Pub Date : 2023-12-01DOI: 10.1080/26410397.2023.2193315
Grace W Kimemia, Caroline W Kabiru, Boniface Ayanbekongshie Ushie
{"title":"Ethical concerns facing abortion researchers in restrictive settings: the need for guidelines.","authors":"Grace W Kimemia, Caroline W Kabiru, Boniface Ayanbekongshie Ushie","doi":"10.1080/26410397.2023.2193315","DOIUrl":"10.1080/26410397.2023.2193315","url":null,"abstract":"","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 1","pages":"2193315"},"PeriodicalIF":3.3,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/21/3d/ZRHM_31_2193315.PMC10134914.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9761943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pandemic mitigation measures can have a negative impact on access and provision of essential healthcare services including sexual and reproductive health (SRH) services. This rapid review looked at the literature on the impact of COVID-19 mitigation measures on SRH and gender-based violence (GBV) on women in low- and middle-income countries (LMIC) using WHO rapid review guidance. We looked at relevant literature published in the English language from January 2020 to October 2021 from LMICs using WHO rapid review methods. A total of 114 articles were obtained from PubMed, Google Scholar and grey literature of which 20 met the eligible criteria. Our review found that there was an overall reduction in; (a) uptake of services as shown by lower antenatal, postnatal and family planning clinic attendance, (b) service delivery as shown by reduced health facility deliveries, and post abortion care services and (c) reproductive health outcomes as shown by an increase in incidence of GBV especially intimate partner violence. COVID-19 mitigation measures negatively impact SRH of women in LMICs. Findings from this review could inform policy makers in the health sector to recognise the potential adverse effects of COVID-19 responses on SRH in the country, and therefore implement mitigation measures.
{"title":"The impact of COVID-19 mitigation measures on sexual and reproductive health in low- and middle-income countries: a rapid review.","authors":"Elizabeth Ochola, Maheshwari Andhavarapu, Poppy Sun, Abdu Mohiddin, Okwaro Ferdinand, Marleen Temmerman","doi":"10.1080/26410397.2023.2203001","DOIUrl":"10.1080/26410397.2023.2203001","url":null,"abstract":"<p><p>Pandemic mitigation measures can have a negative impact on access and provision of essential healthcare services including sexual and reproductive health (SRH) services. This rapid review looked at the literature on the impact of COVID-19 mitigation measures on SRH and gender-based violence (GBV) on women in low- and middle-income countries (LMIC) using WHO rapid review guidance. We looked at relevant literature published in the English language from January 2020 to October 2021 from LMICs using WHO rapid review methods. A total of 114 articles were obtained from PubMed, Google Scholar and grey literature of which 20 met the eligible criteria. Our review found that there was an overall reduction in; (a) uptake of services as shown by lower antenatal, postnatal and family planning clinic attendance, (b) service delivery as shown by reduced health facility deliveries, and post abortion care services and (c) reproductive health outcomes as shown by an increase in incidence of GBV especially intimate partner violence. COVID-19 mitigation measures negatively impact SRH of women in LMICs. Findings from this review could inform policy makers in the health sector to recognise the potential adverse effects of COVID-19 responses on SRH in the country, and therefore implement mitigation measures.</p>","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 1","pages":"2203001"},"PeriodicalIF":3.3,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d7/d0/ZRHM_31_2203001.PMC10259330.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9981869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2023-10-23DOI: 10.1080/26410397.2023.2261681
David Aduragbemi Okunlola, Oluwatobi Abel Alawode, Abayomi Folorunso Awoleye, Benjamin Bukky Ilesanmi
Digital health interventions are gaining ground in conflict-affected countries, but studies on their reproductive health benefits for women are scanty. Focusing on conflict-affected northern Nigeria, this study examined the relationships between Internet use, exposure to digital family planning messages via text messages or social media, and sexual agency - measured as the ability to refuse sex and ask a male partner to use a condom - among partnered women including the rural-urban differentials. Partnered women's data (n= 18,205) from the 2018 Nigeria Demographic and Health Survey were analysed using descriptive and multinomial logistic regression analyses. 44.6% of women are able to refuse sex, and 31.4% to ask a male partner to use a condom. Internet use was positively associated with women's ability to refuse sex in the northern region and urban areas, and across the region to ask a male partner to use a condom. It was also positively associated with women's uncertainty about asking a male partner to use a condom. Exposure to digital family planning messages was positively associated with women's ability to ask a male partner to use a condom across the region, in both urban and rural areas. However, exposure to digital family planning messages was negatively associated with women's uncertainty in urban areas about their ability to refuse sex. Implications of these findings for digital family planning interventions are discussed.
