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Gynecologic Oncology
Volume 110, Issue 1, July 2008, Pages 60-64
 
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doi:10.1016/j.ygyno.2008.02.011    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2008 Elsevier Inc. All rights reserved.

Validation of FACT/GOG-AD subscale for ovarian cancer-related abdominal discomfort: A Gynecologic Oncology Group studystar, open, star, open, star, open

Lari Wenzela, Corresponding Author Contact Information, E-mail The Corresponding Author, Helen Q. Huangb, David Cellac, Joan L. Walkerd, e and Deborah K. Armstrongf

aUniversity of California, Irvine, Irvine, CA 92697, USA bGynecologic Oncology Group Statistical and Data Center, Buffalo, NY 14263, USA cCenter for Outcomes, Research and Education, Evanston Northwestern Healthcare and Northwestern University, Evanston, IL 60201, USA dDepartment of Obstetrics and Gynecology, University of Oklahoma, Oklahoma City, OK 73190, USA eDepartment of Gynecologic Oncology, University of Oklahoma, Oklahoma City, OK 73190, USA fDepartment of Oncology, Gynecology and Obstetrics, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA

Received 7 August 2007. 
Available online 21 April 2008.

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Abstract

Objective

To evaluate the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Abdominal Discomfort (FACT/GOG-AD) subscale for assessing abdominal discomfort in patients undergoing treatment for ovarian cancer.

Methods

A four-item questionnaire was developed for use in Gynecologic Oncology Group (GOG) protocol 172. It was administered to patients with advanced ovarian cancer treated on this protocol with intravenous (IV) cisplatin/paclitaxel or a combination of intravenous and intraperitoneal (IP) cisplatin/paclitaxel (IV/IP) prior to randomization, before cycle 4, 3–6 weeks after cycle 6, and 12 months after cycle 6. The subscale was evaluated in patients receiving IV/IP therapy for internal consistency, concurrent validity, sensitivity to treatment differences, and responsiveness to abdominal discomfort grading.

Results

Internal consistency coefficients were 0.83 and 0.87 at baseline and pre-cycle 4 assessments, respectively; the average inter-item correlation was 0.61 at the pre-cycle 4 assessment. Item correlation with other scales ranged from 0.00–0.44. This subscale was able to distinguish those graded to have physician-rated abdominal pain compared to those without clinician-reported discomfort.

Conclusion

The four-item AD subscale reliably and validly assesses ovarian cancer-specific abdominal discomfort, and captures abdominal symptom responses to IV and IV/IP cisplatin/paclitaxel treatments.

Keywords: Measurement tool; Abdominal discomfort; Self-assessment

Article Outline

Introduction
Methods
Patients and treatment
FACT/GOG-AD subscale
Abdominal discomfort assessments
Statistical considerations
Reliability
Construct validity
Responsiveness to change over time
Sensitivity to abdominal discomfort grading
Results
Patient characteristics
Assessment completion
Psychometric properties of the AD subscale
Internal consistency
Construct validity
Sensitivity to abdominal discomfort grading
Responsiveness to change over time
Discussion
Conflict of interest statement
References

 
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