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The effect of preheated versus room-temperature skin disinfection on bacterial colonization during pacemaker device implantation: a randomized controlled non-inferiority trial

Abstract

Background

In clinical practice, patients who are awake often comment that cold surgical skin disinfectant is unpleasant. This is not only a problem of patients’ experience; heat loss during the disinfection process is a problem that can result in hypothermia. Evidence for the efficacy of preheated disinfection is scarce.

We tested whether preheated skin disinfectant was non-inferior to room-temperature skin disinfectant on reducing bacterial colonization during pacemaker implantation.

Methods

This randomized, controlled, non-inferiority trial included 220 patients allocated to skin disinfection with preheated (36 °C) or room-temperature (20 °C) chlorhexidine solution in 70 % ethanol. Cultures were obtained by swabbing at 4 time-points; 1) before skin disinfection (skin surface), 2) after skin disinfection (skin surface), 3) after the incision (subcutaneously in the wound), and 4) before suturing (subcutaneously in the wound).

Results

The absolute difference in growth between patients treated with preheated versus room-temperature skin disinfectant was zero (90 % CI −0.101 to 0.101; preheated: 30 of 105 [28.6 %] vs. room-temperature: 32 of 112 [28.6 %]). The pre-specified margin for statistical non-inferiority in the protocol was set at 10 % for the preheated disinfectant. There were no significant differences between groups regarding SSIs three month postoperatively, which occurred in 0.9 % (1 of 108) treated with preheated and 1.8 % (2 of 112) treated with room-temperature skin disinfectant.

Conclusion

Preheated skin disinfection is non-inferior to room-temperature disinfection in bacterial reduction. We therefore suggest that preheated skin disinfection become routine in clean surgery.

Trial registration

The study is registered at ClinicalTrials.gov (NCTO2260479).

Background

Health-care-associated infections are a global concern for patient safety [1, 2]. With emerging antibiotic resistance, it is important to find safe preventive measures [35].

During clean surgery, such as pacemaker implantation, surgical site infections (SSIs) are a rare (1–1.25 %) but serious complication [68]. Pathogens isolated from SSIs are mainly staphylococci, both Staphylococcus aureus and coagulase-negative staphylococci, and streptococci [1, 4, 9]. Studies have shown that reducing the number of contaminating bacteria can prevent SSIs [10, 11]. Bacteria causing SSIs originate from the patient or the surgical team [12, 13].

Skin disinfection reduces the number of bacteria, thereby reducing SSIs [1]. According to the Cochrane Collaboration, there is insufficient research regarding the effects of skin disinfection [14]. In clinical practice, patients comment on the chill they experience during skin disinfection prior to surgery. This is not only a problem of patients’ comfort; heat loss during the disinfection procedure can cause hypothermia [15]. Hypothermia causes complications including myocardial events, SSIs, coagulopathy, and prolonged hospitalization [16, 17]. A pilot study showed that preheated disinfectant seemed to be comparable to room-temperature disinfectant in reducing bacterial growth [18]. To our knowledge there are no other studies reported that have examined the effectiveness of preheated skin disinfectant on bacterial colonization or SSIs.

The primary aim of this study was to test if preheated (36 °C) skin disinfectant is non-inferior to room-temperature (20 °C) skin disinfectant regarding skin colonization. The secondary aim was to investigate whether gender had an impact on differences in bacterial colonization in the surgical wound or SSIs among patients undergoing surgery.

Methods

Study design and participants

This study was a randomized, controlled, non-inferiority trial that included 220 patients undergoing pacemaker, implantable cardioverter-defibrillator, or cardiac resynchronization therapy under local anaesthesia. The study was performed at a cardiothoracic and vascular surgery department in Sweden. Inclusion criteria were age 18 years or older and ability to read and understand Swedish. Exclusion criteria were infection in an existing implanted device. The Regional Ethical Review Board of Uppsala approved the study (reference number 2012/255). Written informed consent was obtained.

Intervention and randomization

Patients were included consecutively after arriving in the operating room (OR). Enrolment to the operation was done by an external controller who had no knowledge of the present study. Patients were randomly allocated to skin disinfectant solution (chlorhexidine 5 mg/mL in 70 % ethanol, Fresenius Kabi AS, Halden, Norway) that was preheated or at room temperature. Allocation took place directly after patients provided informed consent. Patients were stratified by gender and randomly allocated based on a computer-generated randomization list made by an independent statistician. The patient and the laboratory technician that performed the analysis were blinded to the allocation.

