Do short-term markers of treatment efficacy predict long-term sequelae of pelvic inflammatory disease?

Objective This study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease, predict sequelae of lack of pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain. Study Design Women with mild-to-modera...

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Published inAmerican journal of obstetrics and gynecology Vol. 198; no. 1; pp. 30.e1 - 30.e7
Main Authors Trautmann, Gail M., MA, Kip, Kevin E., MPH, PhD, Richter, Holly E., PhD, MD, Soper, David E., MD, Peipert, Jeffrey F., MD, MPH, Nelson, Deborah B., PhD, Trout, Wayne, MD, Schubeck, Dianne, MD, Bass, Debra C., MS, Ness, Roberta B., MD, MPH
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LanguageEnglish
Published Philadelphia, PA Mosby, Inc 2008
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Abstract Objective This study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease, predict sequelae of lack of pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain. Study Design Women with mild-to-moderate pelvic inflammatory disease were assessed after treatment initiation at 5 days for tenderness (n = 713) and at 30 days for tenderness, cervical infections and endometritis (n = 298). Pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain were evaluated after 84 months, on average. Results Pelvic tenderness at 5 and at 30 days significantly elevated the risk for developing chronic pelvic pain; tenderness at 30 days was also significantly associated with recurrent pelvic inflammatory disease. However, pelvic tenderness at 5 and at 30 days was only modestly clinically predictive of chronic pelvic pain or recurrent pelvic inflammatory disease (positive predictive values 22.1-66.9%). No short-term marker significantly influenced the likelihood of achieving a pregnancy. Conclusion Tenderness at 5 or 30 days did not accurately predict the occurrence of pelvic inflammatory disease-related reproductive morbidities.
AbstractList This study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease, predict sequelae of lack of pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain. Women with mild-to-moderate pelvic inflammatory disease were assessed after treatment initiation at 5 days for tenderness (n = 713) and at 30 days for tenderness, cervical infections and endometritis (n = 298). Pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain were evaluated after 84 months, on average. Pelvic tenderness at 5 and at 30 days significantly elevated the risk for developing chronic pelvic pain; tenderness at 30 days was also significantly associated with recurrent pelvic inflammatory disease. However, pelvic tenderness at 5 and at 30 days was only modestly clinically predictive of chronic pelvic pain or recurrent pelvic inflammatory disease (positive predictive values 22.1-66.9%). No short-term marker significantly influenced the likelihood of achieving a pregnancy. Tenderness at 5 or 30 days did not accurately predict the occurrence of pelvic inflammatory disease-related reproductive morbidities.
OBJECTIVEThis study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease, predict sequelae of lack of pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain.STUDY DESIGNWomen with mild-to-moderate pelvic inflammatory disease were assessed after treatment initiation at 5 days for tenderness (n = 713) and at 30 days for tenderness, cervical infections and endometritis (n = 298). Pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain were evaluated after 84 months, on average.RESULTSPelvic tenderness at 5 and at 30 days significantly elevated the risk for developing chronic pelvic pain; tenderness at 30 days was also significantly associated with recurrent pelvic inflammatory disease. However, pelvic tenderness at 5 and at 30 days was only modestly clinically predictive of chronic pelvic pain or recurrent pelvic inflammatory disease (positive predictive values 22.1-66.9%). No short-term marker significantly influenced the likelihood of achieving a pregnancy.CONCLUSIONTenderness at 5 or 30 days did not accurately predict the occurrence of pelvic inflammatory disease-related reproductive morbidities.
Objective This study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease, predict sequelae of lack of pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain. Study Design Women with mild-to-moderate pelvic inflammatory disease were assessed after treatment initiation at 5 days for tenderness (n = 713) and at 30 days for tenderness, cervical infections and endometritis (n = 298). Pregnancy, recurrent pelvic inflammatory disease, and chronic pelvic pain were evaluated after 84 months, on average. Results Pelvic tenderness at 5 and at 30 days significantly elevated the risk for developing chronic pelvic pain; tenderness at 30 days was also significantly associated with recurrent pelvic inflammatory disease. However, pelvic tenderness at 5 and at 30 days was only modestly clinically predictive of chronic pelvic pain or recurrent pelvic inflammatory disease (positive predictive values 22.1-66.9%). No short-term marker significantly influenced the likelihood of achieving a pregnancy. Conclusion Tenderness at 5 or 30 days did not accurately predict the occurrence of pelvic inflammatory disease-related reproductive morbidities.
Author Bass, Debra C., MS
Kip, Kevin E., MPH, PhD
Nelson, Deborah B., PhD
Trout, Wayne, MD
Richter, Holly E., PhD, MD
Trautmann, Gail M., MA
Soper, David E., MD
Peipert, Jeffrey F., MD, MPH
Schubeck, Dianne, MD
Ness, Roberta B., MD, MPH
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Issue 1
Keywords treatment
chronic pain
adnexitis
chlamydia
prediction
endometritis
infertility
recurrent pelvic inflammatory disease
Short term
Treatment
Treatment efficiency
Gynecology
Prediction
Biological marker
Salpingitis
Predictive factor
Long term
Obstetrics
Female genital diseases
Fallopian tube pathology
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SSID ssj0002292
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Snippet Objective This study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease,...
This study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease, predict...
OBJECTIVEThis study was undertaken to assess whether short-term markers, often used to measure clinical cure after treatment for pelvic inflammatory disease,...
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SubjectTerms Administration, Oral
adnexitis
Adolescent
Adult
Bacterial diseases
Bacterial diseases of the genital system
Biological and medical sciences
Cefoxitin - administration & dosage
chlamydia
chronic pain
Dose-Response Relationship, Drug
Doxycycline - administration & dosage
Drug Administration Schedule
Drug Therapy, Combination
endometritis
Female
Follow-Up Studies
Gynecology. Andrology. Obstetrics
Human bacterial diseases
Humans
Infectious diseases
infertility
Infertility, Female
Inflammation Mediators - analysis
Infusions, Intravenous
Medical sciences
Obstetrics and Gynecology
Pain Measurement
Pelvic Inflammatory Disease - diagnosis
Pelvic Inflammatory Disease - drug therapy
prediction
Predictive Value of Tests
Probability
Probenecid - administration & dosage
Proportional Hazards Models
Recurrence
recurrent pelvic inflammatory disease
Severity of Illness Index
Time Factors
treatment
Treatment Outcome
Title Do short-term markers of treatment efficacy predict long-term sequelae of pelvic inflammatory disease?
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0002937807006357
https://dx.doi.org/10.1016/j.ajog.2007.05.021
https://www.ncbi.nlm.nih.gov/pubmed/18166300
https://search.proquest.com/docview/70173363
Volume 198
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