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The Journal of Tehran University Heart Center logoLink to The Journal of Tehran University Heart Center
. 2014 Jul 3;9(3):120–123.

Comparison of the Effectiveness of Continuous versus Intermittent Cefazolin for the Prevention of Infection after Off-Pump Coronary Artery Bypass Graft

Seyed Khalil Forouzannia 1, Ali Akbar Karimi-Bondarabadi 1,2,*, Mostafa Bagherinasab 1, Mohammadtaghi Sarebanhassanabadi 1
PMCID: PMC4393834  PMID: 25870629

Abstract

Background:

Surgical site infection is known as a common complication after cardiac surgery, and Cefazolin is the best prophylactic antibiotic to prevent this complication. The goal of this study was to evaluate the effect of continuous and intermittent Cefazolin for the prevention of superficial surgical site infection following off-pump coronary artery bypass (OPCAB).

Methods:

This prospective randomized clinical trial study was conducted on 141 patients candidated for OPCAB and divided into two groups. This study was performed between February 2011 and February 2012 in the Iranian city of Yazd. Patients in both groups received 2 g of Cefazolin as a starting dose and at 30 minutes before incision. Definition of surgical site infections was according to the Centers for Disease Control and Prevention Criteria (CDC-criteria). In the continuous infusion group (n = 74), 3 g of Cefazolin was infused over a 24-hour period after surgery. In the intermittent group (n = 67), 1 g of Cefazolin was administered at 3, 11, and 19 hours after the starting dose. Hyperlipidemia, diabetes, hypertension, smoking, history of heart disease, and incidences of superficial infection were compared between the two groups. Duration of follow- up was 4 weeks.

Results:

The mean age of the patients was 60.49 ± 10.63 years. The patients were 30.5% female and 69.5% male. There were no significant differences in age, body surface area, duration of operation, number of distal grafts, number of proximal grafts, and duration of hospital stay before heart surgery between two groups. The incidence of infection in intermittent group was (7.5%) and in continuous groups was (2.7%). There was no significant difference in the incidence of infection between the two groups (p value = 0.26).

Conclusion:

Our findings in this study showed no significant differences between continuous and intermittent Cefazolin for the prevention of superficial surgical site infections after OPCAB.

Keywords: Cefazolin; Infection; Coronary artery bypass, off -pump

Introduction

Cardiac surgery is known as an invasive and complex operation. Patients candidated for off-pump coronary artery bypass (OPCAB) are at risk of surgical site infection.1 Infection after cardiac surgery is mostly related to sternotomy and vein graft harvesting site incisions.2 Reported incidence rate of postoperative infection in cardiac surgery varies from 7% to 18%, and deep sternal wound infection has a reported incidence rate of 1% to 3%.3 These complications can cause mortality rates of up to 30%. Prophylactic antibiotics are recommended in cardiac surgery because of high mortality in patients with infections. The benefit of prophylactic antibiotics in cardiovascular surgery has been shown in some studies.45 Staphylococci are the most common organisms that exist in the vein harvesting site and chest wound infections.6 Cefazolin is the mainstay of prophylaxis in cardiac surgery thanks to its low toxicity and extensive microbial coverage.7 Today in cardiac surgery, Cefazolin is administered intermittently as an intravenous bolus with a dose of 1 - 2 g before anesthesia induction and repeated after the onset of cardiopulmonary bypass or at wound closure and then two to three doses every 8 hours.7 Cefazolin has a short elimination half time.8 Accordingly, in this study, Cefazolin was used as a continuous infusion in order to counteract this effect. It is clear that a continuous infusion of Cefazolin after a bolus dose can provide continuously higher serum levels of Cefazolin compared to a bolus injection.8 It is, therefore, expected that a continuous infusion can be more effective as a prophylactic antibiotic therapy in cardiac surgery. However, some studies have shown no differences between the continuous and intermittent methods for the prevention of superficial surgical site infection.9

The aim of the present study was to compare bolus and continuous prophylactic Cefazolin injections in OPCAB candidates.

Methods

This prospective randomized clinical trial study, performed between February 2011 and February 2012 in the Iranian city of Yazd, recruited 141 patients candidated for OPCAB. The study was approved by the Ethics Committee of the Cardiovascular Research Center of Shahid Sadoughi University of Medical Sciences. This study was approved by Iranian Registry of Clinical Trial with IRCT-code: 2014041917026N1. All patients gave informed consent to participate in this study. The study population was divided into two groups through simple randomization: continuous and intermittent groups. Both groups received the same anesthesia and perioperative management and received 2 g of Cefazolin as a starting dose 30 minutes before incision. In the continuous infusion group (n = 74), 3 g of Cefazolin was continuously infused over a 24-hour period. In the intermittent group (n = 67), 1 g of Cefazolin was administered at 3, 11, and 19 hours after the starting dose. Definition of surgical site infections was according to the Centers for Disease Control and Prevention criteria (CDC-criteria). In this study, the evaluation of infections was based on the superficial type of the surgical site infection. Patients with a history of antibiotic therapy during the 72-hour period before surgery, severe renal and liver failure, and pregnancy were excluded from the study. Duration of follow-up was 4 weeks. Data were analyzed using the chi-squared and t-tests.

