首页> 外文期刊>Obstetrics and Gynecology: Journal of the American College of Obstetricians and Gynecologists >Accuracy of self-screening for contraindications to combined oral contraceptive use.
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Accuracy of self-screening for contraindications to combined oral contraceptive use.

机译:对口服避孕药联合使用的禁忌症进行自我筛查的准确性。

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OBJECTIVE: To estimate how well a convenience sample of women from the general population could self-screen for contraindications to combined oral contraceptives using a medical checklist. METHODS: Women 18-49 years old (N=1,271) were recruited at two shopping malls and a flea market in El Paso, Texas, and asked first whether they thought birth control pills were medically safe for them. They then used a checklist to determine the presence of level 3 or 4 contraindications to combined oral contraceptives according to the World Health Organization Medical Eligibility Criteria. The women then were interviewed by a blinded nurse practitioner, who also measured blood pressure. RESULTS: The sensitivity of the unaided self-screen to detect true contraindications was 56.2% (95% confidence interval [CI] 51.7-60.6%), and specificity was 57.6% (95% CI 54.0-61.1%). The sensitivity of the checklist to detect true contraindications was 83.2% (95% CI 79.5-86.3%), and specificity was 88.8% (95% CI 86.3-90.9%). Using the checklist, 6.6% (95% CI 5.2-8.0%) of women incorrectly thought they were eligible for use when, in fact, they were contraindicated, largely because of unrecognized hypertension. Seven percent (95% CI 5.4-8.2%) of women incorrectly thought they were contraindicated when they truly were not, primarily because of misclassification of migraine headaches. In regression analysis, younger women, more educated women, and Spanish speakers were significantly more likely to correctly self-screen (P<.05). CONCLUSION: Self-screening for contraindications to oral contraceptives using a medical checklist is relatively accurate. Unaided screening is inaccurate and reflects common misperceptions about the safety of oral contraceptives. Over-the-counter provision of this method likely would be safe, especially for younger women and if independent blood pressure screening were encouraged.
机译:目的:评估普通人群中方便妇女样本使用医学检查表自我筛选联合口服避孕药的禁忌症的程度。方法:在德克萨斯州埃尔帕索的两个购物中心和一个跳蚤市场招募了18-49岁的女性(N = 1,271),他们首先询问她们是否认为避孕药对他们而言是医学上安全的。然后,他们根据世界卫生组织的《医疗资格标准》,使用检查表确定联合口服避孕药的3级或4级禁忌症的存在。然后,一名不知情的护士从业人员采访了这些妇女,后者还测量了血压。结果:独立的自我筛查发现真正禁忌症的敏感性为56.2%(95%置信区间[CI] 51.7-60.6%),特异性为57.6%(95%CI 54.0-61.1%)。该检查表检测到真正禁忌症的敏感性为83.2%(95%CI 79.5-86.3%),特异性为88.8%(95%CI 86.3-90.9%)。使用检查表,实际上有禁忌症的妇女中有6.6%(95%CI 5.2-8.0%)错误地认为自己有使用资格,这在很大程度上是由于无法识别的高血压。 7%(95%CI 5.4-8.2%)的妇女错误地认为自己不是真正的禁忌者,主要是因为偏头痛的分类错误。在回归分析中,年轻女性,文化程度较高的女性和讲西班牙语的人更可能正确进行自我筛查(P <.05)。结论:使用医学检查表对口服避孕药的禁忌症进行自我筛查相对准确。无助的筛查是不准确的,并且反映出对口服避孕药安全性的普遍误解。非处方提供这种方法可能是安全的,特别是对于年轻妇女,如果鼓励独立进行血压筛查。

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