{"title":"Internet use, exposure to digital family planning messages, and sexual agency among partnered women in Northern Nigeria: implications for digital family planning intervention.","authors":"David Aduragbemi Okunlola, Oluwatobi Abel Alawode, Abayomi Folorunso Awoleye, Benjamin Bukky Ilesanmi","doi":"10.1080/26410397.2023.2261681","DOIUrl":"10.1080/26410397.2023.2261681","url":null,"abstract":"<p><p>Digital health interventions are gaining ground in conflict-affected countries, but studies on their reproductive health benefits for women are scanty. Focusing on conflict-affected northern Nigeria, this study examined the relationships between Internet use, exposure to digital family planning messages via text messages or social media, and sexual agency - measured as the ability to refuse sex and ask a male partner to use a condom - among partnered women including the rural-urban differentials. Partnered women's data (n= 18,205) from the 2018 Nigeria Demographic and Health Survey were analysed using descriptive and multinomial logistic regression analyses. 44.6% of women are able to refuse sex, and 31.4% to ask a male partner to use a condom. Internet use was positively associated with women's ability to refuse sex in the northern region and urban areas, and across the region to ask a male partner to use a condom. It was also positively associated with women's uncertainty about asking a male partner to use a condom. Exposure to digital family planning messages was positively associated with women's ability to ask a male partner to use a condom across the region, in both urban and rural areas. However, exposure to digital family planning messages was negatively associated with women's uncertainty in urban areas about their ability to refuse sex. Implications of these findings for digital family planning interventions are discussed.</p>","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 4","pages":"2261681"},"PeriodicalIF":6.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/71/a9/ZRHM_31_2261681.PMC10595375.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49692752","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2024-03-25DOI: 10.1080/26410397.2024.2310889
Maribel Mella-Guzmán, Lorena Binfa, Fiona Weeks
The medicalisation of childbirth has diminished the role of labouring people. We conducted an exploratory phenomenological qualitative study, using purposive sampling, and then conducted 17 semi-structured interviews between December 2016 and October 2017 with people who had recently given birth in a public hospital in the Northern Metropolitan area of Santiago, Chile. The sufficiency of the study group was determined according to saturation criteria. Triangulated content analysis was applied to explore the clinical relationship and processes of autonomy and decision-making. The predominant clinical relationship observed was paternalism. The participation of labouring people in decision-making is scarce, with no evidence of ethically valid processes of informed consent.
{"title":"Autonomy in labour and delivery in a Latin American urban centre: a qualitative phenomenological analysis.","authors":"Maribel Mella-Guzmán, Lorena Binfa, Fiona Weeks","doi":"10.1080/26410397.2024.2310889","DOIUrl":"10.1080/26410397.2024.2310889","url":null,"abstract":"<p><p>The medicalisation of childbirth has diminished the role of labouring people. We conducted an exploratory phenomenological qualitative study, using purposive sampling, and then conducted 17 semi-structured interviews between December 2016 and October 2017 with people who had recently given birth in a public hospital in the Northern Metropolitan area of Santiago, Chile. The sufficiency of the study group was determined according to saturation criteria. Triangulated content analysis was applied to explore the clinical relationship and processes of autonomy and decision-making. The predominant clinical relationship observed was paternalism. The participation of labouring people in decision-making is scarce, with no evidence of ethically valid processes of informed consent.</p>","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 1","pages":"2310889"},"PeriodicalIF":6.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10964828/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140289115","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2023-11-20DOI: 10.1080/26410397.2023.2274667
Amnesty LeFevre, Olivia Welte, Kearabetswe Moopelo, Nicki Tiffin, Gaolatlhe Mothoagae, Nobukhosi Ncube, Nasiphi Gwiji, Manape Shogole, Amy L Slogrove, Nomakhawuta Moshani, Andrew Boulle, Jane Goudge, Frances Griffiths, Lee Fairlie, Ushma Mehta, Kerry Scott, Nirvana Pillay
Despite the expanding digitisation of individual health data, informed consent for the collection and use of health data is seldom explicitly sought in public sector clinics in South Africa. This study aims to identify perceptions of informed consent practices for health data capture, access, and use in Gauteng and the Western Cape provinces of South Africa. Data collection from September to December 2021 included in-depth interviews with healthcare providers (n = 12) and women (n = 62) attending maternity services. Study findings suggest that most patients were not aware that their data were being used for purposes beyond the individualised provision of medical care. Understanding the concept of anonymised use of electronic health data was at times challenging for patients who understood their data in the limited context of paper-based folders and booklets. When asked about preferences for electronic data, patients overwhelmingly were in favour of digitisation. They viewed electronic access to their health data as facilitating rapid and continuous access to health information. Patients were additionally asked about preferences, including delivery of health information, onward health data use, and recontacting. Understanding of these use cases varied and was often challenging to convey to participants who understood their health data in the context of information inputted into their paper folders. Future systems need to be established to collect informed consent for onward health data use. In light of perceived ties to the care received, these systems need to ensure that patient preferences do not impede the content nor quality of care received.
