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- Publisher Website: 10.1016/j.bpobgyn.2024.102541
- Scopus: eid_2-s2.0-85203531222
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Article: Intimate partner violence during pregnancy: To screen or not to screen?
Title | Intimate partner violence during pregnancy: To screen or not to screen? |
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Authors | |
Keywords | Academia-community-industrial partnerships Intimate partner violence Maternal outcomes Postnatal depression Universal screening |
Issue Date | 1-Dec-2024 |
Publisher | Elsevier |
Citation | Best Practice and Research: Clinical Obstetrics and Gynaecology, 2024, v. 97 How to Cite? |
Abstract | Intimate partner violence (IPV) during pregnancy emerges as a compelling and urgent concern within the domain of public health, casting a long shadow over a substantial cohort of women. Its pernicious consequences extend beyond the individual, enveloping the well-being of both the mother and the fetus, giving rise to an elevated risk of preterm birth, low birth weight, fetal harm, and maternal psychological distress, including depression, anxiety, post-traumatic stress disorder, and, tragically, maternal mortality. Despite the prevalence of IPV being comparable to other conditions like gestational diabetes and preeclampsia, a universal screening protocol for IPV remains absent globally. We reviewed the clinical guidelines and practices concerning IPV screening, painstakingly scrutinizing their contextual nuances across diverse nations. Our study unveils multifaceted challenges of implementing universal screening. These hurdles encompass impediments to victim awareness and disclosure, limitations in healthcare providers' knowledge and training, and the formidable structural barriers entrenched within healthcare systems. Concurrently, we delve into the potential biomarkers intricately entwined with IPV. These promising markers encompass inflammatory indicators, epigenetic and genetic influences, and a diverse array of chemical compounds and proteins. Lastly, we discussed various criteria for universal screening including (1) valid and reliable screening tool; (2) target population as pregnant women; (3) scientific evidence of screening programme; and (4) integration of education, testing, clinical services, and programme management to minimise the challenges, which are paramount. With the advancement of digital technology and various biomarkers identification, screening and detecting IPV in clinical settings can be conducted systemically. A systems-level interventions with academia-community-indutrial partnerships can help connect pregnant women to desire support services to avoid adverse maternal and child health outcomes. |
Persistent Identifier | http://hdl.handle.net/10722/350206 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.532 |
DC Field | Value | Language |
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dc.contributor.author | Wong Janet Yuen-Ha | - |
dc.contributor.author | Zhu, Shiben | - |
dc.contributor.author | Ma, Haixia | - |
dc.contributor.author | Ip Patrick | - |
dc.contributor.author | Chan, Ko Ling | - |
dc.contributor.author | Leung Wing Cheong | - |
dc.date.accessioned | 2024-10-21T03:56:51Z | - |
dc.date.available | 2024-10-21T03:56:51Z | - |
dc.date.issued | 2024-12-01 | - |
dc.identifier.citation | Best Practice and Research: Clinical Obstetrics and Gynaecology, 2024, v. 97 | - |
dc.identifier.issn | 1521-6934 | - |
dc.identifier.uri | http://hdl.handle.net/10722/350206 | - |
dc.description.abstract | <p>Intimate partner violence (IPV) during pregnancy emerges as a compelling and urgent concern within the domain of public health, casting a long shadow over a substantial cohort of women. Its pernicious consequences extend beyond the individual, enveloping the well-being of both the mother and the fetus, giving rise to an elevated risk of preterm birth, low birth weight, fetal harm, and maternal psychological distress, including depression, anxiety, post-traumatic stress disorder, and, tragically, maternal mortality. Despite the prevalence of IPV being comparable to other conditions like gestational diabetes and preeclampsia, a universal screening protocol for IPV remains absent globally. We reviewed the clinical guidelines and practices concerning IPV screening, painstakingly scrutinizing their contextual nuances across diverse nations. Our study unveils multifaceted challenges of implementing universal screening. These hurdles encompass impediments to victim awareness and disclosure, limitations in healthcare providers' knowledge and training, and the formidable structural barriers entrenched within healthcare systems. Concurrently, we delve into the potential biomarkers intricately entwined with IPV. These promising markers encompass inflammatory indicators, epigenetic and genetic influences, and a diverse array of chemical compounds and proteins. Lastly, we discussed various criteria for universal screening including (1) valid and reliable screening tool; (2) target population as pregnant women; (3) scientific evidence of screening programme; and (4) integration of education, testing, clinical services, and programme management to minimise the challenges, which are paramount. With the advancement of digital technology and various biomarkers identification, screening and detecting IPV in clinical settings can be conducted systemically. A systems-level interventions with academia-community-indutrial partnerships can help connect pregnant women to desire support services to avoid adverse maternal and child health outcomes.</p> | - |
dc.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Best Practice and Research: Clinical Obstetrics and Gynaecology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Academia-community-industrial partnerships | - |
dc.subject | Intimate partner violence | - |
dc.subject | Maternal outcomes | - |
dc.subject | Postnatal depression | - |
dc.subject | Universal screening | - |
dc.title | Intimate partner violence during pregnancy: To screen or not to screen? | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.bpobgyn.2024.102541 | - |
dc.identifier.scopus | eid_2-s2.0-85203531222 | - |
dc.identifier.volume | 97 | - |
dc.identifier.issnl | 1521-6934 | - |