Data collection

Patients showered twice with Descutan®, a 4 % chlorhexidine soap (Fresenius Kabi AB, Uppsala, Sweden), prior to surgery. Most patients received elective surgery and arrived at the hospital on the morning of surgery. Following standard procedures, intravenously administered antibiotic prophylaxis (cloxacillin 2 g) was given in the ward 15–30 min prior to surgery. The operating room had an average temperature of 19 °C with upward displacement ventilation. Sterile disposable surgical gowns and indicator gloves were worn by the OR team. Participants underwent skin disinfection during 2 min. The skin disinfectant was stored at room-temperature and kept at 20 °C, while the preheated skin disinfectant was stored in a warming cupboard and kept at 36 °C. The manufacturer provided a written statement that the bottles could be stored in a warming cupboard at temperatures up to 40 °C for 7 days without changing the compound.

The participants were disinfected from the cheek down and over the sternum according to routine procedures. Sterile draping was for single use only. Cultures were obtained at four time-points using a nylon-flocked swab (ESwab, COPAN Italia S.p.A., via Perotti 10, Brescia, Italy); 1) before skin disinfection on the skin surface, 2) after skin disinfection on the skin surface, 3) directly after the incision (subcutaneously in the wound), and 4) before closing with sutures (subcutaneously in the wound). Swabs for cultures were moistened with saline then rubbed for 15 s on the skin surface (incision site, approximately 10 mm × 50 mm). Swabs taken in the wounds were rubbed along the inside of the incision and along the edges for 15 s with a dry swab. Surgery was performed by a cardiologist. Cultures were kept cold until their arrival at the laboratory then analysed according to a specific study protocol.

The swabs were vortexed for a few seconds and 50 μl aliquots of the liquor transportation media was subcultured in hematin agar medium 4.3 % (w/v) (Columbia Blood Agar Base, Acumedia Neogen Corporation, Lansing, MI, USA) supplemented with 6 % (v/v) chocolatized defibrinated horse blood and incubated at 36 °C under aerobic conditions.. Samples were also subcultured on FAA plates (LAB 90 Fastidious Anaerobe Agar 4.6 % [w/v]; LAB M Ltd., Lancashire, UK) supplemented with 5 % (v/v) defibrinated horse blood and incubated under anaerobic conditions (10 % H2, 10 % CO2, 80 % N2) at 37 °C for 5 days. After 24 and 48 h of incubation under aerobic conditions or 5 days under anaerobic conditions, bacterial growth was determined quantitatively (colony forming units [cfu]/mL). Culture diagnostics and species verification were performed based on characteristic colony morphology, and using routine diagnostic procedures.

Patient follow-up

After surgery, all patients were followed-up for three months to detect SSIs, which were defined according to the United States Centers for Disease Control and Prevention (CDC) criteria for SSI [1].

Statistical analyses

Analyses were performed using SPSS, version 22. The primary outcome was based on a non-inferiority hypothesis, and the sample size was guided by an earlier study [18]. A sample size of 102 participants per group provided 80 % power at a one-sided significance level of 5 % with an expected proportion of bacterial growth of 0.09 and the maximal allowable difference of 0.10 non-inferiority limit, which means that a proportional difference of no more than 0.10 in favour of the pre-heated disinfectant was accepted as non-inferiority. To cover potential missing data, the sample size was increased by 16 participants for a total of 220 participants divided into two groups. Due to a non-inferiority hypothesis, the absolute difference of the primary outcome was supplemented with a two-sided 90 % confidence interval (CI); otherwise, a regular two-sided 95 % significance level of 5 % was used.

Bacterial counts and other non-normally distributed variables were analysed with the Mann–Whitney U test and normally distributed variables with an unpaired t-test. Categorical variables were evaluated with χ 2 -test or Fisher’s exact test as appropriate.

Results

Recruitment

Between January 2013 and November 2014, 220 patients receiving pacemakers were enrolled and randomly allocated to receive skin disinfectant that was preheated (n = 108) or at room-temperature (n = 112). Patients were followed for three months after surgery (Fig. 1). Characteristics that are known risk factors affecting SSIs are; diabetes, eczema, age and others (Table 1).

