Management of Tubo-ovarian Abscess: a Single Center Experience

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

82 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-01-01

Study Completion Date

2020-11-01

Brief Summary

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Electronic database of our tertiary obstetrics and gynecology clinic was searched for patients who were treated for tub-ovarian abscess during the last 10 years (January 2010- November 2020). Patients' biometric data, admission date and duration, medical and surgical treatment modalities were recorded using an Excel sheet. Patients will be evaluated on the basis of the treatment they receive, length of treatment, if surgically treatment the type of surgery performed. Hospitalization length, readmission, recurrence will be compared between treatment modalities.

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Detailed Description

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This retrospective study is conducted at Health Sciences University Turkey, Sisli Hamidiye Etfal Training and Research Hospital Department of Obstetrics and Gynecology. Electronic database was searched for patients who were treated for tub-ovarian abscess during the last 10 years (January 2010- November 2020). Patients' biometric data, admission date and duration, medical and surgical treatment modalities were recorded using an Excel sheet. Patients will be evaluated on the basis of the treatment they receive, length of treatment, if surgically treatment the type of surgery performed. Hospitalization length, readmission, recurrence will be compared between treatment modalities. A change in management strategy over the years if any will be reported.

Conditions

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Tubo-ovarian Abscess

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Interventions

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tuboovarian abscess

Evaluating the surgical and medical management of tuboovarian abscess

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* presence of a pelvic mass \> 3 cm with transvaginal ultrasound or magnetic resonance imaging indication abscess
* cervical and uterine tenderness
* abdominal rebound-defense under physical examination indication peritoneal irritation
* presence of symptoms such as fever, pelvic pain and increase in laboratory infection parameters

Exclusion Criteria

* Patients with known malignities
* Patients with incomplete data in the clinic's electronic database
* Patients who continued their treatment at other centers

Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No