{"title":"Preferences for onward health data use in the electronic age among maternity patients and providers in South Africa: a qualitative study.","authors":"Amnesty LeFevre, Olivia Welte, Kearabetswe Moopelo, Nicki Tiffin, Gaolatlhe Mothoagae, Nobukhosi Ncube, Nasiphi Gwiji, Manape Shogole, Amy L Slogrove, Nomakhawuta Moshani, Andrew Boulle, Jane Goudge, Frances Griffiths, Lee Fairlie, Ushma Mehta, Kerry Scott, Nirvana Pillay","doi":"10.1080/26410397.2023.2274667","DOIUrl":"10.1080/26410397.2023.2274667","url":null,"abstract":"<p><p>Despite the expanding digitisation of individual health data, informed consent for the collection and use of health data is seldom explicitly sought in public sector clinics in South Africa. This study aims to identify perceptions of informed consent practices for health data capture, access, and use in Gauteng and the Western Cape provinces of South Africa. Data collection from September to December 2021 included in-depth interviews with healthcare providers (<i>n</i> = 12) and women (<i>n</i> = 62) attending maternity services. Study findings suggest that most patients were not aware that their data were being used for purposes beyond the individualised provision of medical care. Understanding the concept of anonymised use of electronic health data was at times challenging for patients who understood their data in the limited context of paper-based folders and booklets. When asked about preferences for electronic data, patients overwhelmingly were in favour of digitisation. They viewed electronic access to their health data as facilitating rapid and continuous access to health information. Patients were additionally asked about preferences, including delivery of health information, onward health data use, and recontacting. Understanding of these use cases varied and was often challenging to convey to participants who understood their health data in the context of information inputted into their paper folders. Future systems need to be established to collect informed consent for onward health data use. In light of perceived ties to the care received, these systems need to ensure that patient preferences do not impede the content nor quality of care received.</p>","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 4","pages":"2274667"},"PeriodicalIF":3.3,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11001361/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138048103","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01DOI: 10.1080/26410397.2023.2220188
Joni Lariat, Chido Dziva Chikwari, Ethel Dauya, Valentine T Baumu, Victor Kaisi, Laura Kafata, Esnath Meza, Victoria Simms, Constance Mackworth-Young, Helena Rochford, Anna Machiha, Tsitsi Bandason, Suzanna C Francis, Rashida A Ferrand, Sarah Bernays
<p><p>Partner notification (PN) is considered integral to the management of sexually transmitted infections (STI). Patient-referral is a common PN strategy and relies on index cases notifying and encouraging their partners to access treatment; however, it has shown limited efficacy. We conducted a mixed methods study to understand young people's experiences of PN, particularly the risks and challenges encountered during patient-referral. All young people (16-24 years) attending a community-based sexual and reproductive health service in Zimbabwe who were diagnosed with an STI were counselled and offered PN slips, which enabled their partners to access free treatment at the service. PN slip uptake and partner treatment were recorded. Among 1807 young people (85.0% female) offered PN slips, 745 (41.2%) took up ≥1 PN slip and 103 partners (5.7%) returned for treatment. Most participants described feeling ill-equipped to counsel and persuade their partners to seek treatment. Between June and August 2021, youth researchers conducted in-depth interviews with 41 purposively selected young people diagnosed with an STI to explore their experiences of PN. PN posed considerable social risks, threatening their emotional and physical safety. Except for a minority in long-term, publicly acknowledged relationships, participants did not expect PN would achieve successful outcomes. Public health discourse, which constructs PN as "the right thing to do", influenced participants to adopt narratives that concealed the difficulties of PN and their unmet needs. Urgent interrogation is needed of whether PN is a suitable or constructive strategy to continue pursuing with young people. To improve the outcomes of preventing reinfection and onward transmission of STIs, we must consider developing alternative strategies that better align with young people's lived experiences.<b>Plain language summary</b> Partner notification is a public health strategy used to trace the sexual partners of people who have received a sexually transmitted infection (STI) diagnosis. It aims to interrupt the chains of STI transmission and prevent reinfection by treating both the person diagnosed and their sexual partners. The least effective but most common partner notification strategy used in many resource-limited settings is called "patient referral". This involves a sexual healthcare provider encouraging the person diagnosed to give a "partner notification slip" to their potentially exposed sexual partner/s and persuading them to access treatment. This research sought to better understand young people's experiences of partner notification, particularly the risks and challenges they faced during patient-referral.All young people (16-24 years) attending a community-based sexual and reproductive health service in Zimbabwe who were diagnosed with an STI were counselled and offered PN slips, which enabled their partners to access free treatment at the service. Young people trained as researchers
