دورية أكاديمية

Tolerability of trivalent inactivated influenza vaccine among pregnant women, 2015

التفاصيل البيبلوغرافية
العنوان: Tolerability of trivalent inactivated influenza vaccine among pregnant women, 2015
المؤلفون: Suvanna Asavapiriyanont, Wanitchaya Kittikraisak, Piyarat Suntarattiwong, Darunee Ditsungnoen, Surasak Kaoiean, Podjanee Phadungkiatwatana, Nattinee Srisantiroj, Tawee Chotpitayasunondh, Fatimah S. Dawood, Kim A. Lindblade
المصدر: BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-7 (2018)
بيانات النشر: BMC, 2018.
سنة النشر: 2018
المجموعة: LCC:Gynecology and obstetrics
مصطلحات موضوعية: Tolerability, Influenza, Vaccination, Pregnant women, Thailand, Gynecology and obstetrics, RG1-991
الوصف: Abstract Background Thailand recommends influenza vaccination among pregnant women. We conducted a cohort study to determine if the prevalence of adverse events following immunization (AEFIs) with influenza vaccine among Thai pregnant women was similar to that often cited among healthy adults. Methods Women who were ≥17 gestational weeks and ≥18 years of age were recruited. Demographic and health history data were collected using structured questionnaires. Women were provided with symptom diary, ruler to measure local reaction(s), and thermometer to measure body temperature. AEFIs were defined as any new symptom/abnormality occurring within four weeks after vaccination. The diaries were abstracted for frequency, duration, and level of discomfort/inconvenience of the AEFIs. Serious adverse events (SAEs) and the likelihood of AEFIs being associated with vaccination were determined using standard definitions. Results Among 305 women enrolled between July–November 2015, median age was 29 years. Of these, 223 (73%) were in their third trimester, 271 (89%) had completed secondary school or higher, and 20 (7%) reported ≥1 pre-existing conditions. AEFIs were reported in 134 women (44%; 95% confidence interval [CI] 38–50%). Soreness at the injection site (74, 24%; CI 19–29%), general weakness (50, 16%; CI 12–21%), muscle ache (49, 16%; CI 12–21%), and headache (45, 15%; CI 1–19%) were most common. Of those with AEFIs, 120 (89%) reported symptom/abnormality occurred on day 0 or day 1 following vaccination. Ten women (7%) reported the AEFIs affected daily activities. The AEFIs generally spontaneously resolved within 24 h of onset. There were two vaccine-unrelated SAEs. Of 294 women with complete follow-up, 279 (95%) had term deliveries, 12 (4%) had preterm deliveries, and 3 (1%) had miscarriage or stillbirth. Conclusion In our cohort, AEFIs with influenza vaccine occurred with similar frequency to those reported among healthy adults in other studies, and were generally mild and self-limited. No influenza vaccine-associated SAEs were identified.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2393
العلاقة: http://link.springer.com/article/10.1186/s12884-018-1712-6Test; https://doaj.org/toc/1471-2393Test
DOI: 10.1186/s12884-018-1712-6
الوصول الحر: https://doaj.org/article/8ae084ac8e234dcd97663e336af8e214Test
رقم الانضمام: edsdoj.8ae084ac8e234dcd97663e336af8e214
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712393
DOI:10.1186/s12884-018-1712-6