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重度妊娠剧吐后韦尼克脑病:及时补充硫胺素的错失良机。

Wernicke Encephalopathy Following Severe Hyperemesis Gravidarum: A Missed Opportunity for Timely Thiamine Replacement.

作者信息

Mohamed Mustafa Risq Atiqah Munirah, Abd Aziz Noor Azah, Abdul Rahman Ahmad Fithri Azam

机构信息

Department of Family Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Kuala Lumpur, MYS.

Family Medicine, Klinik Kesihatan Ayer Keroh, Malacca City, MYS.

出版信息

Cureus. 2025 Jul 7;17(7):e87478. doi: 10.7759/cureus.87478. eCollection 2025 Jul.

Abstract

Wernicke's encephalopathy (WE) is a rare but potentially fatal complication of hyperemesis gravidarum (HG) caused by thiamine (vitamin B1) deficiency. WE is a medical emergency with complete recovery occurring in only a few cases associated with HG in pregnancy. Classical clinical features include the triad of ophthalmoplegia, altered mental status, and ataxia.  We report a case of a 42-year-old gravida 2 para 1 female patient at 16 weeks and 3-day period of gestation (POG) who presented to primary care during routine antenatal follow-up with a two-week history of sudden visual loss. She had experienced persistent nausea and vomiting for approximately eight weeks and reported a total weight loss of 15 kg since early pregnancy, including 5 kg in the past two weeks. At presentation, she appeared cachectic and extremely lethargic. She was tachycardic with a heart rate (HR) of 116 beats per minute, though her blood pressure remained normotensive. Eye examination revealed visual acuity of counting fingers with positive horizontal nystagmus, suggesting ophthalmoplegia. Fundoscopy was normal. Urinalysis showed ketonuria and proteinuria, with laboratory findings showing severe acute kidney injury (AKI). She was promptly referred to a tertiary center where she was treated with intravenous thiamine 500mg three times daily along with electrolyte replacement and hydration. Her symptoms improved rapidly, and her visual acuity returned to 6/6 bilaterally within 48 hours. She was discharged on a tapering dose of oral thiamine, which was to be continued until delivery, and remained well throughout the rest of her pregnancy. At 28 weeks' gestation, she underwent an emergency caesarean section due to fetal distress and delivered a premature baby girl weighing 1.3 kg. This case highlights the need for early recognition of WE in pregnant women with severe HG. Although rare, it is a reversible complication. Timely thiamine supplementation is essential for both treatment and prevention, and prophylaxis should be considered in high-risk patients.

摘要

韦尼克脑病(WE)是妊娠剧吐(HG)罕见但可能致命的并发症,由硫胺素(维生素B1)缺乏引起。WE是一种医疗急症,妊娠合并HG的病例中仅有少数能完全康复。典型的临床特征包括眼肌麻痹、精神状态改变和共济失调三联征。我们报告一例42岁、孕2产1的女性患者,妊娠16周零3天,在常规产前检查时因突发视力丧失两周前来初级保健机构就诊。她持续恶心和呕吐约八周,自妊娠早期以来体重减轻了15千克,其中过去两周减轻了5千克。就诊时,她消瘦且极度嗜睡。心率116次/分钟,心动过速,血压正常。眼部检查显示视力为指测,水平眼震阳性,提示眼肌麻痹。眼底检查正常。尿液分析显示酮尿和蛋白尿,实验室检查结果显示严重急性肾损伤(AKI)。她被迅速转诊至三级中心,在那里接受每日三次静脉注射500毫克硫胺素治疗,同时进行电解质补充和补液。她的症状迅速改善,48小时内双眼视力恢复到6/6。出院时给予逐渐减量的口服硫胺素,持续至分娩,在妊娠剩余时间里情况良好。妊娠28周时,因胎儿窘迫行急诊剖宫产,产下一名体重1.3千克的早产女婴。该病例强调了对患有严重HG的孕妇早期识别WE的必要性。虽然罕见,但这是一种可逆转的并发症。及时补充硫胺素对治疗和预防都至关重要,高危患者应考虑进行预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4fa/12328038/71c887573033/cureus-0017-00000087478-i01.jpg

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