{"title":"<i>\"It's not safe for me and what would it achieve?\"</i> Acceptability of patient-referral partner notification for sexually transmitted infections to young people, a mixed methods study from Zimbabwe.","authors":"Joni Lariat, Chido Dziva Chikwari, Ethel Dauya, Valentine T Baumu, Victor Kaisi, Laura Kafata, Esnath Meza, Victoria Simms, Constance Mackworth-Young, Helena Rochford, Anna Machiha, Tsitsi Bandason, Suzanna C Francis, Rashida A Ferrand, Sarah Bernays","doi":"10.1080/26410397.2023.2220188","DOIUrl":"10.1080/26410397.2023.2220188","url":null,"abstract":"<p><p>Partner notification (PN) is considered integral to the management of sexually transmitted infections (STI). Patient-referral is a common PN strategy and relies on index cases notifying and encouraging their partners to access treatment; however, it has shown limited efficacy. We conducted a mixed methods study to understand young people's experiences of PN, particularly the risks and challenges encountered during patient-referral. All young people (16-24 years) attending a community-based sexual and reproductive health service in Zimbabwe who were diagnosed with an STI were counselled and offered PN slips, which enabled their partners to access free treatment at the service. PN slip uptake and partner treatment were recorded. Among 1807 young people (85.0% female) offered PN slips, 745 (41.2%) took up ≥1 PN slip and 103 partners (5.7%) returned for treatment. Most participants described feeling ill-equipped to counsel and persuade their partners to seek treatment. Between June and August 2021, youth researchers conducted in-depth interviews with 41 purposively selected young people diagnosed with an STI to explore their experiences of PN. PN posed considerable social risks, threatening their emotional and physical safety. Except for a minority in long-term, publicly acknowledged relationships, participants did not expect PN would achieve successful outcomes. Public health discourse, which constructs PN as \"the right thing to do\", influenced participants to adopt narratives that concealed the difficulties of PN and their unmet needs. Urgent interrogation is needed of whether PN is a suitable or constructive strategy to continue pursuing with young people. To improve the outcomes of preventing reinfection and onward transmission of STIs, we must consider developing alternative strategies that better align with young people's lived experiences.<b>Plain language summary</b> Partner notification is a public health strategy used to trace the sexual partners of people who have received a sexually transmitted infection (STI) diagnosis. It aims to interrupt the chains of STI transmission and prevent reinfection by treating both the person diagnosed and their sexual partners. The least effective but most common partner notification strategy used in many resource-limited settings is called \"patient referral\". This involves a sexual healthcare provider encouraging the person diagnosed to give a \"partner notification slip\" to their potentially exposed sexual partner/s and persuading them to access treatment. This research sought to better understand young people's experiences of partner notification, particularly the risks and challenges they faced during patient-referral.All young people (16-24 years) attending a community-based sexual and reproductive health service in Zimbabwe who were diagnosed with an STI were counselled and offered PN slips, which enabled their partners to access free treatment at the service. Young people trained as researchers ","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 1","pages":"2220188"},"PeriodicalIF":3.3,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e4/e6/ZRHM_31_2220188.PMC10424614.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10005445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2023-10-13DOI: 10.1080/26410397.2023.2260174
Katy Footman, Pippa Page, Victoria Boydell, Megan McLaren, Sandra Mudhune
The COVID-19 pandemic caused significant disruption to sexual and reproductive health and rights (SRHR) globally but there is little published evidence on the COVID-19 response of SRHR programmes, or lessons learned through their adaptations. To document the COVID-19 response of a global SRHR programme (the Women's Integrated Sexual Health programme), in-depth interviews were conducted between April and July 2021 with 22 key informants from implementing partners in Sierra Leone, Ethiopia and central or regional offices, the UK Foreign, Commonwealth and Development Office and the third-party monitoring partner. Framework analysis methods were used. Several rapid COVID-19 adaptations were identified: the development of crisis management and communication teams; increased partnership and engagement with government; reduced contact and risk in service