Optimal Timing of Preoperative Skin Preparation with Povidone-Iodine for Spine Surgery: A Prospective, Randomized Controlled Study

Article information

Asian Spine J. 2015;9(3):423-426
Publication date (electronic) : 2015 June 08
doi : https://doi.org/10.4184/asj.2015.9.3.423
Department of Orthopaedic Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Corresponding author: Tatsuya Yasuda. Department of Orthopaedic Surgery, Hamamatsu University of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu 431-3192, Japan. Tel: +81-53-435-2299, Fax: +81-53-435-2296, t.yasuda@hama-med.ac.jp
Received 2014 October 08; Revised 2014 November 18; Accepted 2014 November 25.

Abstract

Study Design

A prospective, randomized, controlled study.

Purpose

The objective of this study was to evaluate the effectiveness of two techniques of skin preparation with povidone-iodine.

Overview of Literature

Preoperative skin preparation is important for preventing surgical site infection by reducing the bacteria in the surgical area. Povidone-iodine is a commonly used agent for preoperative skin preparation, and further decrease in surgical site infections can be expected by understanding how to apply it more effectively.

Methods

Eighty-nine spine surgery patients were randomly allocated to two groups. In group A, povidone-iodine was applied to the surgical site just before starting the operation; in group B, povidone-iodine was applied several minutes prior to starting the operation and was allowed to dry. We collected samples from the wound edge before suturing, and we compared the rates of positive culture between the two groups.

Results

The rate of positive culture was 30.2% (13 out of 43 patients) in group A, and 6.5% (3 out of 46 patients) in group B. This indicates that there was a significant difference in postoperative infection rates between group A and group B.

Conclusions

Because bacteria on the skin appeared significantly reduced by allowing povidone-iodine to dry for several minutes prior to surgery, we recommend this approach to reduce the incidence of postoperative infections.

Introduction

Surgical site infection (SSI) is a common complication after spinal surgery. Despite the use of prophylactic antibiotics, advances in surgical techniques and postoperative care, clinical results of compromised patients show significant morbidity and prolonged hospitalization.

Recently, the surgical indication has been expanded to elderly patients, who are considered to be having a relatively higher risk of surgical infection. Additionally, patients with diabetes and who are on dialysis are at high risk of infection due to immunocompromised status.

The stage of prevention of surgical site infection can be classified in three phases; preoperative, intraoperative, and postoperative. Skin preparation in the preoperative phase is very important for preventing infection, and povidone-iodine is one of the most commonly used agents for this purpose. This study investigated the effectiveness of two different timings of skin preparation with povidone-iodine.

Materials and Methods

In this prospective study, 89 consecutive patients scheduled for spinal surgery between March 2010 and September, 2010 were randomly allocated to 2 groups according to the patient identification numbers with their consent. Forty-three patients were included in group A and 46 patients were included in group B. The average patient age was 61.9 years in group A (range, 18-86 years) and 58.1 years in group B (range, 14-82 years). The average operating time was 230 minutes in group A and 216 minutes in group B, respectively. Cervical surgery was performed in 17 patients (39.5%) of group A and 15 patients (32.6%) of group B. Instrumentation surgery was performed in 25 patients (58.1%) of group A and 24 patients (52.2%) of group B (Table 1).

Table 1

Patient demographics in each group

In group A, povidone-iodine was applied to the surgical site just before the skin incision, after the surgeon's hands were scrubbed. In group B, povidone-iodine was applied before the surgeon's hands were scrubbed. Therefore, there was an interval of at least five minutes, enough time for drying povidone-iodine, before skin incision compared to povidone-iodine application in group A. In all cases, the surgical field was sealed with an antimicrobial plastic adhesive wound drape just before starting the surgery.

Culture samples were collected by rubbing a cotton swab at the wound edge just before wound closure and then they were incubated at 37℃ for 5 to 7 days. Bacteria were identified by means of standard laboratory identification methods.

Cefazolin was administered three times on the day of surgery, before surgery, one hour after surgery, and six hours after surgery, and two times on the next day as a prophylactic antibiotic.

We analyzed the rate of positive bacterial culture in each group. Pearson's χ2 tests were used to compare the positive culture rate between the two groups. The level of significance was set at p<0.01.

