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Estimated prevalence of sickle cell in northern Haiti.

机译:海地北部镰状细胞的估计患病率。

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摘要

OBJECTIVE: The purpose of this study is to estimate the prevalence of sickle hemoglobin in northern Haiti. DESIGN: Sickle cell testing occurred from 2002-2009. Blood samples from 1035 subjects were collected for diagnostic purposes, de-identified, and made available for the study. SETTING: Bethesda Medical Center and Eben-Ezer Clinic in northern Haiti. SUBJECTS: Study subjects included prenatal patients, their companions, clinic staff and volunteers. All subjects were Haitian and selected to most closely represent healthy patients present at the clinic. Deidentification of the blood samples precluded the need for informed consent. MAIN OUTCOME MEASURES: Each subject was tested for sickle hemoglobin using a standard hemoglobin solubility test and results were recorded as either positive or negative. RESULTS: The estimated prevalence of sickle hemoglobin was 15.1% with a 95% confidence interval of 12.2-18%. CONCLUSIONS: These prevalence rates validate the clinical significance of sickle cell disorder, help guide clinical decisions, and suggest the need to develop intervention programs among the people of northern Haiti.
机译:目的:本研究的目的是评估海地北部镰状血红蛋白的患病率。设计:镰状细胞测试发生于2002-2009年。收集了1035名受试者的血样用于诊断目的,对其进行了身份识别,然后用于研究。地点:海地北部的贝塞斯达医疗中心和埃本-埃泽诊所。受试者:研究对象包括产前患者,其同伴,诊所工作人员和志愿者。所有受试者均为海地人,并被选为最能代表临床患者的健康患者。血液样品的身份鉴定排除了获得知情同意的必要。主要观察指标:使用标准血红蛋白溶解度测试对每位受试者的镰刀血红蛋白进行测试,结果记录为阳性或阴性。结果:镰状血红蛋白的估计患病率为15.1%,95%的置信区间为12.2-18%。结论:这些患病率证实了镰状细胞疾病的临床意义,有助于指导临床决策,并表明有必要在海地北部人民中制定干预计划。

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