Obstetric Medicine最新文献

Stiff person syndrome and type 1 diabetes in pregnancy. 妊娠期僵硬综合征和1型糖尿病。

IF 0.5

Obstetric Medicine Pub Date : 2025-10-08 DOI: 10.1177/1753495X251378590

Kavita Narula, Victoria Singh Curry, Kerry Munro, Mandish K Dhanjal, Charlotte Frise

引用次数: 0

Gitelman's and Bartter's syndromes in pregnancy - a systematic review. 妊娠期吉特尔曼综合征和巴特综合征——系统回顾。

IF 0.5

Obstetric Medicine Pub Date : 2025-10-08 DOI: 10.1177/1753495X251380057

Andrew It Hebbard, Kathy Paizis, Briony A Cutts

{"title":"Gitelman's and Bartter's syndromes in pregnancy - a systematic review.","authors":"Andrew It Hebbard, Kathy Paizis, Briony A Cutts","doi":"10.1177/1753495X251380057","DOIUrl":"10.1177/1753495X251380057","url":null,"abstract":"Background: : Gitelman's syndrome (GS) and Bartter's syndrome (BS) are rare renal disorders causing electrolyte disturbances, with physiological changes of pregnancy potentially worsening symptoms and electrolyte derangement.Methods: A literature search of electronic databases was conducted using terms describing (1) GS or BS and (2) pregnancy, and the quality of studies was graded using the NIH/NHLBI quality assessment tool. Data collected included measures of maternal and neonatal outcomes, pregnancy information, and details of treatment, diagnosis, and electrolyte monitoring.Results: Fifty-eight pregnancies in 52 women were reported in GS, and 55 pregnancies in 27 women were reported in BS. Adverse events and symptoms, including intrauterine growth restriction, oligohydramnios, preterm birth, fatigue, weakness, and paraesthesia, were commonly reported. The mainstay of therapy remains oral and intravenous electrolyte replacement coupled with frequent monitoring.Conclusions: The management of GS and BS in pregnancy presents a challenge and has the potential for significant maternal and neonatal morbidity.","PeriodicalId":51717,"journal":{"name":"Obstetric Medicine","volume":" ","pages":"1753495X251380057"},"PeriodicalIF":0.5,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12507792/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145281642","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

Typhoid fever in pregnancy - a South Australian perspective. 怀孕期间的伤寒——南澳大利亚的观点。

IF 0.5

Obstetric Medicine Pub Date : 2025-09-30 DOI: 10.1177/1753495X251367098

Madalina Oprea, Jessica Gehlert

引用次数: 0

A case of antisynthetase syndrome with interstitial lung disease in pregnancy. 妊娠期抗合成酶综合征合并间质性肺疾病1例。

IF 0.5

Obstetric Medicine Pub Date : 2025-09-25 DOI: 10.1177/1753495X251380063

Esther Park, Kerry Munro, Melissa Wickremasinghe, Charlotte Jane Frise

引用次数: 0

'Ayurveda', hyperemesis and anaemia in pregnancy. 阿育吠陀，妊娠期呕吐和贫血。

IF 0.5

Obstetric Medicine Pub Date : 2025-09-16 DOI: 10.1177/1753495X251378589

Adam Morton

引用次数: 0

Ophthalmic conditions affecting the choroid and retina in pregnancy: An overview of key pathologies. 妊娠期影响脉络膜和视网膜的眼部疾病：主要病理综述。

IF 0.5

Obstetric Medicine Pub Date : 2025-09-10 DOI: 10.1177/1753495X251367092

Evita E Christou, Ariel Yuhan Ong, Christine A Kiire, Naomi Primrose, William R Tucker, Charlotte Frise, Samantha R de Silva

引用次数: 0

Clinical course and pregnancy outcomes in women with hereditary spherocytosis: Insights from a case series. 遗传性球形红细胞增多症妇女的临床过程和妊娠结局：来自一个病例系列的见解。

IF 0.5

Obstetric Medicine Pub Date : 2025-08-26 DOI: 10.1177/1753495X251367094

Bhabani Pegu, Panneerselvam Sivaranjani, Murali Subbaiah, Ambalakkuthan Murugesan

