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利用推特数据进行孕期药物安全性队列研究:以β受体阻滞剂为例的概念验证

Using Twitter Data for Cohort Studies of Drug Safety in Pregnancy: Proof-of-concept With β-Blockers.

作者信息

Klein Ari Z, O'Connor Karen, Levine Lisa D, Gonzalez-Hernandez Graciela

机构信息

Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.

Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.

出版信息

JMIR Form Res. 2022 Jun 30;6(6):e36771. doi: 10.2196/36771.

Abstract

BACKGROUND

Despite the fact that medication is taken during more than 90% of pregnancies, the fetal risk for most medications is unknown, and the majority of medications have no data regarding safety in pregnancy.

OBJECTIVE

Using β-blockers as a proof-of-concept, the primary objective of this study was to assess the utility of Twitter data for a cohort study design-in particular, whether we could identify (1) Twitter users who have posted tweets reporting that they took medication during pregnancy and (2) their associated pregnancy outcomes.

METHODS

We searched for mentions of β-blockers in 2.75 billion tweets posted by 415,690 users who announced their pregnancy on Twitter. We manually reviewed the matching tweets to first determine if the user actually took the β-blocker mentioned in the tweet. Then, to help determine if the β-blocker was taken during pregnancy, we used the time stamp of the tweet reporting intake and drew upon an automated natural language processing (NLP) tool that estimates the date of the user's prenatal time period. For users who posted tweets indicating that they took or may have taken the β-blocker during pregnancy, we drew upon additional NLP tools to help identify tweets that report their pregnancy outcomes. Adverse pregnancy outcomes included miscarriage, stillbirth, birth defects, preterm birth (<37 weeks gestation), low birth weight (<5 pounds and 8 ounces at delivery), and neonatal intensive care unit (NICU) admission. Normal pregnancy outcomes included gestational age ≥37 weeks and birth weight ≥5 pounds and 8 ounces.

RESULTS

We retrieved 5114 tweets, posted by 2339 users, that mention a β-blocker, and manually identified 2332 (45.6%) tweets, posted by 1195 (51.1%) of the users, that self-report taking the β-blocker. We were able to estimate the date of the prenatal time period for 356 pregnancies among 334 (27.9%) of these 1195 users. Among these 356 pregnancies, we identified 257 (72.2%) during which the β-blocker was or may have been taken. We manually verified an adverse pregnancy outcome-preterm birth, NICU admission, low birth weight, birth defects, or miscarriage-for 38 (14.8%) of these 257 pregnancies. We manually verified a gestational age ≥37 weeks for 198 (90.4%) and a birth weight ≥5 pounds and 8 ounces for 50 (22.8%) of the 219 pregnancies for which we did not identify an adverse pregnancy outcome.

CONCLUSIONS

Our ability to detect pregnancy outcomes for Twitter users who posted tweets reporting that they took or may have taken a β-blocker during pregnancy suggests that Twitter can be a complementary resource for cohort studies of drug safety in pregnancy.

摘要

背景

尽管超过90%的孕期女性会服用药物,但大多数药物对胎儿的风险尚不清楚,并且大多数药物没有关于孕期安全性的数据。

目的

以β受体阻滞剂作为概念验证,本研究的主要目的是评估推特数据在队列研究设计中的效用——特别是,我们能否识别出(1)发布推文报告自己在孕期服用过药物的推特用户,以及(2)他们相应的妊娠结局。

方法

我们在415,690名在推特上宣布怀孕的用户发布的27.5亿条推文中搜索提及β受体阻滞剂的内容。我们人工审核匹配的推文,首先确定用户是否真的服用了推文中提到的β受体阻滞剂。然后,为了帮助确定β受体阻滞剂是否在孕期服用,我们使用了报告服药情况的推文的时间戳,并借助一种自动化自然语言处理(NLP)工具来估计用户产前时间段的日期。对于发布推文表明自己在孕期服用或可能服用了β受体阻滞剂的用户,我们借助其他NLP工具来帮助识别报告其妊娠结局的推文。不良妊娠结局包括流产、死产、出生缺陷、早产(妊娠<37周)、低出生体重(出生时<5磅8盎司)以及新生儿重症监护病房(NICU)收治。正常妊娠结局包括孕周≥37周且出生体重≥5磅8盎司。

结果

我们检索到2339名用户发布的5114条提及β受体阻滞剂的推文,并人工识别出1195名(51.1%)用户发布的2332条(45.6%)推文,这些推文自我报告服用了β受体阻滞剂。我们能够估计这1195名用户中334名(27.9%)的356次妊娠的产前时间段日期。在这356次妊娠中,我们识别出257次(72.2%)在孕期服用或可能服用了β受体阻滞剂。我们人工核实了这257次妊娠中有38次(14.8%)出现不良妊娠结局——早产、NICU收治、低出生体重、出生缺陷或流产。对于我们未识别出不良妊娠结局的219次妊娠,我们人工核实出198次(90.4%)的孕周≥37周,50次(22.8%)的出生体重≥5磅8盎司。

结论

对于发布推文报告自己在孕期服用或可能服用了β受体阻滞剂的推特用户,我们有能力检测其妊娠结局,这表明推特可以成为孕期药物安全性队列研究的一种补充资源。

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