Geller Andrew I, Shehab Nadine, Weidle Nina J, Lovegrove Maribeth C, Wolpert Beverly J, Timbo Babgaleh B, Mozersky Robert P, Budnitz Daniel S
From the Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention (A.I.G., N.S., M.C.L., D.S.B.), and Chenega Government Consulting (N.J.W.) - both in Atlanta; and the Center for Food Safety and Applied Nutrition and the Division of Public Health Informatics and Analytics (B.J.W., B.B.T.) and the Division of Dietary Supplement Programs (R.P.M.), Food and Drug Administration, College Park, MD.
N Engl J Med. 2015 Oct 15;373(16):1531-40. doi: 10.1056/NEJMsa1504267.
Dietary supplements, such as herbal or complementary nutritional products and micronutrients (vitamins and minerals), are commonly used in the United States, yet national data on adverse effects are limited.
We used nationally representative surveillance data from 63 emergency departments obtained from 2004 through 2013 to describe visits to U.S. emergency departments because of adverse events related to dietary supplements.
On the basis of 3667 cases, we estimated that 23,005 (95% confidence interval [CI], 18,611 to 27,398) emergency department visits per year were attributed to adverse events related to dietary supplements. These visits resulted in an estimated 2154 hospitalizations (95% CI, 1342 to 2967) annually. Such visits frequently involved young adults between the ages of 20 and 34 years (28.0% of visits; 95% CI, 25.1 to 30.8) and unsupervised children (21.2% of visits; 95% CI, 18.4 to 24.0). After the exclusion of unsupervised ingestion of dietary supplements by children, 65.9% (95% CI, 63.2 to 68.5) of emergency department visits for single-supplement-related adverse events involved herbal or complementary nutritional products; 31.8% (95% CI, 29.2 to 34.3) involved micronutrients. Herbal or complementary nutritional products for weight loss (25.5%; 95% CI, 23.1 to 27.9) and increased energy (10.0%; 95% CI, 8.0 to 11.9) were commonly implicated. Weight-loss or energy products caused 71.8% (95% CI, 67.6 to 76.1) of supplement-related adverse events involving palpitations, chest pain, or tachycardia, and 58.0% (95% CI, 52.2 to 63.7) involved persons 20 to 34 years of age. Among adults 65 years of age or older, choking or pill-induced dysphagia or globus caused 37.6% (95% CI, 29.1 to 46.2) of all emergency department visits for supplement-related adverse events; micronutrients were implicated in 83.1% (95% CI, 73.3 to 92.9) of these visits.
An estimated 23,000 emergency department visits in the United States every year are attributed to adverse events related to dietary supplements. Such visits commonly involve cardiovascular manifestations from weight-loss or energy products among young adults and swallowing problems, often associated with micronutrients, among older adults. (Funded by the Department of Health and Human Services.).
膳食补充剂,如草药或补充性营养产品以及微量营养素(维生素和矿物质),在美国被广泛使用,但关于其不良反应的全国性数据有限。
我们使用了2004年至2013年期间从63个急诊科获取的具有全国代表性的监测数据,以描述因与膳食补充剂相关的不良事件而前往美国急诊科就诊的情况。
基于3667例病例,我们估计每年有23,005次(95%置信区间[CI],18,611至27,398)急诊科就诊归因于与膳食补充剂相关的不良事件。这些就诊每年导致约2154例住院(95%CI,1342至2967)。此类就诊经常涉及20至34岁的年轻人(占就诊人数的28.0%;95%CI,25.1至30.8)和无人监管的儿童(占就诊人数的21.2%;95%CI,18.4至24.0)。在排除儿童无人监管摄入膳食补充剂的情况后,因单一补充剂相关不良事件前往急诊科就诊的患者中,65.9%(95%CI,63.2至68.5)涉及草药或补充性营养产品;31.8%(95%CI,29.2至