite Index for Family Planning (NCIFP), to assess in depth the resilience of FP programs in the face of the COVID-19 pandemic across 70 countries spanning six regions.</p><p><strong>Methods: </strong>The 2021 NCIFP included 961 key informants who were asked questions to assess interference in the countries' ability to achieve objectives, ability to maintain commitment to FP, and availability of information and services. Open ended responses added context.</p><p><strong>Results: </strong>All programs were affected; the magnitude of effects varies by region and country. While the average resilience score, at 47 out of 100, implies middling levels of resilience, further analysis showed that despite interference in many components of programming, with some exceptions, the COVID-19 pandemic generally did not diminish government commitment to FP and programs remained resilient in providing access to services. Common themes mentioned by 178 respondents (18.5% of respondents) included: fear of infection; disruption of services / difficulty with lockdown and travel restrictions; staff / facilities diverted to COVID-19; access to reproductive health services and contraceptive methods affected; shifts in services / outreach; interference with logistics & supplies, training & supervision, and M&E; lack of attention to FP/sexual reproductive health; financing reduced or diverted; and effects on existing partnerships. A strong enabling environment for FP, which the NCIFP is designed to measure, was positively correlated with continued government commitment and access to contraceptive methods during COVID-19.</p><p><strong>Conclusion: </strong>These findings are instructive for programming: it will face challenges and 'interference' when unanticipated shocks like COVID-19 occur, with strong FP programs best prepared to exhibit resilience.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"7 ","pages":"121"},"PeriodicalIF":0.0,"publicationDate":"2024-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11111842/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141087370","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Expanding options for HIV testing: A process evaluation of a community-led HIV self-testing intervention among men who have sex with men in Kenya. 扩大艾滋病毒检测的选择范围:对肯尼亚男男性行为者中由社区主导的 HIV 自我检测干预措施进行过程评估。
Pub Date : 2024-03-25 eCollection Date: 2023-01-01 DOI: 10.12688/gatesopenres.14819.2
Memory Melon, Bernadette Kombo, Mary Mugambi, Margaret Njiraini, Kennedy Olango, Manas Migot, Samuel Kuria, Martin Kyana, Peter Mwakazi, Japheth Kioko, Shem Kaosa, Maria Mensah, Matthew Thomann, Janet Musimbi, Helgar Musyoki, Parinita Bhattacharjee, Robert Lorway, Lisa Lazarus

Background: Men who have sex with men (MSM) in Kenya continue to face barriers to HIV testing, which leads to delays in HIV prevention and care. An HIV self-testing (HIVST) intervention was implemented in three Kenyan counties to increase coverage and frequency of HIV testing among MSM communities with high HIV prevalence. The evaluation study examined how HIVST can increase testing among MSM who are unaware of their status by increasing coverage, frequency, and early uptake of testing and support linkages to prevention and treatment. We share results from the process evaluation of the intervention implemented in partnership with MSM-led organizations.

Methods: For a 12-month period between August 2019 and July 2020, the project team conducted in-depth interviews with HIVST users, monthly meetings with programme implementation teams, and monthly monitoring data reviews. Polling booth surveys were also conducted with participants. The process evaluation explored the fidelity, feasibility, coverage, acceptability, quality, and effectiveness of the HIVST intervention.

Results: An average of 793 MSM received 1,041 HIVST kits on a monthly basis through different distribution channels. Of those who received HIVST kits, 67% were distributed to infrequent testers and non-testers. Testing frequency among users increased to 82% for those who had a recent test during the previous three months, compared to 58% of HIVST non-users. There was a high linkage to care and treatment services (84%) among those who tested reactive for HIV at endline. MSM shared preferring HIVST kits because of its convenience and privacy. During the COVID-19 pandemic, adaptations to the intervention were made to support ongoing HIV testing and linkages to services.

Conclusion: The introduction of HIVST in MSM-led HIV prevention programmes was feasible with high acceptability. The involvement of the MSM community in the design, implementation and evaluation of the intervention was a key factor to intervention success.

背景:肯尼亚的男男性行为者(MSM)在接受 HIV 检测时仍然面临障碍,这导致了 HIV 预防和护理工作的延误。在肯尼亚的三个县实施了一项艾滋病病毒自我检测(HIVST)干预措施,以提高艾滋病病毒感染率较高的男男性行为者社区的艾滋病病毒检测覆盖率和频率。这项评估研究探讨了 HIVST 如何通过提高检测覆盖率、频率和早期接受率来增加对不了解自身状况的男男性行为者的检测,并支持将其与预防和治疗联系起来。我们分享了与 MSM 领导的组织合作实施干预措施的过程评估结果:在 2019 年 8 月至 2020 年 7 月的 12 个月期间,项目团队对 HIVST 用户进行了深入访谈,每月与计划实施团队举行会议,并每月进行监测数据审查。还对参与者进行了投票站调查。过程评估探讨了艾滋病毒检测干预措施的忠实性、可行性、覆盖面、可接受性、质量和有效性:通过不同的分发渠道,平均每月有 793 名男男性行为者收到 1,041 套艾滋病毒检测包。在收到艾滋病毒检测包的人中,67%的人被分发给了不经常检测和不检测的人。在过去三个月中最近接受过检测的使用者中,检测频率增加到 82%,而未接受过艾滋病毒检测的使用者中,检测频率为 58%。在终点线艾滋病毒检测呈反应性的人群中,接受护理和治疗服务的比例较高(84%)。男男性行为者表示,他们更喜欢使用艾滋病毒检测包,因为它既方便又能保护隐私。在 COVID-19 大流行期间,对干预措施进行了调整,以支持持续的艾滋病毒检测和服务链接:结论:在男男性行为者主导的艾滋病预防计划中引入 HIVST 是可行的,接受度也很高。男男性行为者社区参与干预措施的设计、实施和评估是干预措施取得成功的关键因素。
{"title":"Expanding options for HIV testing: A process evaluation of a community-led HIV self-testing intervention among men who have sex with men in Kenya.","authors":"Memory Melon, Bernadette Kombo, Mary Mugambi, Margaret Njiraini, Kennedy Olango, Manas Migot, Samuel Kuria, Martin Kyana, Peter Mwakazi, Japheth Kioko, Shem Kaosa, Maria Mensah, Matthew Thomann, Janet Musimbi, Helgar Musyoki, Parinita Bhattacharjee, Robert Lorway, Lisa Lazarus","doi":"10.12688/gatesopenres.14819.2","DOIUrl":"10.12688/gatesopenres.14819.2","url":null,"abstract":"<p><strong>Background: </strong>Men who have sex with men (MSM) in Kenya continue to face barriers to HIV testing, which leads to delays in HIV prevention and care. An HIV self-testing (HIVST) intervention was implemented in three Kenyan counties to increase coverage and frequency of HIV testing among MSM communities with high HIV prevalence. The evaluation study examined how HIVST can increase testing among MSM who are unaware of their status by increasing coverage, frequency, and early uptake of testing and support linkages to prevention and treatment. We share results from the process evaluation of the intervention implemented in partnership with MSM-led organizations.</p><p><strong>Methods: </strong>For a 12-month period between August 2019 and July 2020, the project team conducted in-depth interviews with HIVST users, monthly meetings with programme implementation teams, and monthly monitoring data reviews. Polling booth surveys were also conducted with participants. The process evaluation explored the fidelity, feasibility, coverage, acceptability, quality, and effectiveness of the HIVST intervention.</p><p><strong>Results: </strong>An average of 793 MSM received 1,041 HIVST kits on a monthly basis through different distribution channels. Of those who received HIVST kits, 67% were distributed to infrequent testers and non-testers. Testing frequency among users increased to 82% for those who had a recent test during the previous three months, compared to 58% of HIVST non-users. There was a high linkage to care and treatment services (84%) among those who tested reactive for HIV at endline. MSM shared preferring HIVST kits because of its convenience and privacy. During the COVID-19 pandemic, adaptations to the intervention were made to support ongoing HIV testing and linkages to services.</p><p><strong>Conclusion: </strong>The introduction of HIVST in MSM-led HIV prevention programmes was feasible with high acceptability. The involvement of the MSM community in the design, implementation and evaluation of the intervention was a key factor to intervention success.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"7 ","pages":"127"},"PeriodicalIF":0.0,"publicationDate":"2024-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11259586/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141733936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nasopharyngeal Dysbiosis Precedes the Development of Lower Respiratory Tract Infections in Young Infants, a Longitudinal Infant Cohort Study. 婴幼儿下呼吸道感染发生前的鼻咽菌群失调,一项婴幼儿队列纵向研究。
Pub Date : 2024-03-20 eCollection Date: 2022-01-01 DOI: 10.12688/gatesopenres.13561.2
Rotem Lapidot, Tyler Faits, Arshad Ismail, Mushal Allam, Zamantungwak Khumalo, William MacLeod, Geoffrey Kwenda, Zachariah Mupila, Ruth Nakazwe, Daniel Segrè, William Evan Johnson, Donald M Thea, Lawrence Mwananyanda, Christopher J Gill