delivery; reformulated community mobilisation; flexible performance management and remote methods of quality assurance; and sharing of learnings alongside the development of new guidance and tools. Throughout the pandemic, the programme was able to continue high-quality service delivery, though equity goals proved more difficult to reach. Challenges included the continually changing environment, competing pressures on governments, burdensome reporting, and staff burnout. The pandemic response was facilitated by prior experience of health emergencies, strong government relationships, a supportive workforce and some pre-existing approaches, tools, and systems. This study has identified important lessons that can inform programming in future crises, including the need for immediate recognition of SRHR as essential, sustained support for staff, use of multiple mechanisms to reach marginalised groups, adequate funding for equity goals, and a better balance between the burden of reporting and accountability needs.
{"title":"Adapting to a global pandemic: a qualitative assessment of programmatic responses to COVID-19 in the multi-country Women's Integrated Sexual Health (WISH) programme.","authors":"Katy Footman, Pippa Page, Victoria Boydell, Megan McLaren, Sandra Mudhune","doi":"10.1080/26410397.2023.2260174","DOIUrl":"10.1080/26410397.2023.2260174","url":null,"abstract":"<p><p>The COVID-19 pandemic caused significant disruption to sexual and reproductive health and rights (SRHR) globally but there is little published evidence on the COVID-19 response of SRHR programmes, or lessons learned through their adaptations. To document the COVID-19 response of a global SRHR programme (the Women's Integrated Sexual Health programme), in-depth interviews were conducted between April and July 2021 with 22 key informants from implementing partners in Sierra Leone, Ethiopia and central or regional offices, the UK Foreign, Commonwealth and Development Office and the third-party monitoring partner. Framework analysis methods were used. Several rapid COVID-19 adaptations were identified: the development of crisis management and communication teams; increased partnership and engagement with government; reduced contact and risk in service delivery; reformulated community mobilisation; flexible performance management and remote methods of quality assurance; and sharing of learnings alongside the development of new guidance and tools. Throughout the pandemic, the programme was able to continue high-quality service delivery, though equity goals proved more difficult to reach. Challenges included the continually changing environment, competing pressures on governments, burdensome reporting, and staff burnout. The pandemic response was facilitated by prior experience of health emergencies, strong government relationships, a supportive workforce and some pre-existing approaches, tools, and systems. This study has identified important lessons that can inform programming in future crises, including the need for immediate recognition of SRHR as essential, sustained support for staff, use of multiple mechanisms to reach marginalised groups, adequate funding for equity goals, and a better balance between the burden of reporting and accountability needs.</p>","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 1","pages":"2260174"},"PeriodicalIF":6.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578083/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41215093","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2023-10-04DOI: 10.1080/26410397.2023.2257073
Lilian Mutea, Justinah Maluni, Mark Kabue, Vincent Were, Susan Ontiri, Kristien Michielsen, Peter Gichangi
Adolescent sexual and reproductive health (ASRH) services are key to improving the health of adolescents. This study aimed to establish the effectiveness of an intervention that combined activities in health facilities and communities in Kenya to increase utilisation of ASRH services. A quasi-experimental evaluation design was used to assess the effectiveness of the intervention. Using a stratified cluster sampling approach, two cross-sectional household surveys targeting girls aged 15-19 were conducted at baseline (September 2019) and endline (December 2020) in intervention and comparison. We combined the difference-in-difference approach to analyse the net change in outcomes between intervention and comparison arms of the study at baseline and endline and coarsened exact matching for variables that were significantly different to address the imbalance. There were a total of 1011 participants in the intervention arm and 880 in the comparison arm. Descriptive results showed a net increase of 12.7% in intervention sites in the knowledge of misconceptions about sex, pregnancy, and contraception, compared to 10.4% in the control site. In the multivariate regression analysis, two outcomes remained significant: decreases in adolescents' discomfort when seeking ASRH services because of either fear of parents (aPR = 0.58, 95% CI = 0.42-0.79, P = 0.001) or a lack of support from their partner (aPR = 0.25, 95% CI = 0.08-0.82, P = 0.023). The intervention combining a facility and community approach was not effective in increasing the use of ASRH information and services. Possible reasons for this are explored.