Fig. 1
figure 1

Flow chart

Table 1 Patients baseline characteristics and surgical factors

Bacterial growth

One hundred and one of 106 (95.3 %) skin cultures taken before receipt of preheated skin disinfectant showed growth compared with 108 of 112 (96.4 %) taken before receipt of room temperature disinfectant. Thirty of 105 (28.6 %) skin cultures after receipt of preheated skin disinfectant showed growth compared with 32 of 112 (28.6 %) receiving room-temperature skin disinfectant. The absolute difference in growth was zero (90 % CI −10.1 to 10.1) (Table 2). Microorganisms identified before skin disinfection included Propionibacterium acnes, coagulase-negative staphylococci (CoNS), alpha-haemolytic streptococci, anaerobic diphtheriod rods, Bacillus species, Micrococcus species, Staphylococcus aureus, anaerobic gram-positive cocci, Proteus species, and Rothia mucilaginosa. At subsequent time points, the amount of different bacteria and the number of bacteria changed (Fig. 2). The most frequently identified pathogen after skin disinfection both on the skin and in the wound was P. acnes followed by CoNS (Table 3). No significant differences were observed in any of the cultures at the 4 time-points regarding growth or median or mean cfu/mL between the groups (Table 4).

Table 2 Bacterial growth at the four time points
Fig. 2
figure 2

Bacterial growth before and after skin disinfectant. Bacterial growth before and after treatment with skin disinfectant (chlorhexidine 5 mg/mL in 70 % ethanol) at the four time points. The median is identified by a line inside the box. The length of the box is the interquartile range (IQR), and whiskers are min and max if no outliers are present. Outliers of more than 1.5 IQR’s are labeled as (o) and outliers of more than three IQR are labelled as (*)

Table 3 Species of bacteria identified
Table 4 Mean bacterial growth

Gender

Cultures showed that males had significantly more bacteria at the four time-points than females irrespectively of the temperature of the skin disinfectant. Gender differences at the first time-point appeared in both the preheated (p = 0.011) and room-temperature disinfectant groups (p = 0.037). A gender difference was also seen during the second, third, and fourth time-point (p ≤ 0.001). Analyses performed on the overall group or with males and females separately showed no significant differences regarding disinfection with preheated or room-temperature disinfectant (Table 4).

Surgical site infections

There were no significant differences in SSIs three months postoperatively between patients who received preheated versus room temperature skin disinfectant; 1 (female) of 108 (0.9 %) vs 2 (1 male and 1 female) of 112 (1.8 %), respectively. At the time of surgery, samples from females showed growth only before skin disinfection, whereas the male displayed growth of P. acnes at all four time-points and CoNS at the first and last time points. Cultures taken postoperatively, when patients were diagnosed for SSI, were negative for both female patients, whereas the cultures from the male patient were positive for S. aureus, CoNS, P. acnes, and beta-haemolytic streptococci group G.

Discussion

Bacterial growth

In this study, no significant differences were found related to the presence of bacteria, confirming that preheated and room-temperature skin disinfectant have similar bactericidal effects, as shown in our previous pilot study [18]. The results clearly show that preheated or room temperature skin disinfectant reduce the number of bacteria on the skin and prevent SSIs equally well. The most frequently identified bacteria in the wound after disinfection was P. acnes, which also inhabits deeper layers of the skin [19, 20]. A possible explanation is that when the incision is made, deeper layers of the skin are exposed and P. acnes relocate into the wound [20]. P. acnes can be a causative factor of SSIs [2023].

Gender

Earlier studies have shown that the amount of bacteria differs between males and females and this study supports that finding [12, 24]. The effectiveness of preheated or room-temperature skin disinfectant was equivalent.

Surgical site infections

The male patient who experienced SSI showed growth in cultures taken at all four time-points. Two other species of bacteria, S. aureus and beta-haemolytic streptococci group G, were also found when the SSI was diagnosed. These species were not present at the time of surgery. Cultures taken postoperatively to determine the causative pathogens were negative in the female patients with SSIs. According to the criteria, SSI could be diagnosed as purulent drainage, fever, tenderness, and usually a positive culture or diagnosed as SSI by the attending physician [1]. The reason these cultures did not show any growth could possibly be due to an ability of the bacteria to protect themselves with biofilm [19], but also because P. acnes has a slow-growing nature [23].