Background: Infants suffering from lower respiratory tract infections (LRTIs) have distinct nasopharyngeal (NP) microbiome profiles that correlate with severity of disease. Whether these profiles precede the infection or are a consequence of it, is unknown. In order to answer this question, longitudinal studies are needed.

Methods: We conducted a retrospective analysis of NP samples collected in a longitudinal birth cohort study of Zambian mother-infant pairs. Samples were collected every two weeks from 1-week through 14-weeks of age. Ten of the infants in the cohort who developed LRTI were matched 1:3 with healthy comparators. We completed 16S rRNA gene sequencing on the samples each of these infants contributed and compared the NP microbiome of the healthy infants to infants who developed LRTI.

Results: The infant NP microbiome maturation was characterized by transitioning from Staphylococcus dominant to respiratory-genera dominant profiles during the first three months of life, similar to what is described in the literature. Interestingly, infants who developed LRTI had distinct NP microbiome characteristics before infection, in most cases as early as the first week of life. Their NP microbiome was characterized by the presence of Novosphingobium, Delftia, high relative abundance of Anaerobacillus, Bacillus, and low relative abundance of Dolosigranulum, compared to the healthy controls. Mothers of infants with LRTI also had low relative abundance of Dolosigranulum in their baseline samples compared to mothers of infants that did not develop an LRTI.

Conclusions: Our results suggest that specific characteristics of the NP microbiome precede LRTI in young infants and may be present in their mothers as well. Early dysbiosis may play a role in the causal pathway leading to LRTI or could be a marker of underlying immunological, environmental, or genetic characteristics that predispose to LRTI.

背景:患有下呼吸道感染(LRTI)的婴儿有独特的鼻咽(NP)微生物组特征,这些特征与疾病的严重程度相关。这些特征是在感染之前就存在还是感染的结果尚不清楚。为了回答这个问题,需要进行纵向研究:我们对赞比亚母婴出生队列纵向研究中收集的 NP 样本进行了回顾性分析。从婴儿出生 1 周到 14 周期间,每两周采集一次样本。队列中 10 名患 LRTI 的婴儿与健康对照组进行了 1:3 的配对。我们对这些婴儿各自提供的样本进行了 16S rRNA 基因测序,并将健康婴儿的 NP 微生物组与发生 LRTI 的婴儿进行了比较:婴儿 NP 微生物组成熟的特点是在出生后的头三个月从葡萄球菌为主过渡到呼吸道菌群为主,这与文献中描述的情况类似。有趣的是,患 LRTI 的婴儿在感染前就有明显的 NP 微生物组特征,大多数情况下早在出生后第一周就有了。与健康对照组相比,他们的NP微生物组的特点是存在新磷脂菌、Delftia、高相对丰度的厌氧芽孢杆菌、芽孢杆菌和低相对丰度的Dolosigranulum。与未患 LRTI 的婴儿母亲相比,患 LRTI 的婴儿母亲的基线样本中 Dolosigranulum 的相对丰度也较低:我们的研究结果表明,NP 微生物组的特定特征先于幼婴的 LRTI,而且可能也存在于他们的母亲体内。早期的菌群失调可能在导致 LRTI 的因果关系中发挥作用,也可能是导致 LRTI 的潜在免疫、环境或遗传特征的标志。
{"title":"Nasopharyngeal Dysbiosis Precedes the Development of Lower Respiratory Tract Infections in Young Infants, a Longitudinal Infant Cohort Study.","authors":"Rotem Lapidot, Tyler Faits, Arshad Ismail, Mushal Allam, Zamantungwak Khumalo, William MacLeod, Geoffrey Kwenda, Zachariah Mupila, Ruth Nakazwe, Daniel Segrè, William Evan Johnson, Donald M Thea, Lawrence Mwananyanda, Christopher J Gill","doi":"10.12688/gatesopenres.13561.2","DOIUrl":"https://doi.org/10.12688/gatesopenres.13561.2","url":null,"abstract":"<p><strong>Background: </strong>Infants suffering from lower respiratory tract infections (LRTIs) have distinct nasopharyngeal (NP) microbiome profiles that correlate with severity of disease. Whether these profiles precede the infection or are a consequence of it, is unknown. In order to answer this question, longitudinal studies are needed.</p><p><strong>Methods: </strong>We conducted a retrospective analysis of NP samples collected in a longitudinal birth cohort study of Zambian mother-infant pairs. Samples were collected every two weeks from 1-week through 14-weeks of age. Ten of the infants in the cohort who developed LRTI were matched 1:3 with healthy comparators. We completed 16S rRNA gene sequencing on the samples each of these infants contributed and compared the NP microbiome of the healthy infants to infants who developed LRTI.</p><p><strong>Results: </strong>The infant NP microbiome maturation was characterized by transitioning from <i>Staphylococcus</i> dominant to respiratory-genera dominant profiles during the first three months of life, similar to what is described in the literature. Interestingly, infants who developed LRTI had distinct NP microbiome characteristics before infection, in most cases as early as the first week of life. Their NP microbiome was characterized by the presence of <i>Novosphingobium, Delftia</i>, high relative abundance of <i>Anaerobacillus, Bacillus</i>, and low relative abundance of <i>Dolosigranulum,</i> compared to the healthy controls. Mothers of infants with LRTI also had low relative abundance of <i>Dolosigranulum</i> in their baseline samples compared to mothers of infants that did not develop an LRTI.</p><p><strong>Conclusions: </strong>Our results suggest that specific characteristics of the NP microbiome precede LRTI in young infants and may be present in their mothers as well. Early dysbiosis may play a role in the causal pathway leading to LRTI or could be a marker of underlying immunological, environmental, or genetic characteristics that predispose to LRTI.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"6 ","pages":"48"},"PeriodicalIF":0.0,"publicationDate":"2024-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11266592/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141758200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Perceptions and experiences of intravenous iron treatment for anaemia in pregnancy in Malawi: a formative qualitative study. 马拉维孕期贫血患者对静脉注射铁剂治疗的看法和经验:一项形成性定性研究。
Pub Date : 2024-03-08 eCollection Date: 2022-01-01 DOI: 10.12688/gatesopenres.13631.2
Lucinda Manda-Taylor, Macdonald Kufankomwe, Gertrude Chatha, Effie Chipeta, Elisabeth Mamani-Mategula, Martin N Mwangi, Magaret Kelaher, Khic-Houy Prang, Ricardo Ataíde, Sant-Rayn Pasricha, Kamija Samuel Phiri