{"title":"The effectiveness of combined approaches towards improving utilisation of adolescent sexual and reproductive health services in Kenya: a quasi-experimental evaluation.","authors":"Lilian Mutea, Justinah Maluni, Mark Kabue, Vincent Were, Susan Ontiri, Kristien Michielsen, Peter Gichangi","doi":"10.1080/26410397.2023.2257073","DOIUrl":"10.1080/26410397.2023.2257073","url":null,"abstract":"<p><p>Adolescent sexual and reproductive health (ASRH) services are key to improving the health of adolescents. This study aimed to establish the effectiveness of an intervention that combined activities in health facilities and communities in Kenya to increase utilisation of ASRH services. A quasi-experimental evaluation design was used to assess the effectiveness of the intervention. Using a stratified cluster sampling approach, two cross-sectional household surveys targeting girls aged 15-19 were conducted at baseline (September 2019) and endline (December 2020) in intervention and comparison. We combined the difference-in-difference approach to analyse the net change in outcomes between intervention and comparison arms of the study at baseline and endline and coarsened exact matching for variables that were significantly different to address the imbalance. There were a total of 1011 participants in the intervention arm and 880 in the comparison arm. Descriptive results showed a net increase of 12.7% in intervention sites in the knowledge of misconceptions about sex, pregnancy, and contraception, compared to 10.4% in the control site. In the multivariate regression analysis, two outcomes remained significant: decreases in adolescents' discomfort when seeking ASRH services because of either fear of parents (aPR = 0.58, 95% CI = 0.42-0.79, <i>P</i> = 0.001) or a lack of support from their partner (aPR = 0.25, 95% CI = 0.08-0.82, <i>P</i> = 0.023). The intervention combining a facility and community approach was not effective in increasing the use of ASRH information and services. Possible reasons for this are explored.</p>","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":"31 1","pages":"2257073"},"PeriodicalIF":6.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/9e/ef/ZRHM_31_2257073.PMC10552573.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41158344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2023-11-27DOI: 10.1080/26410397.2023.2275840
Janna Metzler, Aisha Hutchinson, Katrina Kiss
Globally, more than 12 million girls under the age of 18 are forced to marry every year. Progress on ending child marriage in the Arab region is slowing, and risks being reversed, due to an increase in conflict-affected populations and widespread economic crisis. The aim of this paper is to consider the research priorities across the region to inform effective and accelerated child marriage prevention and response programming within the Arab region. Seventy-three specialists supporting child marriage prevention and response programming in the Arab region engaged with up to three phases of an online Delphi consultation process on research gaps and the research environment between July 2019 and December 2021. Proposals of research gaps were elicited, reviewed, and rated by participants to confirm a shared learning agenda. Participants identified 50 different research gaps across 7 main areas, reaching a high level of consensus support for 23 of 50 statements. Clear consensus was reached in relation to an increased need to produce and use evidence to support programme development, and further research on specific drivers and consequences of child marriage. The least consensus was found in relation to how research can inform prevention and response efforts within the law and legal system. The results provide the foundation of a child marriage research agenda for the Arab region which takes into account regional distinctiveness and builds on the global momentum for child marriage research. Mechanisms are in place to do this through the Regional Action Forum, and other networks across the region.