Limitations

There are limitations to this study. First, this study had a power problem related to the population size because the power calculation was made based on 10 % growth, whereas in the present study the patients showed 28.6 % bacterial growth after skin disinfection. Secondly, this study was designed as a non-inferiority trial to detect differences in bacterial contamination, not to detect differences in SSIs.

In conclusion, recommendations aimed at preventing SSIs should be evidence based [25]. The assumption that preheated skin disinfection is non-inferior to room-temperature disinfectant in bacterial reduction appears to be correct. We therefore suggest that preheated skin disinfection can be used routinely prior to clean surgery. Additional studies involving other types of surgery, including those affecting other body sites and levels of complexity and length, are warranted.

References

  1. Mangram AJ, Horan TC, Pearson ML, Silver LC, Jarvis WR. Guideline for prevention of surgical site infection, 1999. Hospital Infection Control Practices Advisory Committee. Infect Control Hosp Epidemiol. 1999;20(4):250–78. quiz 79–80.

    Article  CAS  PubMed  Google Scholar 

  2. World Health Organization. Report on the burden of endemic health care-associated infection worldwide. Geneva: WHO; 2011.

    Google Scholar 

  3. de Lastours V, Chau F, Tubach F, Pasquet B, Ruppe E, Fantin B. Independent behavior of commensal flora for carriage of fluoroquinolone-resistant bacteria in patients at admission. Antimicrob Agents Chemother. 2010;54(12):5193–200.

    Article  PubMed Central  PubMed  Google Scholar 

  4. Greenspon AJ, Rhim ES, Mark G, Desimone J, Ho RT. Lead-associated endocarditis: the important role of methicillin-resistant Staphylococcus aureus. Pacing Clin Electrophysiol. 2008;31(5):548–53.

    Article  PubMed  Google Scholar 

  5. den Heijer CD, van Bijnen EM, Paget WJ, Pringle M, Goossens H, Bruggeman CA, et al. Prevalence and resistance of commensal Staphylococcus aureus, including meticillin-resistant S aureus, in nine European countries: a cross-sectional study. Lancet Infect Dis. 2013;13(5):409–15.

    Article  Google Scholar 

  6. Margey R, McCann H, Blake G, Keelan E, Galvin J, Lynch M, et al. Contemporary management of and outcomes from cardiac device related infections. Europace. 2010;12(1):64–70.

    Article  PubMed  Google Scholar 

  7. Nery PB, Fernandes R, Nair GM, Sumner GL, Ribas CS, Menon SM, et al. Device-related infection among patients with pacemakers and implantable defibrillators: incidence, risk factors, and consequences. J Cardiovasc Electrophysiol. 2010;21(7):786–90.

    PubMed  Google Scholar 

  8. Reynolds MR, Cohen DJ, Kugelmass AD, Brown PP, Becker ER, Culler SD, et al. The frequency and incremental cost of major complications among medicare beneficiaries receiving implantable cardioverter-defibrillators. J Am Coll Cardiol. 2006;47(12):2493–7.

    Article  PubMed Central  PubMed  Google Scholar 

  9. Chu VH, Crosslin DR, Friedman JY, Reed SD, Cabell CH, Griffiths RI, et al. Staphylococcus aureus bacteremia in patients with prosthetic devices: costs and outcomes. Am J Med. 2005;118(12):1416.

    Article  PubMed  Google Scholar 

  10. Twum-Danso K, Grant C, al-Suleiman SA, Abdel-Khader S, al-Awami MS, al-Breiki H, et al. Microbiology of postoperative wound infection: a prospective study of 1770 wounds. J Hosp Infect. 1992;21(1):29–37.

    Article  CAS  PubMed  Google Scholar 

  11. Houang ET, Ahmet Z. Intraoperative wound contamination during abdominal hysterectomy. J Hosp Infect. 1991;19(3):181–9.

    Article  CAS  PubMed  Google Scholar 

  12. Kuhme T, Isaksson B, Dahlin LG. Wound contamination in cardiac surgery. A systematic quantitative and qualitative study of the bacterial growth in sternal wounds in cardiac surgery patients. APMIS. 2007;115(9):1001–7.

    Article  PubMed  Google Scholar 

  13. Bitkover CY, Marcusson E, Ransjo U. Spread of coagulase-negative staphylococci during cardiac operations in a modern operating room. Ann Thorac Surg. 2000;69(4):1110–5.

