Infectious Diseases in Obstetrics and Gynecology
Volume 1 (1993), Issue 1, Pages 37-39
doi:10.1155/S1064744993000092
Clinical Study
Sheathing of the Endovaginal Ultrasound Probe:
Is It Adequate?
1Division of Maternal-Fetal Medicine, University of Florida College of Medicine, Gainesville, FL, USA
2Department of Obstetrics and Gynecology, University of Florida College of Medicine, P.O. Box 100294, Gainesville 32610-0294, FL, USA
Received 30 December 1992; Accepted 11 March 1993
Abstract
The purpose of this prospective investigation was to compare two methods for sheathing of the
endovaginal ultrasound-probe. The study was conducted over a 7-month period in 1991–1992. In the
first half of the investigation, latex examination gloves were used to sheath the endovaginal probe;
during the second half of the investigation, latex condoms were used. Following the ultrasound
examination, the probes were inspected for gross contamination by the ultrasonographer. The
sheaths were then tested for perforations by filling them with water to twice their usual volume and
observing for leaks. Fifty unused gloves and condoms were similarly tested to determine the prevalence
of preexisting defects. One hundred twenty-eight gloves and 102 condoms from patients were
tested. Four gloves (3.1%, 95% C.I. 1.6–4.6%) and seven condoms (6.9%, 95% C.I. 4.4–9.4%) had
perforations (NS). When the probe was covered by a glove, one instance of visible contamination
occurred (0.78%, 95% C.I. 0–1.6%) compared with eight instances when the probe was covered with
a condom (7.8%, 95% C.I. 5.2–10.4%, P < .007). The prevalance of preexisting defects in the 50
unused gloves was 2%, which is not significantly different from the prevalence in used gloves. There
were no defects in the 50 unused condoms compared with 7 in the used condoms (P = .057). Visible
contamination of the endovaginal probe with blood or genital tract secretions is more likely when
condoms are used as sheaths. However, even gloves provide imperfect coverage of the probe,
illustrating the need for thorough decontamination of the endovaginal instrument after each use.