To determine reference values for postvoid residual (PVR) volume for patients referred to a tertiary urogynecology center.
After Institutional Review Board approval, we performed a retrospective chart review of all new patients presenting to our referral center. We assessed associations between PVR and patient demographics, pelvic floor symptoms, and physical examination by Wilcoxon rank sum or Kruskal-Wallis tests as appropriate. A multivariable logistic regression model was used to calculate odds ratios for patient characteristics associated with PVR in the top age range-specific decile.
Three hundred sixty-one patients were included in the analysis. The median PVR was 20 mL (interquartile range, 1st, 3rd quartiles, 10, 50). Older age was associated with higher PVR (P < 0.001). The median PVR in participants younger than 40 years was 10 mL, ages 40 to 49 years was 18 mL, 50 to 69 years was 20 mL, 70 to 79 years was 38 mL and in women older than 79 years was 50 mL. A multivariable analysis showed that prolapse stage (odds ratio [OR], 3.46 with prolapse stage 2–4 vs stage 0–1; P = 0.001), history of stroke (OR, 7.62; [95% CI 2.17–26.77, P = 0.002]), narcotic use (OR, 2.45; [95% CI 1.01–5.92; P = 0.047]), and urinary frequency (OR, 2.61; [95% CI, 1.14–5.98; P = 0.024]) were risk factors for increased PVR (as defined at >90%ile for age), independent of the age-related elevation.
The majority of patients presenting for urogynecologic evaluation had a low PVR with a median of 20 mL. Postvoid residual was higher for older age groups but nearly all volumes were less than 100 mL. The utility of a PVR measurement is highest for patients with pelvic organ prolapse, urinary frequency, narcotic use, or history of stroke.
From the *Division of Urogynecology, Department of Obstetrics/Gynecology and Urology, Loyola University Chicago Stritch School of Medicine and Loyola University Medical Center,
†Loyola University Chicago Stritch School of Medicine,
‡Biostatistics Core, Public Health Sciences, Division Center for Translational Research and Education, Loyola University Chicago Stritch School of Medicine, Maywood; and
§Department of Obstetrics/Gynecology and Surgery, Rush University Medical Center, Chicago, IL.
The authors have declared they have no conflicts of interest.
B.J. participated in the research design, planning, data collection and article writing. K.B. participated in the research planning, data collection, and article editing. C.J.J. participated in the data analysis and article writing. M.S. participated in the research design, planning, and article editing. C.A.B. participated in the research design, planning, and article writing.
Correspondence: Birte Johanna Wolff, MD, 2160 S First Ave., Maywood, IL 60153. E-mail: Birte.email@example.com.