Background: The study objective was to explore opinions, identify experiences, and describe perspectives on the acceptability of intravenous (IV) iron to treat anaemia in pregnancy and identify potential barriers and facilitators of introducing IV iron in the Malawian healthcare system.

Methods: We conducted 15 in-depth interviews and two focus group discussions with pregnant women, and seven in-depth interviews with health workers at a community-based health centre in Blantyre and a tertiary hospital in Zomba.

Results: Most women who used IV iron treatment during the second trimester of pregnancy reported feeling better and stronger after receiving the intervention. Women perceived that IV iron treatment worked faster than oral iron tablets and increased their haemoglobin count. However, cultural beliefs that IV iron treatment will cause miscarriage and the perception that study procedures involved Satanism and vampirism practices were barriers to acceptability. Health workers found IV iron treatment easy to administer because it is a single-dose treatment, simultaneously reducing the burden for pregnant women taking daily oral iron tablets. However, health workers expressed concerns about the costs and the need to train health workers before the large-scale implementation and integration of IV iron treatment into Malawi's routine care.

Conclusions: Despite the perceived concerns and challenges experienced in participating in the first IV iron infusion trial in Malawi, participants' reflections suggest that IV iron infusion is acceptable for treating iron-deficiency anaemia in pregnancy. Participant advocate groups can offer a peer-to-peer education approach to sensitize and engage community members on the benefits of treatment and dispel concerns when the country contemplates integrating IV iron infusion for treating anaemia in pregnancy in Malawi.

背景:本研究旨在探讨马拉维医疗系统中静脉注射铁剂治疗妊娠期贫血的可接受性,确定经验并描述观点,同时确定引入静脉注射铁剂的潜在障碍和促进因素。研究方法我们对孕妇进行了 15 次深入访谈和两次焦点小组讨论,并对布兰太尔一家社区医疗中心和松巴一家三级医院的医护人员进行了 7 次深入访谈。结果大多数在怀孕后三个月使用静脉注射铁剂治疗的妇女表示,在接受干预后感觉更好、更强壮了。妇女们认为静脉注射铁剂治疗见效更快,血红蛋白数量也有所增加。然而,认为静脉注射铁剂治疗会导致流产的文化观念,以及认为研究程序涉及撒旦教和吸血鬼习俗的看法,都是影响接受程度的障碍。医务工作者认为静脉注射铁剂治疗易于操作,因为它是一种单剂量治疗,同时减轻了孕妇每天口服铁剂的负担。不过,医务工作者对成本表示担忧,并认为在大规模实施静脉注射铁剂治疗并将其纳入马拉维的常规护理之前,需要对医务工作者进行培训。结论:尽管参与马拉维首次静脉输注铁剂试验过程中遇到了一些顾虑和挑战,但参与者的反思表明,静脉输注铁剂治疗妊娠期缺铁性贫血是可以接受的。当马拉维考虑将静脉输注铁剂用于治疗妊娠期贫血时,参与者倡导小组可以提供一种同伴教育方法,让社区成员了解治疗的益处,并消除他们的顾虑。
{"title":"Perceptions and experiences of intravenous iron treatment for anaemia in pregnancy in Malawi: a formative qualitative study.","authors":"Lucinda Manda-Taylor, Macdonald Kufankomwe, Gertrude Chatha, Effie Chipeta, Elisabeth Mamani-Mategula, Martin N Mwangi, Magaret Kelaher, Khic-Houy Prang, Ricardo Ataíde, Sant-Rayn Pasricha, Kamija Samuel Phiri","doi":"10.12688/gatesopenres.13631.2","DOIUrl":"10.12688/gatesopenres.13631.2","url":null,"abstract":"<p><strong>Background: </strong>The study objective was to explore opinions, identify experiences, and describe perspectives on the acceptability of intravenous (IV) iron to treat anaemia in pregnancy and identify potential barriers and facilitators of introducing IV iron in the Malawian healthcare system.</p><p><strong>Methods: </strong>We conducted 15 in-depth interviews and two focus group discussions with pregnant women, and seven in-depth interviews with health workers at a community-based health centre in Blantyre and a tertiary hospital in Zomba.</p><p><strong>Results: </strong>Most women who used IV iron treatment during the second trimester of pregnancy reported feeling better and stronger after receiving the intervention. Women perceived that IV iron treatment worked faster than oral iron tablets and increased their haemoglobin count. However, cultural beliefs that IV iron treatment will cause miscarriage and the perception that study procedures involved Satanism and vampirism practices were barriers to acceptability. Health workers found IV iron treatment easy to administer because it is a single-dose treatment, simultaneously reducing the burden for pregnant women taking daily oral iron tablets. However, health workers expressed concerns about the costs and the need to train health workers before the large-scale implementation and integration of IV iron treatment into Malawi's routine care.</p><p><strong>Conclusions: </strong>Despite the perceived concerns and challenges experienced in participating in the first IV iron infusion trial in Malawi, participants' reflections suggest that IV iron infusion is acceptable for treating iron-deficiency anaemia in pregnancy. Participant advocate groups can offer a peer-to-peer education approach to sensitize and engage community members on the benefits of treatment and dispel concerns when the country contemplates integrating IV iron infusion for treating anaemia in pregnancy in Malawi.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"6 ","pages":"66"},"PeriodicalIF":0.0,"publicationDate":"2024-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10917769/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140059114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Taking stock: Is gene drive research delivering on its principles? 盘点:基因驱动研究是否符合其原则?
Pub Date : 2024-02-22 eCollection Date: 2024-01-01 DOI: 10.12688/gatesopenres.15323.1
Aaron J Roberts, Kristy Hackett, Isabelle Coche, Stephanie L James, Katherine Littler, Michael Santos, Claudia I Emerson

