Clinical characteristics and management outcomes of patients with hydatidiform mole in a national referral hospital in Kenya: A retrospective study

Cyprian Nyariki, Rose Kosgei
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 Objective: To determine patient clinical characteristics and management outcomes of hydatidiform mole diagnosed at Kenyatta National Hospital, Nairobi, Kenya.
 Methods: A descriptive retrospective study design was employed. The medical records of patients admitted with a clinical diagnosis of hydatidiform mole at the Kenyatta National Hospital between January 2013 and December 2017 were retrieved. Data were collected using an abstraction tool, entered, and analyzed using the Statistical Package for Social Sciences (SPSS) version 22 (IBM, Armonk, NY, USA). Categorical data were summarized into frequencies and proportions and continuous data into means, standard deviations, medians, and interquartile ranges.
 Results: During the study period, 137 records of patients admitted and managed for hydatidiform mole were retrieved. Most, 110 (80%) and 97 (71%) patients were 20-34 years old and multiparous, respectively. The mean gestational age at presentation was 17 weeks (SD 7.4), and bleeding was the most common symptom in 105 (77%) patients. Only 46 (34%) patients had documented histological confirmation of the hydatidiform mole. None of the patients completed six months of follow-up; hence, there was no documentation of treatment outcomes.
 Conclusion: In this study, the clinical presentation of the hydatidiform mole was relatively uniform, but the approach to definitive diagnosis, management, and follow-up was suboptimal and inadequately documented. Hence, management outcomes cannot be objectively determined.","PeriodicalId":85009,"journal":{"name":"Journal of obstetrics & gynaecology of Eastern and Central Africa","volume":"78 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of obstetrics & gynaecology of Eastern and Central Africa","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59692/jogeca.v35i3.55","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Background: Hydatidiform mole is a benign form of gestational trophoblastic disease with potential for malignant transformation. It is characterized by abnormal trophoblastic proliferation with placental villi vascular welling with or without embryo formation. Objective: To determine patient clinical characteristics and management outcomes of hydatidiform mole diagnosed at Kenyatta National Hospital, Nairobi, Kenya. Methods: A descriptive retrospective study design was employed. The medical records of patients admitted with a clinical diagnosis of hydatidiform mole at the Kenyatta National Hospital between January 2013 and December 2017 were retrieved. Data were collected using an abstraction tool, entered, and analyzed using the Statistical Package for Social Sciences (SPSS) version 22 (IBM, Armonk, NY, USA). Categorical data were summarized into frequencies and proportions and continuous data into means, standard deviations, medians, and interquartile ranges. Results: During the study period, 137 records of patients admitted and managed for hydatidiform mole were retrieved. Most, 110 (80%) and 97 (71%) patients were 20-34 years old and multiparous, respectively. The mean gestational age at presentation was 17 weeks (SD 7.4), and bleeding was the most common symptom in 105 (77%) patients. Only 46 (34%) patients had documented histological confirmation of the hydatidiform mole. None of the patients completed six months of follow-up; hence, there was no documentation of treatment outcomes. Conclusion: In this study, the clinical presentation of the hydatidiform mole was relatively uniform, but the approach to definitive diagnosis, management, and follow-up was suboptimal and inadequately documented. Hence, management outcomes cannot be objectively determined.
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肯尼亚一家国家转诊医院包体痣患者的临床特征和治疗结果:一项回顾性研究
背景:葡萄胎是妊娠滋养细胞疾病的一种良性形式,有恶性转化的可能。其特征是滋养细胞增生异常,胎盘绒毛血管增生,伴或不伴胚胎形成。 目的:了解肯尼亚内罗毕肯雅塔国家医院诊断的包体痣患者的临床特征和治疗结果。方法:采用描述性回顾性研究设计。检索了2013年1月至2017年12月在肯雅塔国立医院因临床诊断为葡萄胎而入院的患者的医疗记录。使用抽象工具收集数据,使用社会科学统计软件包(SPSS)第22版(IBM, Armonk, NY, USA)进行输入和分析。分类数据归纳为频率和比例,连续数据归纳为均值、标准差、中位数和四分位间距。 结果:在研究期间,检索了137例因葡萄胎入院和治疗的患者的记录。其中,20 ~ 34岁为110例(80%),产褥期为97例(71%)。分娩时的平均胎龄为17周(SD 7.4), 105例(77%)患者最常见的症状是出血。只有46例(34%)患者有组织学证实为葡萄胎。没有患者完成6个月的随访;因此,没有治疗结果的记录。 结论:在本研究中,葡萄胎的临床表现相对统一,但明确诊断、治疗和随访的方法不理想,文献记录不充分。因此,管理结果无法客观确定。
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