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Dive into the research topics where Deborah Draper is active.

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Featured researches published by Deborah Draper.


American Journal of Obstetrics and Gynecology | 1979

Use of laparoscopy to determine the microbiologic etiology of acute salpingitis

Richard L. Sweet; John A. Mills; Keith W. Hadley; Edward Blumenstock; Julius Schachter; Marilyn O. Robbie; Deborah Draper

To determine the microbiologic etiology of acute salpingitis, laparoscopy was used in 26 patients to obtain specimens for a variety of microorganisms directly from the fallopian tube. Simultaneous culdocentesis was performed to obtain peritoneal fluid for microbiologic analysis. A variety of microorganisms were isolated from the fallopian tubes and cul-de-sac aspirate. However, the organisms isolated from the fallopian tube were not consistent with the cul-de-sac isolates. It appears that direct culture from the fallopian tube may be necessary to determine the microbiologic etiology and pathogenesis of acute salpingitis. N. gonorrhoeae was isolated from the cul-de-sac in 32 per cent of cases and the fallopian tube in 19 per cent. In patients with endocervical gonorrhea, the gonococcus was isolated from the fallopian tube in 38.5 per cent of cases. Aerobic and/or anaerobic bacteria were present in the cul-de-sac aspirate in 46 per cent of patients and in the fallopian tube in 38 per cent.


The Journal of Infectious Diseases | 1998

Cysteine Proteases of Trichomonas vaginalis Degrade Secretory Leukocyte Protease Inhibitor

Deborah Draper; William Donohoe; Leo Mortimer; R. Phillip Heine

Sexually transmitted diseases, including trichomoniasis, are risk factors for acquisition of human immunodeficiency virus (HIV) infection. Enhancement mechanisms are unknown. Secretory leukocyte protease inhibitor (SLPI) from saliva appears to prevent transmission of HIV through inhibition of virus entry into monocytic cells in vitro. This study was undertaken to determine if secreted cysteine proteases of Trichomonas vaginalis degrade SLPI and render it nonfunctional. It was determined if SLPI levels were decreased in vaginal fluids from pregnant women infected with T. vaginalis. Isolated proteases were incubated with recombinant human SLPI, and the degradation was followed by Western analysis with SLPI antiserum. SLPI levels were measured by ELISA in vaginal fluids from women infected with T. vaginalis and uninfected controls. Cysteine proteases cleaved SLPI and rendered it nonfunctional. Median levels of SLPI from infected patients were 26% of those of controls (P <.005). The degradation of SLPI in association with trichomonal infection may increase the risk of HIV acquisition.


American Journal of Obstetrics and Gynecology | 1992

Association of cervicovaginal infections with increased vaginal fluid phospholipase A2 activity

James A. McGregor; Janice I. French; Ward Jones; Ruth Parker; Elisa Patterson; Deborah Draper

Abstract OBJECTIVE: The purpose of this study was to determine if phospholipase A 2 was detectable within vaginal fluid and to correlate its presence with the presence of common lower genital tract infection or microbial conditions. STUDY DESIGN: Pregnant women were examined at the first prenatal visit with standard clinical evaluations and microbiologic cultures or tests. Vaginal fluid samples were evaluated for phospholipase A 2 activity by means of a standardized enzyme fluorometric assay. Data were stratified to control for coexisting infections. RESULTS: Phospholipase A 2 activity was detected among 29.8% of women and was independently associated with the presence of bacterial vaginosis ( p p Chlamydia trachomatis ( p 2 activity and the level of activity was increased in the presence of more than one infection. CONCLUSIONS: Elevated reproductive tract phospholipase A 2 concentrations among pregnant women may play roles in the pathogenesis of preterm labor and birth. Identification of pregnant women with increased concentrations in vaginal fluid may allow for development of effective intervention strategies to reduce the risk of preterm birth. (AM J OBSTET GYNECOL 1992;167:1588-94.)


Infectious Diseases in Obstetrics & Gynecology | 1995

Trichomonas vaginalis Weakens Human Amniochorion in an In Vitro Model of Premature Membrane Rupture

Deborah Draper; Ward Jones; R. Phillip Heine; Michelle Beutz; Janice I. French; James A. McGregor

Objective: Trichomonas vaginalis (TV) infection is associated with preterm rupture of membranes (PROM) and preterm birth. We evaluated the effects of TV growth and metabolism on preparations of human amniochorion to understand and characterize how TV may impair fetal-membrane integrity and predispose to PROM and preterm birth. Methods: Term fetal membranes were evaluated using an established in vitro fetal-membrane model. Fresh TV clinical isolates were obtained from pregnant women. The protozoa (5.0×105 to 1.5×106/ml) were incubated with fetal membranes in modified Diamonds medium for 20 h at 37°C in 5% CO2.The effects of fetal-membrane strength (bursting tension, work to rupture, and elasticity) were measured using a calibrated Wheatstone-bridge dynamometer. Tests were also performed to evaluate the effects of 1) inoculum size; 2) metronidazole (50 μg/ml); and 3) cell-free filtrate. Results: The TV-induced membrane effects were 1) isolate variable; 2) inoculum dependent; 3) incompletely protected by metronidazole; and 4) mediated by both live organisms as well as protozoan-free culture filtrates. Six of 9 isolates significantly reduced the calculated work to rupture (P ≤ 0.02); 7 of 9 reduced bursting tension; and 1 of 9 reduced elasticity. One isolate significantly increased the work to rupture and bursting tension (P ≤ 0.002). Conclusions: In vitro incubation of fetal membranes with TV can significantly impair the measures of fetal-membrane strength. This model may be used to delineate the mechanisms of TV-induced membrane damage. This study suggests that there are enzyme-specific effects as well as pH effects.