Gene drive technology has been recognized for its potential to provide durable and cost-effective solutions for previously intractable problems in public health, conservation, and agriculture. In recognition of the rapid advances in this field, in 2016 the U.S. National Academies of Sciences, Engineering, and Medicine issued a report making several recommendations aimed at researchers, funders, and policymakers for the safe and responsible research and development of gene drive technology. Subsequently, in 2017 sixteen global organizations self-identifying as sponsors and supporters of gene drive research became public signatories committed to the 'Principles for Gene Drive Research' which were inspired by the report's recommendations. Herein we reflect on the progress of gene drive research in relation to the ethical principles laid out and committed to by the signatories to the Principles. Our analysis indicates high levels of alignment with the Principles in the field of gene drive research. The manuscript also discusses the Gene Drive Research Forum, which had its genesis in the publication of the Principles. Discussions between participants at the latest meeting of the Forum point to the work that lies ahead for gene drive research in line with the Principles. Going forward the gene drive research community can productively focus on: i) safety and efficacy criteria for open release, ii) risk assessment frameworks and methods, iii) more downstream technical, regulatory and policy considerations for field evaluations and implementation, iv) continued transparency and developing mechanisms of accountability, and v) strengthening capacity in locales of potential release and expected drive spread.

基因驱动技术已被公认为具有潜力,可为公共卫生、自然保护和农业领域以往难以解决的问题提供持久且具有成本效益的解决方案。鉴于该领域的快速发展,美国国家科学院、工程院和医学院于 2016 年发布了一份报告,针对研究人员、资助者和政策制定者提出了多项建议,以安全、负责任地研发基因驱动技术。随后,在报告建议的启发下,16 个自我认定为基因驱动研究赞助者和支持者的全球性组织于 2017 年成为 "基因驱动研究原则 "的公开签署方。在此,我们结合原则签署方制定和承诺的伦理原则,对基因驱动研究的进展情况进行反思。我们的分析表明,基因驱动研究领域与《原则》高度一致。手稿还讨论了基因驱动研究论坛,该论坛的起源正是《原则》的发布。在论坛最近一次会议上,与会者进行了讨论,指出了根据《原则》开展基因驱动研究的未来工作。展望未来,基因驱动研究界可将工作重点放在以下方面:i) 公开释放的安全性和有效性标准;ii) 风险评估框架和方法;iii) 实地评估和实施的更多下游技术、监管和政策考虑因素;iv) 持续的透明度和发展问责机制;v) 加强潜在释放地和预期驱动传播地的能力。
{"title":"Taking stock: Is gene drive research delivering on its principles?","authors":"Aaron J Roberts, Kristy Hackett, Isabelle Coche, Stephanie L James, Katherine Littler, Michael Santos, Claudia I Emerson","doi":"10.12688/gatesopenres.15323.1","DOIUrl":"10.12688/gatesopenres.15323.1","url":null,"abstract":"<p><p>Gene drive technology has been recognized for its potential to provide durable and cost-effective solutions for previously intractable problems in public health, conservation, and agriculture. In recognition of the rapid advances in this field, in 2016 the U.S. National Academies of Sciences, Engineering, and Medicine issued a report making several recommendations aimed at researchers, funders, and policymakers for the safe and responsible research and development of gene drive technology. Subsequently, in 2017 sixteen global organizations self-identifying as sponsors and supporters of gene drive research became public signatories committed to the 'Principles for Gene Drive Research' which were inspired by the report's recommendations. Herein we reflect on the progress of gene drive research in relation to the ethical principles laid out and committed to by the signatories to the Principles. Our analysis indicates high levels of alignment with the Principles in the field of gene drive research. The manuscript also discusses the Gene Drive Research Forum, which had its genesis in the publication of the Principles. Discussions between participants at the latest meeting of the Forum point to the work that lies ahead for gene drive research in line with the Principles. Going forward the gene drive research community can productively focus on: i) safety and efficacy criteria for open release, ii) risk assessment frameworks and methods, iii) more downstream technical, regulatory and policy considerations for field evaluations and implementation, iv) continued transparency and developing mechanisms of accountability, and v) strengthening capacity in locales of potential release and expected drive spread.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"8 ","pages":"14"},"PeriodicalIF":0.0,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11259591/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141733938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study of helminth eggs ( Ascaris suum) inactivation by anaerobic digestion and electrochemical treatment. 通过厌氧消化和电化学处理灭活蠕虫卵(蛔虫)的研究。
Pub Date : 2024-02-12 eCollection Date: 2023-01-01 DOI: 10.12688/gatesopenres.14573.2
Prajakta Pratap Patil, Srikanth Mutnuri

Background: The use of insufficiently treated wastewater or Faecal sludge in agriculture raises concerns because of the pathogen content. Helminth eggs (HE) are one of the most crucial pathogens for ensuring public health and safety. Widely used disinfection treatment methods do not guarantee the complete inactivation of helminth eggs. The current study evaluated the effectiveness of anaerobic digestion and electrochemical process on helminth ( Ascaris suum) egg inactivation.

Methods: Lab-scale biochemical methane potential (BMP) assay was conducted by spiking A. suum eggs in a serum bottle. Total solid (TS), volatile solid (VS), pH, biogas production and its composition, and volatile fatty acids (VFA) were analyzed along with A. suum inactivation every third day for the initial 15 days and fifth day for 45 days. In the second set of experiments, a hypochlorite (4700 ppm) solution was generated by electrolysis of aqueous NaCl solution in a membrane-less electrochemical cell. The hypochlorite was diluted (940, 470, 235, and 156ppm) in wastewater, spiked with A. suum eggs and then examined for inactivation at regular intervals.

