Association Between Stroke and Patients With Pelvic Inflammatory Disease A Nationwide Population-Based Study in Taiwan

被引:18
作者
Chen, Po-Chih [2 ,3 ]
Tseng, Teng-chu [4 ]
Hsieh, Jui-Yang [5 ]
Lin, Hui-Wen [1 ,6 ]
机构
[1] Taipei Med Univ, Biostat & Res Consultat Ctr, Taipei, Taiwan
[2] Taipei Med Univ, Shung Ho Hosp, Dept Neurol, Taipei, Taiwan
[3] Taipei Med Univ, Shung Ho Hosp, Sleep Ctr, Taipei, Taiwan
[4] Sijhih Cathay Gen Hosp, Div Infect Dis, Taipei, Taiwan
[5] Min Sheng Gen Hosp, Dept Orthoped, Tao Yuan, Taiwan
[6] Natl Yang Ming Univ, Inst Publ Hlth, Taipei 112, Taiwan
关键词
epidemiology; pelvic inflammatory disease; risk factors; sensitivity analysis; stroke; ATHEROSCLEROSIS; RISK;
D O I
10.1161/STROKEAHA.110.612655
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-The aim of this study is to estimate the risk of stroke in a 3-year period after pelvic inflammatory disease (PID) using a nationwide population-based study. Methods-Our study cohort consisted of all patients with a diagnosis of PID (N=64 515) between 2004 and 2005 with a control cohort (1:2) of age-matched controls (N=129 030). Each patient was tracked from hospitalization until the end of 2006. Cox regressions were performed to compute the 3-year stroke-free survival rates after adjusting for possible confounding factors. Results-We found that women with PID were more likely to have strokes than the control population. After adjusting for potential confounding factors, the adjusted hazard ratio of stroke was 1.63 (95% CI, 1.45-1.85) for PID patients as compared to the general population cohort. Sensitivity analysis using a bootstrap approach further ensured the validity of the results of our study. Conclusions-We concluded that patients with PID have an association with stroke. Further research is necessary to investigate the pathophysiology between PID and stroke. (Stroke. 2011; 42: 2074-2076.)
引用
收藏
页码:2074 / 2076
页数:3
相关论文
共 11 条
[1]  
EFRON B., 1993, INTRO BOOTSTRAP, P168, DOI DOI 10.1007/978-1-4899-4541-9
[2]   Semi-automated sensitivity analysis to assess systematic errors in observational data [J].
Lash, TL ;
Fink, AK .
EPIDEMIOLOGY, 2003, 14 (04) :451-458
[3]  
LEE NC, 1991, OBSTET GYNECOL, V77, P425
[4]   Inflammation and atherosclerosis: Role of C-reactive protein in risk assessment [J].
Libby, P ;
Ridker, PM .
AMERICAN JOURNAL OF MEDICINE, 2004, 116 :9-16
[5]   Inflammation and atherosclerosis [J].
Libby, P ;
Ridker, PM ;
Maseri, A .
CIRCULATION, 2002, 105 (09) :1135-1143
[6]   Infection and inflammation induce LDL oxidation in vivo [J].
Memon, RA ;
Staprans, I ;
Noor, M ;
Holleran, WM ;
Uchida, Y ;
Moser, AH ;
Feingold, KR ;
Grunfeld, C .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (06) :1536-1542
[7]   Inflammatory biomarkers, hormone replacement therapy, and incident coronary heart disease - Prospective analysis from the Women's Health Initiative observational study [J].
Pradhan, AD ;
Manson, JE ;
Rossouw, JE ;
Siscovick, DS ;
Mouton, CP ;
Rifai, N ;
Wallace, RB ;
Jackson, RD ;
Pettinger, MB ;
Ridker, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (08) :980-987
[8]   Predisposition to atherosclerosis by infections role of endothelial dysfunction [J].
Prasad, A ;
Zhu, JH ;
Halcox, JPJ ;
Waclawiw, MA ;
Epstein, SE ;
Quyyumi, AA .
CIRCULATION, 2002, 106 (02) :184-190
[9]   The association of interleukin 6 with clinical and laboratory parameters of acute pelvic inflammatory disease [J].
Richter, HE ;
Holley, RL ;
Andrews, WW ;
Owen, J ;
Miller, KB .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1999, 181 (04) :940-944
[10]   Accelerated atherosclerosis in autoimmune rheumatic diseases [J].
Shoenfeld, Y ;
Gerli, R ;
Doria, A ;
Matsuura, E ;
Cerinic, MM ;
Ronda, N ;
Jara, LJ ;
Abu-Shakra, M ;
Meroni, PL ;
Sherer, Y .
CIRCULATION, 2005, 112 (21) :3337-3347