Methods: We included 100 consecutive CABG patients in a double-blind and placebo controlled study. Patients were randomized into two groups as gentamicin and placebo groups. During surgery, gentamicin/isotonic solution absorbed sponges were placed beneath the edges of the sternum-retractor. Primary end points were the development of SWI, wound revision, and mortality within the first 30 days after CABG. Two groups were compared statistically.
Results: Sternal wound infection developed in six patients. The impact in three patients was superficial, and no wound revision was required. In the other three patients, both cutaneous and subcutaneous layers of the skin were involved, and they all needed revision. All SWI cases were in the placebo group, and there was a significant difference between the groups (p=0.027). No mortality was observed in any patient.
Conclusion: The statistical comparison between gentamicin and placebo groups showed a significant difference. This result revealed that local use of gentamicin-sponges can be at least as effective as the use of gentamicin-collagen implants. Therefore, placing gentamicin-soaked sponges beneath the sternum-retractor during CABG can be beneficial to decrease SWI rates.
The major risk factors that affect the incidence of SWI are diabetes mellitus (DM), obesity, technical errors in sternal wiring, and early revision, but the use of the bilateral internal thoracic artery as well as renal failure, smoking, male gender, low left ventricular ejection fraction (LVEF), and prolonged length of intensive care unit (ICU) stay can also be found.[7] Currently, more complex and redo operations are being performed on a daily basis.[1] Although prophylactic antibiotics are routinely used, SWI remains a leading factor that affects morbidity and mortality rates among cardiac surgery patients.[1,5,8] If mediastinitis, the most advanced form of SWI, is included in the figures, the mortality rate increases markedly to as high as 50%.[9] In addition, this most severe form of SWI also decreases the long-term survival rates after open heart surgery.[10] For all of these reasons, additional methods of treatment are needed for SWIs.[1] Besides controlling risk factors and using systemic antibiotics, previous studies have tested the efficacy of nasal antibiotics to counteract SWIs with the goal of eradicating methicillin-resistant Staphylococcus aureus (MRSA).
Previous studies have also investigated the effects of topical antibiotics (e.g., vancomycin and gentamicin) on the frequency of SWIs after heart surgery.[11,12] Recent studies have also used gentamicin-impregnated collagen implants while closing the sternum to reduce the frequency of mediastinitis, and locally administered prophylactic antibiotics have been widely used for soft tissue and bone infections. In addition, they have been utilized during surgery as well.[2,13] Moreover, a previous study reported a significant decrease in the frequency of mediastinitis after the use of local gentamicin-collagen implants.[14] After these reports, multiple studies and a recent meta-analysis were then carried out which have confirmed the possible positive effects of locally administered gentamicin in cardiac surgery.[1,2,5] Undergoing surgical procedures with topical local gentamicin also decreases the incidence of postoperative infection, and this served as the starting point of this study.[15] Our aim was to investigate whether the use of gentamicin-soaked sponges during coronary artery bypass graft surgery (CABG) had a protective effect on SWI.
Figure 1: Flow chart of the study.
An independent nurse prepared the gentamicin/ placebo solutions. The applied solvent for the gentamicin group (group 1) included a total of 320 mg of gentamicin in 250 ml of an isotonic solution while the solvent for the placebo group (group 2) contained 250 ml of a saline solution. During surgery, we placed the solution-absorbed sponges beneath the edges of the sternum retractor, and these were in contact with all layers of the skin, subcutaneous tissues, and both sides of the sternum (Figure 2). If the sponges needed to be replaced, new ones were inserted. The sponges were applied from the very beginning of the procedure after the sternotomy and were not withdrawn until the retractor was removed.
Figure 2: Cross-sectional view of the surgical site.
Intravenous prophylactic antibiotics were given to all of the patients, with cefazolin being administered to 98 patients (98%) and vancomycin to two patients (2%) with a beta (b)-lactam antibiotic allergy. The patients were followed up while they were in the intensive care unit (ICU) as well as during the entire hospitalization process and for three months postoperatively.
All of the operations were performed by the same surgical team using on-pump CABG. Mild hypothermia was attained using a body temperature of 32 °C in all patients, and myocardial protection was achieved via both antegrade and retrograde cold blood cardioplegia. Proximal and distal anastomoses was performed using a cross-clamp, and left internal mammary artery-left anterior descending coronary artery (LIMA-LAD) anastomosis was utilized for all of the patients.