Results: The results of the anaerobic digestion treatment documented 98% inactivation of A. suum eggs (0.15 eggs/mL) in 35 days and remained at 0.14 eggs/mL until day 45. Correlation analysis revealed a positive relationship between non-viable eggs and pH and a negative relationship with all the other parameters. Electrochemical treatment achieved 10% inactivation at 940 ppm concentration in 24h.

Conclusions: This study revealed that the inactivation of A. suum eggs by anaerobic digestion or electrochemical treatment is a combined effect of more than one parameter.

背景:在农业中使用未经充分处理的废水或粪便污泥因其含有病原体而引起人们的关注。蠕虫卵(HE)是确保公众健康和安全的最重要病原体之一。广泛使用的消毒处理方法并不能保证完全灭活螺旋虫卵。本研究评估了厌氧消化和电化学处理对蠕虫卵灭活的效果:方法:在血清瓶中加入蛔虫卵,进行实验室规模的生化甲烷潜能(BMP)测定。在最初的 15 天内,每隔 3 天分析一次总固体(TS)、挥发性固体(VS)、pH 值、沼气产量及其成分和挥发性脂肪酸(VFA),45 天内每隔 5 天分析一次蛔虫灭活情况。在第二组实验中,无膜电化学电池通过电解氯化钠水溶液产生次氯酸盐溶液(4700 ppm)。在废水中稀释次氯酸盐(940、470、235 和 156ppm),并在其中添加恙虫卵,然后定期检查灭活情况:结果:厌氧消化处理的结果表明,35 天内鼠卵的灭活率为 98%(0.15 个卵/毫升),直到第 45 天仍为 0.14 个卵/毫升。相关分析表明,不能存活的虫卵与 pH 值呈正相关,而与所有其他参数呈负相关。电化学处理可在 24 小时内灭活浓度为 940 ppm 的 10%的虫卵:这项研究表明,厌氧消化或电化学处理对鼠卵的灭活是多个参数共同作用的结果。
{"title":"Study of helminth eggs ( <i>Ascaris suum)</i> inactivation by anaerobic digestion and electrochemical treatment.","authors":"Prajakta Pratap Patil, Srikanth Mutnuri","doi":"10.12688/gatesopenres.14573.2","DOIUrl":"https://doi.org/10.12688/gatesopenres.14573.2","url":null,"abstract":"<p><strong>Background: </strong>The use of insufficiently treated wastewater or Faecal sludge in agriculture raises concerns because of the pathogen content. Helminth eggs (HE) are one of the most crucial pathogens for ensuring public health and safety. Widely used disinfection treatment methods do not guarantee the complete inactivation of helminth eggs. The current study evaluated the effectiveness of anaerobic digestion and electrochemical process on helminth ( <i>Ascaris suum</i>) egg inactivation.</p><p><strong>Methods: </strong>Lab-scale biochemical methane potential (BMP) assay was conducted by spiking <i>A. suum</i> eggs in a serum bottle. Total solid (TS), volatile solid (VS), pH, biogas production and its composition, and volatile fatty acids (VFA) were analyzed along with <i>A. suum</i> inactivation every third day for the initial 15 days and fifth day for 45 days. In the second set of experiments, a hypochlorite (4700 ppm) solution was generated by electrolysis of aqueous NaCl solution in a membrane-less electrochemical cell. The hypochlorite was diluted (940, 470, 235, and 156ppm) in wastewater, spiked with <i>A. suum</i> eggs and then examined for inactivation at regular intervals.</p><p><strong>Results: </strong>The results of the anaerobic digestion treatment documented 98% inactivation of <i>A. suum</i> eggs (0.15 eggs/mL) in 35 days and remained at 0.14 eggs/mL until day 45. Correlation analysis revealed a positive relationship between non-viable eggs and pH and a negative relationship with all the other parameters. Electrochemical treatment achieved 10% inactivation at 940 ppm concentration in 24h.</p><p><strong>Conclusions: </strong>This study revealed that the inactivation of <i>A. suum</i> eggs by anaerobic digestion or electrochemical treatment is a combined effect of more than one parameter.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"7 ","pages":"93"},"PeriodicalIF":0.0,"publicationDate":"2024-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11422576/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142344902","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison of Masimo Total Hemoglobin SpHb® continuous non-invasive hemoglobin monitoring device with laboratory complete blood count measurement using venous sample: Protocol for an observational substudy of the Pregnancy Risk and Infant Surveillance and Measurement Alliance Maternal and Newborn Health (PRISMA MNH) study. Masimo总血红蛋白SpHb®连续无创血红蛋白监测设备与使用静脉样本的实验室全血细胞计数测量的比较:妊娠风险和婴儿监测与测量联盟母婴健康(PRISMA MNH)研究的观察性亚研究方案。
Pub Date : 2024-02-05 eCollection Date: 2023-01-01 DOI: 10.12688/gatesopenres.14499.1
Fouzia Farooq, Emily R Smith, Qing Pan, Sasha Glass Baumann, Victor Akelo, Fyezah Jehan, Margaret Kasaro, Imran Nisar, Gregory Ouma, Bellington Vwalika, M Bridget Spelke, Joan T Price, Zahra Hoodbhoy

Background: The Masimo Total Hemoglobin SpHb® is a continuous and non-invasive handheld device to measure hemoglobin levels. Previous research has found that SpHb is able to accurately detect hemoglobin levels in adult patients with a similar degree of bias and standard deviation to point-of-care invasive method measurements. Generally, limited clinical evidence, lack of validation of Masimo at higher than and lower than hemoglobin threshold values, and scientific consensus supporting the use of Masimo for accurate hemoglobin testing for the diagnosis of anemia during pregnancy calls for further research.

Methods and analysis: The proposed prospective cohort will be nested within the ongoing Pregnancy Risk and Infant Surveillance and Measurement Alliance (PRISMA) Maternal and Newborn Health (MNH) study. Three study sites (located in Zambia, Kenya, and Pakistan) will participate and collect hemoglobin data at five time points (<20 weeks, 20 weeks, 28 weeks, 36 weeks' gestation, and six weeks postpartum). We will measure hemoglobin using a venous blood sample via hematology auto-analyzer complete blood count (gold standard) and the non-invasive device. The primary objective is to assess agreement between Masimo total hemoglobin and complete blood count and on a continuous scale using Intraclass Correlation Coefficient and Bland-Altman Analysis. The second objective is to assess agreement between the two measures on a binary scale using Positive Percentage Agreement and Negative Percentage Agreement, Cohen's Kappa, and McNemar Test. On an ordinal scale, agreement will be measured using Weighted Cohen's Kappa and Harrel's Concordance Index. Lastly, we will assess factors that might affect the accuracy of Masimo total hemoglobin using linear mixed models.