    Article  CAS  PubMed  Google Scholar 

  14. Dumville JC, McFarlane E, Edwards P, Lipp A, Holmes A. Preoperative skin antiseptics for preventing surgical wound infections after clean surgery. Cochrane Database Syst Rev. 2013;3:CD003949.

    PubMed  Google Scholar 

  15. Sessler DI, Sessler AM, Hudson S, Moayeri A. Heat loss during surgical skin preparation. Anesthesiology. 1993;78(6):1055–64.

    Article  CAS  PubMed  Google Scholar 

  16. Pikus E, Hooper VD. Postoperative rewarming: are there alternatives to warm hospital blankets. J Perianesth Nurs. 2010;25(1):11–23.

    Article  PubMed  Google Scholar 

  17. Insler SR, Sessler DI. Perioperative thermoregulation and temperature monitoring. Anesthesiol Clin. 2006;24(4):823–37.

    Article  PubMed  Google Scholar 

  18. Wistrand C, Nilsson U. Effects and experiences of warm versus cold skin disinfection. Br J Nurs. 2011;20(3):148. 50-1.

    Article  PubMed  Google Scholar 

  19. Jahns AC, Alexeyev OA. Three dimensional distribution of Propionibacterium acnes biofilms in human skin. Exp Dermatol. 2014;23(9):687–9.

    Article  PubMed  Google Scholar 

  20. Lee MJ, Pottinger PS, Butler-Wu S, Bumgarner RE, Russ SM, Matsen 3rd FA. Propionibacterium persists in the skin despite standard surgical preparation. J Bone Joint Surg Am. 2014;96(17):1447–50.

    Article  PubMed  Google Scholar 

  21. Kurz M, Kaufmann BA, Baddour LM, Widmer AF. Propionibacterium acnes prosthetic valve endocarditis with abscess formation: a case report. BMC Infect Dis. 2014;14:105.

    Article  PubMed Central  PubMed  Google Scholar 

  22. Aleissa S, Parsons D, Grant J, Harder J, Howard J. Deep wound infection following pediatric scoliosis surgery: incidence and analysis of risk factors. Can J Surg. 2011;54(4):263–9.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Chung S, Kim JS, Seo SW, Ra EK, Joo SI, Kim SY, et al. A case of brain abscess caused by Propionibacterium acnes 13 months after neurosurgery and confirmed by 16S rRNA gene sequencing. Korean J Lab Med. 2011;31(2):122–6.

    Article  PubMed Central  PubMed  Google Scholar 

  24. Falk-Brynhildsen K, Soderquist B, Friberg O, Nilsson UG. Bacterial recolonization of the skin and wound contamination during cardiac surgery: a randomized controlled trial of the use of plastic adhesive drape compared with bare skin. J Hosp Infect. 2013;84(2):151–8.

    Article  CAS  PubMed  Google Scholar 

  25. Liau KH, Aung KT, Chua N, Ho CK, Chan CY, Kow A, et al. Outcome of a strategy to reduce surgical site infection in a tertiary-care hospital. Surg Infect (Larchmt). 2010;11(2):151–9.

    Article  Google Scholar 

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Acknowledgements

We wish to express our gratitude to all who were involved in the operating department and the department of laboratory medicine, Clinical Microbiology. We thank Tommy Andersson, Peter Lindell, who performed all surgery, and Bengt Hellmark, who contributed everything that was needed at the department of laboratory medicine.

Role of the funding source

This study was funded by Örebro County Council Research Committee, Örebro, Sweden and Örebro University.

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Corresponding author

Correspondence to Camilla Wistrand.

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Competing interests

B. Söderquist has been a consultant for Pfizer and Janssen-Cilag. Otherwise, the authors have no financial, personal, or other relationship that could be viewed as presenting a potential conflict of interests.

Authors’ contributions

All named authors have seen and agreed to the submitted version of the paper as well as those included inthe acknowledgements section. CW was the main author. BS and UN supervised the writing and was also involved in the planing of the manuscript. BS was responsible for the protocol and the departement of microbiology. AM aided with statistics. BS has been a consultant for Pfizer and Janssen-Cilag. All authors read and approved the final manuscript.

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Wistrand, C., Söderquist, B., Magnusson, A. et al. The effect of preheated versus room-temperature skin disinfection on bacterial colonization during pacemaker device implantation: a randomized controlled non-inferiority trial. Antimicrob Resist Infect Control 4, 44 (2015). https://doi.org/10.1186/s13756-015-0084-1

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