We accepted the development of SWI, wound revision, and mortality within the first 30 days after CABG as the primary end points of the study, and the secondary end points included other morbidity factors such as postoperative renal functions, revision rates, and length of hospital stay.
Statistical analysis
All categorized variables were presented as
numbers and percentages (n, %), and all numerical
variables were expressed as mean ± standard
deviation (SD). Ordinal variables were expressed
as mean ± SD with median values. In addition, we
compared the parametric continuous variables using
Student’s T-test and the non-parametric variables
via the Mann-Whitney U test. Furthermore, a chisquare
or Fisher’s exact test were used to compare
the categorical variables. The statistical power of the
study was represented by the presence of SWI, and
this was calculated as 92.2% [for an alpha (a) error
level of 5%]. The percentage of patients with SWI in
groups 1 and 2 (50 patients each) was 0% (accepted as
<1%) and 12%, respectively.
Table 1: Preoperative variables
Table 3: Intraoperative variables
Table 4: Postoperative variables
Sternal wound infection occurred in six patients. Three of these were type A and three were type B, but none had type C SWI (Table 5). Moreover, all of the SWI patients were in group 2, and there was a statistically significant difference between the two groups (p=0.027) (Table 6). Wound revisions were needed in all three patients with type B SWI. Furthermore, the groups had similar saphenous vein harvesting site infection rates (Table 6). No mortality was detected among the patients in our study.
Table 5: “Centers for Disease Control” classification of sternal wound infection
Table 6: Variables concerning the surgical site infection
Higher SWI rates increase both postoperative morbidity and mortality,[1] and despite routine systemic antimicrobial prophylaxis in open heart surgery, deep SWI and multiresistant bacteria have become more common.[1]
Gentamicin destabilizes bacterial membranes and inhibits protein synthesis.[1] Although this drug is normally used for infections caused by gram-negative agents, it also has bactericidal effects on many grampositive agents that are directly proportional with gentamicin’s peak level. The systemic use of gentamicin has three primary disadvantages. Not only is it highly toxic, but it has many side effects. Furthermore, bacterial resistance is possible when taking low doses. However, these disadvantages become advantages when gentamicin is used topically because higher local levels of this drug can be effective against bacteria that are resistant to its minimal inhibitory concentration levels.
Besides prescribing gentamicin as a topical antibiotic for bone and soft tissue infections, recent studies have also focused on the use of local antibiotics like gentamicin in cardiac surgery,[1] with investigators usually preferring prophylactic antibiotic agents such as gentamicin-impregnated bone cement.[1] In addition, a recently published systematic review and meta-analysis of randomized trials showed a decrease in surgical site infections (SSIs) when gentamicin-collagen implants were used.[5] This study also demonstrated the possible positive effects associated with the local prophylactic use of gentamicin in surgical sites to decrease the rate of SWI. In our study, we preferred a different way of locally applying the gentamicin to the surgical site via the use of gentamicin-soaked sponges.
One of the main differences in our study was its double-blinded, placebo-controlled design. All of the previous studies that used local gentamicin-collagen implants compared these groups with a control group without an implant, which might have led to a procedural bias. In our study, the surgical team used sponges without any knowledge of whether they were soaked in gentamicin or the saline solution (placebo). The second major difference in our study was that we used a solution that contained a saline solution with or without gentamicin, which meant a reasonable reduction in cost. When we compared the cost of locally administered gentamicin with a gentamicincollagen implant, there was a nearly 30-fold difference, with the cost of our solution being $10 versus the implant cost of $300. Another difference in our study involved the time period that the gentamicin was locally applied. We used gentamicin-soaked sponges from soon after the sternotomy was performed until the sternal retractor was removed, which covered almost the whole operational process. This provided the ability to prevent microorganisms from colonizing while the operative site was open. All of the previous studies used the gentamicin-collagen implant just before the closure of the surgical site but not during the intraoperative period. Our unique study design offered another advantage in that the application area was nearly totally covered by all the incision layers on both sides. When the gentamicin-soaked sponges were inserted beneath the sternum-retractor, they covered all of the layers of skin and the sternum. Previous studies featured the use of the gentamicin-collagen implant at the posterior side of the sternum; thus, there was no contact with the anterior side of the bone, dermis, or hypodermic tissues. The most common type of SWI in cardiac surgery is type-A, which involves the skin and subcutaneous tissue. Hence, potentially, the superficial infection could then progress to deeper layers and lead to type-B SWI. Though a progression of this kind is not a guarantee, the ability of our procedure to prevent infection both superficially and at the deep surgical sides simultaneously is a major benefit.