Conclusions: The primary aim of this study is to assess the validity of the non-invasive Masimo device compared to the gold standard method of invasive hemoglobin measurements during pregnancy and postpartum periods for the diagnosis of anemia.

背景:Masimo Total Hemoglobin SpHb®是一种用于测量血红蛋白水平的连续无创手持设备。先前的研究发现,SpHb能够准确检测成年患者的血红蛋白水平,其偏差和标准偏差与护理点侵入性方法测量的偏差和标准差相似。一般来说,临床证据有限,Masimo在高于和低于血红蛋白阈值时缺乏验证,以及支持使用Masimo进行准确的血红蛋白检测以诊断妊娠期贫血的科学共识,都需要进一步研究。方法和分析:拟议的前瞻性队列将嵌套在正在进行的妊娠风险和婴儿监测与测量联盟(PRISMA)母婴健康(MNH)研究中。三个研究地点(位于赞比亚、肯尼亚和巴基斯坦)将参与并收集五个时间点的血红蛋白数据(结论:本研究的主要目的是评估无创Masimo设备与妊娠期和产后有创血红蛋白测量金标准方法相比诊断贫血的有效性。
{"title":"Comparison of Masimo Total Hemoglobin SpHb® continuous non-invasive hemoglobin monitoring device with laboratory complete blood count measurement using venous sample: Protocol for an observational substudy of the Pregnancy Risk and Infant Surveillance and Measurement Alliance Maternal and Newborn Health (PRISMA MNH) study.","authors":"Fouzia Farooq, Emily R Smith, Qing Pan, Sasha Glass Baumann, Victor Akelo, Fyezah Jehan, Margaret Kasaro, Imran Nisar, Gregory Ouma, Bellington Vwalika, M Bridget Spelke, Joan T Price, Zahra Hoodbhoy","doi":"10.12688/gatesopenres.14499.1","DOIUrl":"10.12688/gatesopenres.14499.1","url":null,"abstract":"<p><strong>Background: </strong>The Masimo Total Hemoglobin SpHb® is a continuous and non-invasive handheld device to measure hemoglobin levels. Previous research has found that SpHb is able to accurately detect hemoglobin levels in adult patients with a similar degree of bias and standard deviation to point-of-care invasive method measurements. Generally, limited clinical evidence, lack of validation of Masimo at higher than and lower than hemoglobin threshold values, and scientific consensus supporting the use of Masimo for accurate hemoglobin testing for the diagnosis of anemia during pregnancy calls for further research.</p><p><strong>Methods and analysis: </strong>The proposed prospective cohort will be nested within the ongoing Pregnancy Risk and Infant Surveillance and Measurement Alliance (PRISMA) Maternal and Newborn Health (MNH) study. Three study sites (located in Zambia, Kenya, and Pakistan) will participate and collect hemoglobin data at five time points (<20 weeks, 20 weeks, 28 weeks, 36 weeks' gestation, and six weeks postpartum). We will measure hemoglobin using a venous blood sample via hematology auto-analyzer complete blood count (gold standard) and the non-invasive device. The primary objective is to assess agreement between Masimo total hemoglobin and complete blood count and on a continuous scale using Intraclass Correlation Coefficient and Bland-Altman Analysis. The second objective is to assess agreement between the two measures on a binary scale using Positive Percentage Agreement and Negative Percentage Agreement, Cohen's Kappa, and McNemar Test. On an ordinal scale, agreement will be measured using Weighted Cohen's Kappa and Harrel's Concordance Index. Lastly, we will assess factors that might affect the accuracy of Masimo total hemoglobin using linear mixed models.</p><p><strong>Conclusions: </strong>The primary aim of this study is to assess the validity of the non-invasive Masimo device compared to the gold standard method of invasive hemoglobin measurements during pregnancy and postpartum periods for the diagnosis of anemia.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"7 ","pages":"50"},"PeriodicalIF":0.0,"publicationDate":"2024-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587393/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49689892","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
National health insurance contribution to family planning program funding in Indonesia: A fund flow analysis. 印度尼西亚国家医疗保险对计划生育计划资金的贡献:资金流分析。
Pub Date : 2024-01-18 eCollection Date: 2023-01-01 DOI: 10.12688/gatesopenres.14642.2
Amirah Ellyza Wahdi, Edward Sutanto, Althaf Setyawan, Yufan Putri Astrini, Nadhila Adani, Halimah Mardani, Nirwan Maulana, Anooj Pattnaik, Trihono Trihono, Siswanto Agus Wilopo

Background: Launched in 2014, Indonesia's national health insurance system (JKN) aimed to provide universal health coverage, including contraceptive services, to its population. We aim to evaluate the contribution of JKN to the overall spending for the family planning program in Indonesia.

Methods: Data from the Indonesian Demographic Health Survey, Survey on Financial Flows for Family Planning, Indonesia Motion Tracker Matrix, World Population Prospect, and Indonesian ministries' budget accountability reports were entered into the CastCost Contraceptive Projection Tool to define budgetary allocation and spending for the family planning program at the national level in 2019.

Results: Indonesia's family planning program in 2019 was financed mostly by the national budget (64.0%) and out-of-pocket payments (34.6%). There were three main ministries responsible for family planning financing: the National Population and Family Planning Board (BKKBN) (35.8%), the Ministry of Finance (26.2%), and the Ministry of Health (2.0%). Overall, JKN contributed less than 0.4% of the funding for family planning services in Indonesia in 2019. The majority of family planning spending was by public facilities (57.3%) as opposed to private facilities (28.6%).

Conclusion: JKN's contribution to funding Indonesia's family planning programs in 2019 was low and highlights a huge opportunity to expand these contributions. A coordinated effort should be conducted to identify possible opportunities to realign BKKBN and JKN roles in the family planning programs and lift barriers to accessing family planning services in public and private facilities. This includes a concerted effort to improve integration of private family planning providers into the JKN program.

