Antibodies to the chlamydial 60 kd heat-shock protein are associated with laparoscopically confirmed perihepatitis

OBJECTIVE: Our purpose was to examine clinical, microbiologic, serologic, and laparoscopic findings associated with perihepatitis. STUDY DESIGN: In a prospective study of 157 women with a clinical diagnosis of pelvic inflammatory disease, 27 women with laparoscopically confirmed perihepatitis and sa...

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Veröffentlicht in:American journal of obstetrics and gynecology 1997-04, Vol.176 (4), p.870-877
Hauptverfasser: Money, Deborah M., Hawes, Stephen E., Eschenbach, David A., Peeling, Rosanna W., Brunham, Robert, Wölner-Hanssen, Pal, Stamm, Walter E.
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Sprache:eng
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Zusammenfassung:OBJECTIVE: Our purpose was to examine clinical, microbiologic, serologic, and laparoscopic findings associated with perihepatitis. STUDY DESIGN: In a prospective study of 157 women with a clinical diagnosis of pelvic inflammatory disease, 27 women with laparoscopically confirmed perihepatitis and salpingitis were compared with 46 patients with salpingitis alone. RESULTS: Both current use or a history of ever using oral contraceptives was negatively associated with perihepatitis ( p = 0.05 and p = 0.008, respectively). Moderate-to-severe pelvic adhesions were present at laparoscopy significantly more often in the perihepatitis-salpingitis group (70%) than in the salpingitis alone group (35%, p = 0.003). Antibody to the chlamydial 60 kd heat-shock protein at ≥0.5 optical density was detected in 67% of the perihepatitis-salpingitis group and in 28% of the salpingitis alone group ( p = 0.005), and the median titer was significantly higher in the former group ( p = 0.02). CONCLUSION: Compared with women with salpingitis alone, patients with perihepatitis-salpingitis do not have distinctive clinical or microbiologic findings but do manifest a higher prevalence of moderate-to-severe pelvic adhesions and both a higher prevalence and higher titers of antibody to the chlamydial heat-shock protein-60. (Am J Obstet Gynecol 1997;176:870-7.)
ISSN:0002-9378
1097-6868
DOI:10.1016/S0002-9378(97)70613-6