Surgical Glove Perforation C-Section & Surgical Site Infections
glove Micro-Perforation and Surgical Site Infection Risk After Cesarean Section: A Single-Center Observational Study
Table of Contents
Abstract
Background: Cesarean section (CS) is a common surgical procedure associated with a significant risk of surgical site infection (SSI). Maintaining surgical sterility is paramount, yet glove perforation, even microscopic, can compromise this. This study investigated the association between glove micro-perforation and superficial SSI rates following elective cesarean sections.
Methods: This single-center,observational study compared SSI rates in 537 patients undergoing elective cesarean section: 32 with documented glove micro-perforation and 505 in a control group without observed perforation. Exclusion criteria included pre-existing inflammatory conditions, multiple pregnancies, ASA class III or higher, midline incision, allergies to study materials, and loss to follow-up. Superficial SSI rates were the primary outcome. Statistical analysis included Mann-Whitney U tests, chi-square tests, Fisher’s exact tests, and multivariable logistic regression.
Results: The glove perforation group exhibited a substantially higher rate of superficial SSI (31.25%) compared to the control group (6.93%) (p < 0.001). multivariable logistic regression confirmed an independent association between glove micro-perforation and SSI, even after adjusting for confounding factors such as emergency CS, diabetes mellitus, obesity, surgical duration, and intraoperative blood loss. A post-hoc power analysis demonstrated sufficient statistical sensitivity (power > 99.9%).
Conclusion: Glove micro-perforation is independently associated with a substantially increased risk of superficial SSI following elective cesarean section. These findings underscore the critical importance of meticulous surgical technique,vigilant monitoring for glove integrity,and consideration of alternative glove options to minimize perforation risk.
Introduction
cesarean section (CS) rates have been steadily increasing globally, including in Turkey [1]. While CS can be life-saving, it is a major surgical intervention associated with higher morbidity compared to vaginal delivery, with surgical site infection (SSI) being a significant concern [2]. SSI not only prolongs hospital stays and increases healthcare costs but also poses serious risks to maternal health, including wound dehiscence, sepsis, and even mortality [3].
Maintaining a sterile surgical field is basic to preventing SSI. However, breaches in sterile technique, even seemingly minor ones, can introduce pathogens and lead to infection. Glove perforation, whether visible or microscopic, represents a potential pathway for microbial contamination [4]. Despite advancements in glove technology, perforation remains a recognized risk during surgical procedures [5].The true incidence of glove perforation is highly likely underestimated, as micro-perforations frequently enough go undetected [6]. Recent research highlights the need for a deeper understanding of the relationship between glove integrity and SSI rates, notably in the context of CS. This study aimed to investigate the association between documented glove micro-perforation and the incidence of superficial SSI following elective cesarean sections in a single center. Understanding this relationship is crucial for developing targeted strategies to reduce SSI rates and improve maternal outcomes. The increasing CS rates in Turkey [1] necessitate a focused approach to minimizing post-operative complications like SSI.
Methods
Study Design and setting
This was a single-center, observational study conducted at [Hospital Name Redacted for Privacy] between [Start Date Redacted] and [End Date Redacted]. The study was approved by the institution’s ethics committee and conducted in accordance with the declaration of Helsinki. All patients provided written informed consent prior to participation.
Participants
Patients undergoing elective cesarean section were eligible for inclusion. Exclusion criteria were: (1) lack of informed consent, (2) a history of inflammatory disease or clinical chorioamnionitis, (3) multiple pregnancies, (4) american Society of Anesthesiologists (ASA) physical status classification of III or higher, (5) undergoing midline skin incision, (6) known allergies to chlorhexidine, antibiotics, or latex, and (7) loss to follow-up during the study period.
Exposure and Outcome
The primary exposure was documented glove micro-perforation identified during the surgical procedure. Perforation was identified visually by the surgical team.The primary outcome was the advancement of a superficial SSI, defined according to the Centers for Disease Control and Prevention (CDC) national Healthcare Safety Network (NHSN) criteria [7]. Superficial SSI was characterized by redness, swelling, and drainage within 30 days post-operatively. Deep incision or organ/space infections were specifically excluded from the analysis, as thay did not occur in either study group.
Sample Size Calculation
A priori sample size calculation was performed using G*Power version 3.1.9.7