背景:印度尼西亚的国家医疗保险体系(JKN)于 2014 年启动,旨在为其人口提供包括避孕服务在内的全民医疗保险。我们旨在评估印尼国家医疗保险体系对印尼计划生育项目总体支出的贡献:将印尼人口健康调查、计划生育资金流调查、印尼运动追踪矩阵、世界人口展望以及印尼各部委预算问责报告中的数据输入 CastCost 避孕药具预测工具,以确定 2019 年全国计划生育项目的预算分配和支出:印度尼西亚 2019 年计划生育计划的资金主要来自国家预算(64.0%)和自费项目(34.6%)。负责计划生育筹资的主要有三个部委:国家人口和计划生育委员会(BKKBN)(35.8%)、财政部(26.2%)和卫生部(2.0%)。总体而言,2019 年,JKKBN 为印尼计划生育服务提供的资金不足 0.4%。大部分计划生育支出用于公共设施(57.3%),而非私营设施(28.6%):2019年,JKN对印尼计划生育项目的资金贡献率较低,这凸显了扩大这些贡献的巨大机会。应开展协调努力,找出可能的机会,重新调整 BKKBN 和 JKN 在计划生育项目中的作用,并消除在公共和私营机构获得计划生育服务的障碍。这包括共同努力,将私营计划生育服务提供者更好地纳入 JKN 计划。
{"title":"National health insurance contribution to family planning program funding in Indonesia: A fund flow analysis.","authors":"Amirah Ellyza Wahdi, Edward Sutanto, Althaf Setyawan, Yufan Putri Astrini, Nadhila Adani, Halimah Mardani, Nirwan Maulana, Anooj Pattnaik, Trihono Trihono, Siswanto Agus Wilopo","doi":"10.12688/gatesopenres.14642.2","DOIUrl":"10.12688/gatesopenres.14642.2","url":null,"abstract":"<p><strong>Background: </strong>Launched in 2014, Indonesia's national health insurance system (JKN) aimed to provide universal health coverage, including contraceptive services, to its population. We aim to evaluate the contribution of JKN to the overall spending for the family planning program in Indonesia.</p><p><strong>Methods: </strong>Data from the Indonesian Demographic Health Survey, Survey on Financial Flows for Family Planning, Indonesia Motion Tracker Matrix, World Population Prospect, and Indonesian ministries' budget accountability reports were entered into the CastCost Contraceptive Projection Tool to define budgetary allocation and spending for the family planning program at the national level in 2019.</p><p><strong>Results: </strong>Indonesia's family planning program in 2019 was financed mostly by the national budget (64.0%) and out-of-pocket payments (34.6%). There were three main ministries responsible for family planning financing: the National Population and Family Planning Board (BKKBN) (35.8%), the Ministry of Finance (26.2%), and the Ministry of Health (2.0%). Overall, JKN contributed less than 0.4% of the funding for family planning services in Indonesia in 2019. The majority of family planning spending was by public facilities (57.3%) as opposed to private facilities (28.6%).</p><p><strong>Conclusion: </strong>JKN's contribution to funding Indonesia's family planning programs in 2019 was low and highlights a huge opportunity to expand these contributions. A coordinated effort should be conducted to identify possible opportunities to realign BKKBN and JKN roles in the family planning programs and lift barriers to accessing family planning services in public and private facilities. This includes a concerted effort to improve integration of private family planning providers into the JKN program.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"7 ","pages":"105"},"PeriodicalIF":0.0,"publicationDate":"2024-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11006955/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140860588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preferences for services in a patient's first six months on antiretroviral therapy for HIV in South Africa and Zambia (PREFER): research protocol for a prospective observational cohort study. 南非和赞比亚艾滋病患者接受抗逆转录病毒疗法前六个月的服务偏好(PREFER):前瞻性观察队列研究的研究方案。
Pub Date : 2024-01-09 eCollection Date: 2023-01-01 DOI: 10.12688/gatesopenres.14682.2
Mhairi Maskew, Vinolia Ntjikelane, Allison Juntunen, Nancy Scott, Mariet Benade, Linda Sande, Pamfred Hasweeka, Prudence Haimbe, Priscilla Lumano-Mulenga, Hilda Shakewelele, Mpande Mukumbwa-Mwenechanya, Sydney Rosen

Background: For patients on HIV treatment in sub-Saharan Africa, the highest risk for loss from care remains the first six months after antiretroviral (ART) initiation, when patients are not yet eligible for differentiated service delivery (DSD) models that offer lower-burden, patient-centred care and thus improve treatment outcomes. To reduce early disengagement from care, the PREFER study will use a sequential mixed-methods approach to describe the characteristics, needs, concerns, and preferences of patients in South Africa and Zambia 0-6 months after ART initiation or re-initiation.

Protocol: PREFER is an observational, prospective cohort study of adults on ART for ≤6 months at 12 public healthcare facilities in Zambia and 18 in South Africa. Its objective is to describe and understand the needs and preferences of initiating and re-initiating ART clients to inform the design of DSD models for the early HIV treatment period, improve early treatment outcomes, and distinguish the barriers encountered by naïve patients from those facing re-initiators. It has four components: 1) survey of clients 0-6 months after ART initiation (identify characteristics and preferences of clients starting ART); 2) follow up through routinely collected medical records for <24 months after enrollment (describe resource utilization and patterns and predictors of engagement in care); 3) focus group discussions and discrete choice experiment (explore reported barriers to and facilitators of retention); and 4) in South Africa only, collection of blood samples (assess the prevalence of ARV metabolites indicating prior ART use).

Conclusions: PREFER aims to understand why the early treatment period is so challenging and how service delivery can be amended to address the obstacles that lead to early disengagement from care. It will generate information about client characteristics and preferences to help respond to patients' needs and design better strategies for service delivery and improve resource allocation going forward.