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Pub Date : 2023-09-01DOI: 10.1080/26410397.2023.2245617
Jung Chen
This is an important book in the field of studying reproduction and health, and a timely response to the social changes following the policy shift that abolished the anonymity of gamete donors. Many scholars have been looking at relevant issues, mostly in relation to donor-recipient people, yet less attention has been paid to donors and their families. Petra Nordqvist and Leah Gilman examine gamete donors’ experiences from a relational perspective. Donors: Curious Connections in Donor Conception aims to explore the effects of changes in the legal, social, cultural, and technological context at this specific historical moment on people who have been or are considering becoming gamete (sperm or ovum) donors and how they make sense of the connections with the donorconceived children and the families. The shift from donor anonymity to traceability in the UK, which began in 2005, signifies a great transition from secrecy to openness in terms of the identity of people who donate sperm and ova. This regulatory change is the response to donorconceived people’s campaign for openness and the right for them to contact donors after they reach the age of 18 (p. 16). It has resulted in a new protocol for clinical practice in reproductive medicine and reflects wider sociocultural changes. By depicting donors’ lived experiences, Donors explains “the broader shift in donor conception practices and cultures” as the consent donor policy enacted and, at the same time, the emerging use of the Internet and social media to perform informal donation (p. 211). Thus, Donors examins both people who participate in donations in clinics, and those who donate informally, who are already acquainted with recipient parents. By looking at various donations, Donors captures how people perceive donation differently through investigating donors’ experiences as well as their relationships and their personal lives. With the expansion of reproductive gamete donation in the UK and worldwide, increasing research interests have been addressed around recipients, including recipient parents and donor-conceived children. However, there is a shortage of scholarly literature on the donor families and their relationships, especially research conducted via qualitative approaches, which can give a more in-depth understanding of how donation decisions shape donors’ lives and those with whom they share connections. Methodologically, Petra Nordqvist and Leah Gilman explore gamete donors’ experiences from a relational perspective and employ the personal life approach in sociology, to explore how social policies impact on people’s perceptions of connectedness. Donors sees gamete donation as a reflection of practices and relatedness negotiations, as well as a response to shifting social and political agendas. In the Introduction, the authors begin with the story of a sperm donor, Zak, to bring out the pressing questions: What does it mean to be a donor? (p. 1) How does that affect the donor, and their f
{"title":"Donors: curious connections in donor conception","authors":"Jung Chen","doi":"10.1080/26410397.2023.2245617","DOIUrl":"https://doi.org/10.1080/26410397.2023.2245617","url":null,"abstract":"This is an important book in the field of studying reproduction and health, and a timely response to the social changes following the policy shift that abolished the anonymity of gamete donors. Many scholars have been looking at relevant issues, mostly in relation to donor-recipient people, yet less attention has been paid to donors and their families. Petra Nordqvist and Leah Gilman examine gamete donors’ experiences from a relational perspective. Donors: Curious Connections in Donor Conception aims to explore the effects of changes in the legal, social, cultural, and technological context at this specific historical moment on people who have been or are considering becoming gamete (sperm or ovum) donors and how they make sense of the connections with the donorconceived children and the families. The shift from donor anonymity to traceability in the UK, which began in 2005, signifies a great transition from secrecy to openness in terms of the identity of people who donate sperm and ova. This regulatory change is the response to donorconceived people’s campaign for openness and the right for them to contact donors after they reach the age of 18 (p. 16). It has resulted in a new protocol for clinical practice in reproductive medicine and reflects wider sociocultural changes. By depicting donors’ lived experiences, Donors explains “the broader shift in donor conception practices and cultures” as the consent donor policy enacted and, at the same time, the emerging use of the Internet and social media to perform informal donation (p. 211). Thus, Donors examins both people who participate in donations in clinics, and those who donate informally, who are already acquainted with recipient parents. By looking at various donations, Donors captures how people perceive donation differently through investigating donors’ experiences as well as their relationships and their personal lives. With the expansion of reproductive gamete donation in the UK and worldwide, increasing research interests have been addressed around recipients, including recipient parents and donor-conceived children. However, there is a shortage of scholarly literature on the donor families and their relationships, especially research conducted via qualitative approaches, which can give a more in-depth understanding of how donation decisions shape donors’ lives and those with whom they share connections. Methodologically, Petra Nordqvist and Leah Gilman explore gamete donors’ experiences from a relational perspective and employ the personal life approach in sociology, to explore how social policies impact on people’s perceptions of connectedness. Donors sees gamete donation as a reflection of practices and relatedness negotiations, as well as a response to shifting social and political agendas. In the Introduction, the authors begin with the story of a sperm donor, Zak, to bring out the pressing questions: What does it mean to be a donor? (p. 1) How does that affect the donor, and their f","PeriodicalId":37074,"journal":{"name":"Sexual and Reproductive Health Matters","volume":" ","pages":""},"PeriodicalIF":6.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46003655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}