Infectious Diseases in Obstetrics & Gynecology | 1994

Trichomonas vaginalis: Diagnosis and Clinical Characteristics in Pregnancy

R. Phillip Heine; James A. McGregor; Elisa Patterson; Deborah Draper; Janice I. French; Ward Jones

Objective: The objectives of this study were to 1) determine the prevalance and characterize the symptomatology of Trichomonas vaginalis (TV) infection in pregnant women on entry into prenatal care in an inner-city population; 2) compare conventional microscopic methods vs. culture techniques in diagnosing TV in both symptomatic and asymptomatic pregnant patients; and 3) correlate wet mount microscopic and microbiologic characteristics of varying manifestations of trichomoniasis. Methods: One thousand two hundred sixty patients in an inner-city population were tested at entry into prenatal care for TV by saline wet mount and culture techniques. Other tests for lower genital tract infection were also performed. Vaginal symptoms were ascertained through standardized questioning prior to examination. Standard microscopic and microbiologic data were also obtained for analysis. Wet mounts were systematically examined and considered negative if no TV was identified in 10 high powerfields (HPFs). Cultures were inspected from days 4 to 7 or until positive results were obtained. Results were analyzed using McNemars test for correlated proportions, chi-squared test, or Fisher exact test where appropriate. Results: Culture and wet mount results were available in 1,175 patients. TV infection was documented by one or both techniques in 110/1,175 (9.4%). Culture methods detected 105/110 (94.5%) of all patients while wet mount detected 90/110 (73%) (P <0.001). Vaginal symptoms were present in only 20/110 patents (18.2%). Among asymptomatic patients, culture detected 94% while wet mount detected 70% (P < 0.001). Among symptomatic patients, wet mount and culture were both effective and diagnosed 85% and 95% of infections, respectively (P = not significant). Patients with TV were more likely to have increased vaginal fluid wlaite blood cells (WBCs) and more severe vaginal flora disruption than uninfected controls. Subgroup analysis revealed wet mount-positive/culture-positive patients were more likely to have vaginal flora disruption, as evidenced by decreased lactobacilli and elevated vaginal pH, than wet mount-negative/culture-positive subjects. Coexistent infection rates were similar regardless of wet mount status. Elevated vaginal fluid WBCs were more common among patients with symptoms. Conclusions: 1) Screening pregnant women for TV based solely on symptomatology is ineffective in this population; 2) culture techniques detected more infections than conventional microscopic evaluation; and 3) significant increases in vaginal fluid WBCs and altered vaginal flora are found in both symptomatic and asymptomatic TV, suggesting that both infestations have the potential to adversely affect pregnancy outcome. Studies on the influence of TV on pregnancy outcomes are ongoing.


American Journal of Obstetrics and Gynecology | 2000

Levels of vaginal secretory leukocyte protease inhibitor are decreased in women with lower reproductive tract infections

Deborah Draper; Daniel V. Landers; Marijane A. Krohn; Sharon L. Hillier; Harold C. Wiesenfeld; R. Phillip Heine


American Journal of Obstetrics and Gynecology | 1996

Evaluation of a deoxyribonucleic acid probe for the detection of Trichomonas vaginalis in vaginal secretions

Lynette R. DeMeo; Deborah Draper; James A. McGregor; Douglas F. Moore; Christopher R. Peter; Peter Kapernick; William M. McCormack


American Journal of Obstetrics and Gynecology | 1980

In vitro modeling of acute salpingitis caused by Neisseria gonorrhoeae

Deborah Draper; Elizabeth Donegan; John F. James; Richard L. Sweet; George F. Brooks


/data/revues/00029378/v173i1/0002937895901841/ | 2011

Prevention of premature birth by screening and treatment for common genital tract infections: Results of a prospective controlled evaluation

James A. McGregor; Janice I. French; Ruth Parker; Deborah Draper; Elisa Patterson; Ward Jones; Kyja Thorsgard; John McFee


American Journal of Obstetrics and Gynecology | 1996

Reply to: Mechanisms of preterm premature rupture of membranes

Deborah Draper; R. Phillip Heine

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James A. McGregor

University of Colorado Boulder

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Ward Jones

Anschutz Medical Campus

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Ruth Parker

Anschutz Medical Campus

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Michelle Beutz

Boston Children's Hospital

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