{"title":"Clinical course and pregnancy outcomes in women with hereditary spherocytosis: Insights from a case series.","authors":"Bhabani Pegu, Panneerselvam Sivaranjani, Murali Subbaiah, Ambalakkuthan Murugesan","doi":"10.1177/1753495X251367094","DOIUrl":"https://doi.org/10.1177/1753495X251367094","url":null,"abstract":"Background: Hereditary spherocytosis (HS) is a genetic haemolytic anaemia, mainly inherited in an autosomal dominant manner. Management varies by severity, and limited data exist on HS in pregnancy in India; this study assesses clinical and obstetric outcomes in affected women.Methods: This retrospective study at JIPMER from 2014 to 2020 included 10 pregnant women with confirmed HS identified from labour room records. Data on demographics, medical and obstetric history, clinical presentation, pregnancy course, delivery details, complications, maternal and neonatal intensive care unit admissions, laboratory findings and postpartum outcomes were collected using a structured proforma.Results: This case series of 10 pregnant women with HS highlights anaemia, jaundice, and weakness as common symptoms confirmed by laboratory findings. Most had term vaginal deliveries; one required caesarean section due to complications. Neonatal outcomes were favourable, with no neonatal HS cases. Anaemia was more pronounced in women without splenectomy, while splenectomised patients showed greater hematologic stability. Bone marrow findings indicated compensatory erythroid hyperplasia. Diagnosis relied on clinical and haematological criteria, as genetic testing was not performed.Conclusion: HS in pregnancy is rare but manageable with appropriate antenatal care. This study confirms its classical presentation in the Indian population and supports early diagnosis, Eosin-5-maleimide testing and supportive management. Genetic testing and improved postnatal surveillance are recommended.","PeriodicalId":51717,"journal":{"name":"Obstetric Medicine","volume":" ","pages":"1753495X251367094"},"PeriodicalIF":0.5,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12380719/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144977927","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

Septic arthritis of the pubic symphysis, a rare cause of peripartum pelvic pain: A case report. 脓毒性耻骨联合关节炎，一个罕见的原因围产期盆腔疼痛：1例报告。

IF 0.5

Obstetric Medicine Pub Date : 2025-08-25 DOI: 10.1177/1753495X251370021

Lesley Thellend, Dayne Ortved

{"title":"Septic arthritis of the pubic symphysis, a rare cause of peripartum pelvic pain: A case report.","authors":"Lesley Thellend, Dayne Ortved","doi":"10.1177/1753495X251370021","DOIUrl":"https://doi.org/10.1177/1753495X251370021","url":null,"abstract":"Septic arthritis of the pubic symphysis is a rare but potentially life-threatening condition, particularly in the peripartum period. This case report details a 32-year-old woman in her first pregnancy, who developed severe pelvic pain, fever, and immobility following induction of labor at 41 weeks and 2 days of gestation. Initially diagnosed with chorioamnionitis, the patient underwent a caesarean section, but persistent groin pain and elevated inflammatory markers led to the discovery of septic arthritis of the pubic symphysis, confirmed by computed tomography and magnetic resonance imaging. Blood cultures grew methicillin-sensitive Staphylococcus aureus. The patient was treated with a 6-week course of intravenous cefazolin, and her condition complicated by endocarditis. Despite the severity of her illness, she made a full recovery and went on to have a successful subsequent pregnancy. This case emphasizes the importance of considering septic arthritis in peripartum pelvic pain, as early detection and treatment can prevent severe complications and preserve functional recovery.","PeriodicalId":51717,"journal":{"name":"Obstetric Medicine","volume":" ","pages":"1753495X251370021"},"PeriodicalIF":0.5,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12378115/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144977951","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

Management of hairy cell leukaemia in pregnancy. 妊娠期毛细胞白血病的处理。

IF 0.5

Obstetric Medicine Pub Date : 2025-08-19 DOI: 10.1177/1753495X251356377

Simone Da Cruz, Kylie Mason, William Renwick, Joanne M Said, Briony A Cutts

{"title":"Management of hairy cell leukaemia in pregnancy.","authors":"Simone Da Cruz, Kylie Mason, William Renwick, Joanne M Said, Briony A Cutts","doi":"10.1177/1753495X251356377","DOIUrl":"https://doi.org/10.1177/1753495X251356377","url":null,"abstract":"Background: Hairy cell leukaemia (HCL) represents less 1% of all lymphoid neoplasms with cases rarely reported in pregnancy. Management of HCL requires multidisciplinary care to optimise maternal and neonatal outcomes.Methods: A literature search of Ovid MEDLINE and EMBASE for 'hairy cell leukaemia' and 'Pregnancy' was undertaken.Results: Thirteen cases were reviewed including three within our own institutions. Interferon-alpha was the most prominent treatment at varying doses in n = 3 (23%) patients. Other management included antenatal cladribine and rituximab, post-partum cladribine with and without rituximab, laparoscopic splenectomy and termination of pregnancy. 46.1% (n = 6) of patients birthed vaginally. Due to thrombocytopenia, there was a greater proportion of caesarean delivery under general anaesthetic and half of the cases documented bleeding complications.Conclusion: Diagnosis and management of HCL in pregnancy is difficult. Women can be managed safely and outcome aims should be the same as non-pregnant patients.","PeriodicalId":51717,"journal":{"name":"Obstetric Medicine","volume":" ","pages":"1753495X251356377"},"PeriodicalIF":0.5,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12367712/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144978010","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

CYP24A1 loss-of-function mutation as a rare cause of parathyroid (PTH)-independent severe hypercalcaemia in pregnancy. CYP24A1功能缺失突变是妊娠期甲状旁腺（PTH）非依赖性严重高钙血症的罕见病因。

IF 0.5

Obstetric Medicine Pub Date : 2025-08-04 DOI: 10.1177/1753495X251349953

Adam Morton

引用次数: 0