Declaration of conflicting interests
The authors declared no conflicts of interest with
respect to the authorship and/or publication of this
article.
Funding
The authors received no financial support for the
research and/or authorship of this article.
1) Eklund AM. Prevention of sternal wound infections with
locally administered gentamicin. APMIS 2007;115:1022-4.
2) Eklund AM, Valtonen M, Werkkala KA. Prophylaxis of
sternal wound infections with gentamicin-collagen implant:
randomized controlled study in cardiac surgery. J Hosp
Infect 2005;59:108-12.
3) Sarıkaya S, Büyükbayrak F, Altaş Ö, Yerlikhan O, Fedakar
A, Rabuş M, et al. Thermoreactive nitinol clips for
re-sternotomy in cases of sternal dehiscence. Turk Gogus
Kalp Dama 2013;21:669-75.
4) Durgun M, Durgun ÖS, Özakpınar HR, Eryılmaz AT, Öktem
HF, İnözü E, et al. Approach to of infected sternotomy
wounds in the management of mediastinitis. Turk Gogus
Kalp Dama 2012;20:820-5.
5) Chang WK, Srinivasa S, MacCormick AD, Hill AG.
Gentamicin-collagen implants to reduce surgical site
infection: systematic review and meta-analysis of randomized
trials. Ann Surg 2013;258:59-65.
6) Mishra PK, Ashoub A, Salhiyyah K, Aktuerk D, Ohri S, Raja
SG, et al. Role of topical application of gentamicin containing
collagen implants in cardiac surgery. J Cardiothorac Surg
2014;9:122.
7) Sjögren J, Malmsjö M, Gustafsson R, Ingemansson R.
Poststernotomy mediastinitis: a review of conventional
surgical treatments, vacuum-assisted closure therapy and
presentation of the Lund University Hospital mediastinitis
algorithm. Eur J Cardiothorac Surg 2006;30:898-905.
8) Salehi Omran A, Karimi A, Ahmadi SH, Davoodi S,
Marzban M, Movahedi N, et al. Superficial and deep sternal
wound infection after more than 9000 coronary artery
bypass graft (CABG): incidence, risk factors and mortality.
BMC Infect Dis 2007;7:112.
9) Losanoff JE, Richman BW, Jones JW. Disruption and
infection of median sternotomy: a comprehensive review. Eur
J Cardiothorac Surg 2002;21:831-9.
10) Lu JC, Grayson AD, Jha P, Srinivasan AK, Fabri BM. Risk
factors for sternal wound infection and mid-term survival
following coronary artery bypass surgery. Eur J Cardiothorac
Surg 2003;23:943-9.
11) Leyh RG, Bartels C, Sievers HH. Adjuvant treatment of deep
sternal wound infection with collagenous gentamycin. Ann
Thorac Surg 1999;68:1648-51.
12) Vander Salm TJ, Okike ON, Pasque MK, Pezzella AT,
Lew R, Traina V, et al. Reduction of sternal infection by
application of topical vancomycin. J Thorac Cardiovasc Surg
1989;98:618-22.
13) Stemberger A, Grimm H, Bader F, Rahn HD, Ascherl R.
Local treatment of bone and soft tissue infections with the
collagen-gentamicin sponge. Eur J Surg Suppl 1997;17-26.
14) Friberg O, Svedjeholm R, Söderquist B, Granfeldt H,
Vikerfors T, Källman J. Local gentamicin reduces sternal wound infections after cardiac surgery: a randomized
controlled trial. Ann Thorac Surg 2005;79:153-61.
15) Rutten HJ, Nijhuis PH. Prevention of wound infection
in elective colorectal surgery by local application of a
gentamicin-containing collagen sponge. Eur J Surg Suppl
1997;31-5.
16) Mangram AJ, Horan TC, Pearson ML, Silver LC, Jarvis WR.
Guideline for Prevention of Surgical Site Infection, 1999.
Centers for Disease Control and Prevention (CDC) Hospital
Infection Control Practices Advisory Committee. Am J
Infect Control 1999;27:97-132.