背景:对于撒哈拉以南非洲地区接受艾滋病治疗的患者来说,在开始接受抗逆转录病毒疗法(ART)治疗后的前六个月内,脱离治疗的风险最高,因为此时患者还没有资格接受差异化服务提供模式(DSD),这种模式可提供负担较低、以患者为中心的治疗,从而改善治疗效果。为了减少早期脱离治疗的情况,PREFER 研究将采用一种连续的混合方法来描述南非和赞比亚患者在开始或重新开始抗逆转录病毒疗法 0-6 个月后的特征、需求、关注点和偏好:PREFER 是一项观察性、前瞻性队列研究,对象是在赞比亚的 12 家公共医疗机构和南非的 18 家公共医疗机构接受抗逆转录病毒疗法不足 6 个月的成人。其目的是描述和了解抗逆转录病毒疗法初试者和再试者的需求和偏好,为设计艾滋病早期治疗的DSD模式提供参考,改善早期治疗效果,并区分初试者和再试者遇到的障碍。它包括四个部分:1) 对开始接受抗逆转录病毒疗法后 0-6 个月的患者进行调查(确定开始接受抗逆转录病毒疗法的患者的特征和偏好);2) 通过常规收集的医疗记录进行跟踪,得出结论:PREFER 旨在了解早期治疗阶段为何如此具有挑战性,以及如何修改服务提供方式以消除导致早期脱离治疗的障碍。它将提供有关客户特征和偏好的信息,以帮助满足患者的需求,设计更好的服务提供策略,改善未来的资源分配。
{"title":"Preferences for services in a patient's first six months on antiretroviral therapy for HIV in South Africa and Zambia (PREFER): research protocol for a prospective observational cohort study.","authors":"Mhairi Maskew, Vinolia Ntjikelane, Allison Juntunen, Nancy Scott, Mariet Benade, Linda Sande, Pamfred Hasweeka, Prudence Haimbe, Priscilla Lumano-Mulenga, Hilda Shakewelele, Mpande Mukumbwa-Mwenechanya, Sydney Rosen","doi":"10.12688/gatesopenres.14682.2","DOIUrl":"10.12688/gatesopenres.14682.2","url":null,"abstract":"<p><strong>Background: </strong>For patients on HIV treatment in sub-Saharan Africa, the highest risk for loss from care remains the first six months after antiretroviral (ART) initiation, when patients are not yet eligible for differentiated service delivery (DSD) models that offer lower-burden, patient-centred care and thus improve treatment outcomes. To reduce early disengagement from care, the PREFER study will use a sequential mixed-methods approach to describe the characteristics, needs, concerns, and preferences of patients in South Africa and Zambia 0-6 months after ART initiation or re-initiation.</p><p><strong>Protocol: </strong>PREFER is an observational, prospective cohort study of adults on ART for ≤6 months at 12 public healthcare facilities in Zambia and 18 in South Africa. Its objective is to describe and understand the needs and preferences of initiating and re-initiating ART clients to inform the design of DSD models for the early HIV treatment period, improve early treatment outcomes, and distinguish the barriers encountered by naïve patients from those facing re-initiators. It has four components: 1) survey of clients 0-6 months after ART initiation (identify characteristics and preferences of clients starting ART); 2) follow up through routinely collected medical records for <24 months after enrollment (describe resource utilization and patterns and predictors of engagement in care); 3) focus group discussions and discrete choice experiment (explore reported barriers to and facilitators of retention); and 4) in South Africa only, collection of blood samples (assess the prevalence of ARV metabolites indicating prior ART use).</p><p><strong>Conclusions: </strong>PREFER aims to understand why the early treatment period is so challenging and how service delivery can be amended to address the obstacles that lead to early disengagement from care. It will generate information about client characteristics and preferences to help respond to patients' needs and design better strategies for service delivery and improve resource allocation going forward.</p>","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"7 ","pages":"119"},"PeriodicalIF":0.0,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10858017/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139722254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Estimating dengue disease and economic burden to inform municipal-level policymakers: Method for a pragmatic city-level observational cohort study 估算登革热疾病和经济负担,为市级决策者提供信息:务实的城市观测队列研究方法
Pub Date : 2024-01-08 DOI: 10.12688/gatesopenres.15015.1
Nandyan N. Wilastonegoro, Sri Andriani, P. Sebong, Priya Agarwal-Harding, Donald S. Shepard
Background Recent trials have confirmed the effectiveness of promising dengue control technologies – two vaccines, and Wolbachia. These would generally be applied at the municipal level. To balance health needs and resource constraints, local officials need affordable, timely, and accurate data. Building on our previous work in Mexico, Indonesia, and Thailand, we developed a streamlined prospective method to estimate dengue burden at the municipal level quickly, accurately, and efficiently. Method The method entails enrolling and repeatedly interviewing 100 patients with laboratory-confirmed dengue. They will be selected after screening and testing about 1,000 patients with clinical dengue. The method will capture both acute and chronic effects relating to disease, economic burden, and psychological impacts (presenteeism). The total time requirements are 1.5 years, comprised of 0.25 years for planning and approvals, 1 year for data collection (a full dengue cycle), and 0 .25 years for data cleaning and analysis. A collaboration with municipal and academic colleagues in the city of Semarang, Central Java, Indonesia shows how the method could be readily applied in Indonesia’s eighth largest city (population 1.8 million). Conclusions Many surveillance studies gather only information on numbers of cases. This proposed method will provide a comprehensive picture of the dengue burden to the health system, payers, and households at the local level.
背景 最近的试验证实了两种疫苗和 Wolbachia 等有前景的登革热控制技术的有效性。这些技术一般会在市一级应用。为了平衡健康需求和资源限制,地方官员需要经济实惠、及时准确的数据。在墨西哥、印度尼西亚和泰国工作的基础上,我们开发了一种简化的前瞻性方法,可以快速、准确、高效地估算市一级的登革热负担。方法 该方法需要招募并反复访问 100 名经实验室确诊的登革热患者。他们将在筛选和检测约 1000 名临床登革热患者后选出。该方法将收集与疾病、经济负担和心理影响(缺勤)有关的急性和慢性影响。所需时间共计 1.5 年,其中 0.25 年用于规划和审批,1 年用于数据收集(一个完整的登革热周期),0.25 年用于数据清理和分析。与印尼中爪哇省三宝垄市的市政和学术界同行合作,展示了如何在这个印尼第八大城市(人口 180 万)应用该方法。结论 许多监测研究只收集病例数量的信息。这种建议的方法将为地方一级的卫生系统、支付者和家庭提供登革热负担的全面情况。
{"title":"Estimating dengue disease and economic burden to inform municipal-level policymakers: Method for a pragmatic city-level observational cohort study","authors":"Nandyan N. Wilastonegoro, Sri Andriani, P. Sebong, Priya Agarwal-Harding, Donald S. Shepard","doi":"10.12688/gatesopenres.15015.1","DOIUrl":"https://doi.org/10.12688/gatesopenres.15015.1","url":null,"abstract":"Background Recent trials have confirmed the effectiveness of promising dengue control technologies – two vaccines, and Wolbachia. These would generally be applied at the municipal level. To balance health needs and resource constraints, local officials need affordable, timely, and accurate data. Building on our previous work in Mexico, Indonesia, and Thailand, we developed a streamlined prospective method to estimate dengue burden at the municipal level quickly, accurately, and efficiently. Method The method entails enrolling and repeatedly interviewing 100 patients with laboratory-confirmed dengue. They will be selected after screening and testing about 1,000 patients with clinical dengue. The method will capture both acute and chronic effects relating to disease, economic burden, and psychological impacts (presenteeism). The total time requirements are 1.5 years, comprised of 0.25 years for planning and approvals, 1 year for data collection (a full dengue cycle), and 0 .25 years for data cleaning and analysis. A collaboration with municipal and academic colleagues in the city of Semarang, Central Java, Indonesia shows how the method could be readily applied in Indonesia’s eighth largest city (population 1.8 million). Conclusions Many surveillance studies gather only information on numbers of cases. This proposed method will provide a comprehensive picture of the dengue burden to the health system, payers, and households at the local level.","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":"58 40","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139446857","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Gates Open Research
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1