Results

The positive culture rate was 30.2% (13 out of 43 patients) in group A and 6.5% (3 out of 46 patients) in group B (Table 2), and it was significantly different between group A and group B (p=0.004). In group A, coagulase negative Staphylococcus was identified in 12 cultures and methicillin-sensitive Staphylococcus aureus was identified in 1 culture. In group B, three different bacteria (γStreptococcus, staphylococcus epidermidis, and coagulase negative Staphylococcus) were identified in the culture, respectively (Table 3). Two cases of SSI (deep infection) (2 out of 46 patients, 4.3%) were identified in group B four weeks after surgery, and cultures from the wound edge intraoperatively were negative. There was no case of SSI in group A after the surgery.

Table 2

Culture results

Table 3

Bacterial species

Discussion

SSI following adult spinal surgery is a common complication that has been reported to occur in 0.7% to 12.0% [12345678910] of patients, and it results in higher postoperative morbidity, mortality, and increased health care costs [11112]. Recently, the surgical indication has been expanded to elderly patients; hence, the chances of spinal surgery in immunocompromised patients have increased. In particular, cases of spinal instrumentation surgery are comparatively difficult to treat when they get infected [13]; thus, prevention of infection is very important for spinal surgery.

The prevention of SSI can be classified into the preoperative, intraoperative, and postoperative phases. The preoperative phase includes diabetes control, shorter hospital stay before surgery, etc. Also, it is important to check the preoperative colonization status, for example, the history of dental treatment. Techniques for prevention of SSI during the operation commonly include the use of a clean room, appropriate antibiotic use, and maintenance of clean surgical fields. Finally, good nutrition and proper wound care are important factors in postoperative prevention of SSI. In this study, the two cases of SSI (deep infection) found in group B were of postoperative phase infections since they occurred four weeks after surgery, and the cultures from the wound edge intraoperatively were negative.

Preoperative skin preparation is necessary for the prevention of SSI in the intraoperative phase. In the intraoperative phase, a key factor for preventing infection is the elimination of bacterial contamination of the surgical site at the time of surgery [1415161718]. The purpose of preoperative skin preparation is to reduce bacteria on the skin. In this study, the positive culture rate in group A was significantly higher than that in group B. Thus, the method used in group B was more effective in the intraoperative phase.

Although variation exists in timings and techniques for skin preparation before surgery, one of the most commonly used techniques involves painting the surgical field with povidone-iodine [1213141516]. Povidone-iodine is a bactericidal agent effective against a wide spectrum of pathogens. The preventive effect of povidone-iodine on SSI has been reported to be equivalent to that of other antiseptic agents [24]. Moen et al. [13] reported the number of bacterial colonies after spraying povidone-iodine 1 minute before and 3 minutes before performing abdominal wall surgery. They reported that spraying povidone-iodine 3 minutes before was more effective in reducing bacterial counts than spraying povidone-iodine 1 minute before surgery. Additionally, the results of this study suggested that povidone-iodine was more effective when it was allowed to dry for 10 minutes prior to surgery. Additionally, if the drape was used in a wet condition, it was possible that the effect of the shield was insufficient. We recommend allowing 10 minutes drying time after povidone-iodine painting of the surgical field for preoperative preparation.

A limitation of this study is that only analysis of cultures from the wound edge was conducted. Also, the plastic adhesive wound drape was peeled easily in group A since the surgical field was not dry when it was applied. Plastic shielding may have also been associated with culture results. Another limitation is the lack of patient background data, especially the risk factors for infection. Nevertheless, the purpose of preoperative skin preparation is to reduce bacteria in the surgical field and to reduce the incidence of SSI. Therefore, allowing 10 minutes drying time after povidone-iodine painting of the surgical field is a simple step in preoperative skin preparation that may reduce the rate of SSI, thus resulting in reducing length of the hospital stay and costs incurred by the patient.

Conclusions

We evaluated the effectiveness of two techniques of skin preparation with povidone-iodine. Because bacteria on the skin appeared significantly reduced by allowing povidone-iodine to dry for 10 minutes prior to surgery, we recommend this approach to reduce the incidence of postoperative infections.

Notes

Conflict of Interest: No potential conflict of interest relevant to this article was reported.

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Article information Continued

Table 1

Patient demographics in each group

Table 1

Table 2

Culture results

Table 2

p=0.004.

Table 3

Bacterial species

Table 3