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长航官兵胃食管反流病发病情况、危险因素及干预效果研究 被引量:5

Morbidity, risk factors, and intervention of gastroesophageal reflux disease in long-term sailors of navy
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摘要 目的研究长航官兵胃食管反流病(GERD)的发病情况及相关危险因素,观察相应干预措施的效果。方法456名长航官兵(男342例,女84例),于长航开始、8周后及16周分别进行3次问卷调查。长航8周后观察GERD的发病率变化,并采用Logistic回归进行危险因素分析。针对相应危险因素对长航官兵进行干预,时间为8周。8周后再次观察发病率的变化。结果收回3份有效问卷的人数422人(男319人,女73人)。长航8周后GERD发病率为27.5%,显著高于长航开始时(19.2%,P〈0.01,χ2=8.11)。单因素Logistic回归分析发现精神压力大、工作强度高、吸烟、晕船、肥胖、过饱饮食与GERD关系密切(均P〈0.05)。针对这些因素干预8周后GERD发病率为21.5%,显著低于长航8周时(0.01〈P〈0.05,χ2=4.34)。结论长航8周后GERD发病率显著增加。精神压力大、工作强度高、吸烟、晕船、肥胖、过饱饮食为胃食管反流病的危险因素。干预后GERD发病率降低。 Objective To investigate the morbidity, risk factors, and effects of intervention of gastroesophageal reflux disease (GERD) in long-term sailors of navy. Methods 456 long-term sailors of navy, 342 males and 84 females, underwent questionnaire survey thrice: at the beginning of long-term navigation, and 8 and 16 weeks after the long-term voyage. Logistic regression was used to analyze the morbidity, risk factors, and effects of intervention. Results 422 subjects, 319 males and 73 females completed 3 effective questionnaires. The morbidity of GERD 8 weeks after the long-term voyage was 27.5% , significantly higher than that at the beginning (19.2%, P 〈0.01, χ2=8.11). Logistic regression showed that mental stress, work intensity, smoking, seasickness, obesity, and overeating were all positively correlated with GERD (all P 〈0,05). The morbidity of GERD 16 weeks later, after intervention targetting the above-mentioined risk factors for 8 weeks, was 21.5%, significantly lower than that 8 weeks after the voyage (0.01 〈 P 〈 0.05, χ2=4.34). Conclusion The morbidity of GERD increases after long-term voyage. Mental stress, work intensity, smoking, seasickness, obesity, and overeating are relevant risk factors. Intervention works to decrease the morbidity.
出处 《中国急救复苏与灾害医学杂志》 2016年第2期146-148,共3页 China Journal of Emergency Resuscitation and Disaster Medicine
基金 全军医药卫生科研项目(CHJ11J018)
关键词 长航官兵 胃食管反流病 发病率 危险因素 干预 Long-term sailor of navy Gastroesophageal reflux disease: Morbidit: Risk factors: Intervention
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