American Society of Hirudotherapy

Mechanical heart valve thrombosis during pregnancy under nonwarfarin anticoagulation therapy: Twocase report and literature review.

Case report published in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences (2021)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Case reportClinical TrialsDrug DevelopmentHuang et al. · Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 2021

Abstract

Anticoagulation drugs should be used for patients with mechanical heart valve (MHV) in case of potential risk of thrombosis. Pregnant women with MHV have to change therapies due to teratogenic effect of some anti-coagulation drugs. European Society of Cardiology clinical guidelines for the management of cardiovascular diseases during pregnancy gives specific suggestions for anticoagulation therapy.We have treated 2 patients with mechanical heart valve thrombosis (MVT) during pregnancy: One received low molecular weight heparin (LMWH) throughout the pregnancy and developed MVT at the third trimester of pregnancy; one developed MVT at the first trimester when replacing vitamin K antagonists (VKA) with LMWH. These patients raised secondary reflection on the balance between clinical guideline and personalized medicine. During LMWH therapy, we should dynamically monitor patients' anti-activated factor X (anti-Xa) level to evaluate coagulation function during pregnancy. When a pregnant woman with MHV develops symptoms of acute heart failure, stuck mechanical valve should be paid attention to and surgery should be promptly performed if necessary. 有二尖瓣机械瓣置换史的患者必须规律服用抗凝药物以抵抗血栓风险,华法林等抗凝药物因存在致畸风险,故孕妇在妊娠过程中必须更换抗凝方案。欧洲心血管学会临床指南对妊娠期间抗凝治疗给出了明确的建议。笔者报告2例患者:1例妊娠期全程用肝素抗凝,导致妊娠晚期血栓卡瓣;1例遵循指南,在早孕期使用肝素替代抗凝治疗亦出现血栓卡瓣。针对指南和个体化用药之间的平衡,笔者提出如下建议:换瓣患者妊娠期的抗凝必须在严密监测凝血功能的情况下采取个体化的方案;当这类孕妇出现急性心力衰竭症状时,需要排除机械瓣卡瓣的情况,并积极行手术处理。. 有二尖瓣机械瓣置换史的患者必须规律服用抗凝药物以抵抗血栓风险,华法林等抗凝药物因存在致畸风险,故孕妇在妊娠过程中必须更换抗凝方案。欧洲心血管学会临床指南对妊娠期间抗凝治疗给出了明确的建议。笔者报告2例患者:1例妊娠期全程用肝素抗凝,导致妊娠晚期血栓卡瓣;1例遵循指南,在早孕期使用肝素替代抗凝治疗亦出现血栓卡瓣。针对指南和个体化用药之间的平衡,笔者提出如下建议:换瓣患者妊娠期的抗凝必须在严密监测凝血功能的情况下采取个体化的方案;当这类孕妇出现急性心力衰竭症状时,需要排除机械瓣卡瓣的情况,并积极行手术处理。

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeCase ReportsJournal ArticleReview
Indexed MeSH termsAnticoagulantsFemaleHeart Valve ProsthesisHeart ValvesHeparin, Low-Molecular-WeightHumansPregnancyPregnancy Complications, CardiovascularThrombosis

Summary

Anticoagulation drugs should be used for patients with mechanical heart valve (MHV) in case of potential risk of thrombosis. Pregnant women with MHV have to change therapies due to teratogenic effect of some anti-coagulation drugs.

Why This Matters for Hirudotherapy

This article reports two cases of pregnant women with mechanical heart valve thrombosis—one who received low-molecular-weight heparin throughout pregnancy and developed thrombosis in the third trimester, and another who developed thrombosis during vitamin K antagonist-to-LMWH transition in the first trimester—and offers clinical reflections on anticoagulation monitoring and individualized therapy. The abstract makes no mention of leeches, hirudin, hirudotherapy, or any leech-derived substances. The study is focused entirely on modern pharmacological anticoagulation and mechanical valve management in pregnancy, with no demonstrated connection to therapeutic leeching or the leech secretome.

Citation

Mechanical heart valve thrombosis during pregnancy under nonwarfarin anticoagulation therapy: Twocase report and literature review.

Huang et al. · Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 2021

Added to ASH library: May 28, 2026 · Site last updated: June 18, 2026

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.