Results

This prospective randomized clinical trial was conducted on 141 patients at a mean age of 60.49 ± 10.63 years. Demographic data are presented in Table 1. Hyperlipidemia, diabetes mellitus, hypertension, smoking, and history of heart disease had no statically significant differences between the two groups (Table 1).

Table 1.

Characteristics of the two groups*

Variable Intermittent Group (n=67) Continuous Group (n=74) Total (n=141) P value





Age (y) 62.83±13.57 58.15±12.14 60.49±14.63 0.923
Gender
  Male 41 (61.2) 57 (77.1) 98 (69.5) 0.051
  Female 26 (38.8) 17 (22.9) 43 (30.5)
Hyperlipidemia 42 (62.7) 45 (60.8) 87 (61.7) 0.819
Diabetes 40 (59.7) 41 (55.4) 81 (57.4) 0.663
Hypertension 34 (50.7) 32 (43.2) 66 (46.8) 0.373
Smoking 45 (67.2) 49 (66.2) 94 (66.7) 0.905
History of heart disease 38 (56.7) 47 (63.5) 85 (60.3) 0.410
*

Data are presented as mean±SD or n (%)

The t-test analysis revealed no significant differences in terms of age (p value = 0.9), body surface area (p value = 0.77), surgery time (p value = 0.7), number of distal grafts (p value = 0.14), number of proximal grafts (p value = 0.36), and bedding time before heart surgery (p value = 0.33) between the two groups. Also, there was no significant difference in the incidence rate of postoperative infection between the two groups (p value = 0.26) (Table 2).

Table 2.

Incidence of infection between the two groups*

Superficial infection Bolus (n=69) Continuous (n=74) Total P value





No 62 (92.5) 72 (97.3) 134 (95.0) 0.264
Yes 5 (7.5) 2 (2.7) 7 (5.0)
*

Data are presented as n (%)

Discussion

Surgical site infection is one of the most important complications after surgery and is known as a second most common cause of nosocomial infections.10 Wound infection can even lead to an increased financial burden by prolonging hospitalization.11 Risk factors that increase the incidence of postoperative wound infection include obesity, diabetes mellitus, use of internal mammary artery graft, advanced age, male gender, chronic obstructive pulmonary disease, smoking, and preoperative hospital stay of more than 5 days.12 Some studies have suggested that diabetes mellitus can contribute to a more severe surgical site infection.13 On the other hand, smoking is thought to exert no significant effect on the rate of surgical site infection.14

Overall, it is clear that an effective prophylactic antibiotic should be an appropriate antibiotic with a peak blood level before skin incision and an adequate level during surgery and the early postoperative period.15 Cefazolin has a time-dependent killing feature; this means that the maximal effect of this antibiotic requires exposure to antibiotic concentrations above the minimum inhibitory concentration (MIC) to have the maximum efficacy.

In a study conducted by Zanetti G et al.,16 the results demonstrated that intermittent Cefazolin could reduce surgical site infection by more than 16% in patients with prolonged (more than 240 minutes) surgical procedures. Waltrip T et al.17 indicated that beta-lactam antibiotics, when infused continuously, might be more effective than intermittent dosing in perioperative prophylaxis against wound infection. Kasiakou SK et al.18 reported that there was no difference in mortality and nephrotoxicity between their two study groups of continuous and intermittent intravenous administration. A systematic review, performed by Roberts et al. 19 showed that a continuous infusion of beta-lactam antibiotics had no potency to change the mortality rate statistically. In our study, the mortality rate was zero. In the Roberts et al.19 study, a continuous infusion of beta-lactam antibiotics did not influence the status of clinical cure; the authors, however, suggested that a continuous infusion had the same effect as a higher dose of a bolus administration. Zeller V et al.20 demonstrated that the administration of a continuous infusion of Cefazolin to treat bone and joint infection was practical, efficient, safe, and available. Harbath S et al.21 concluded that prolonging prophylaxis for more than 48 hours did not reduce the incidence of surgical site infection in cardiac surgery but it could increase resistance to microorganisms. Douglas A et al.22 suggested that 2 g of bolus Cefazolin 30 minutes prior to surgical incision could provide acceptable plasma and interstitial fluid concentrations for microorganisms in patients candidated for abdominal aortic aneurysm open repair surgery. Finkelstein R et al.23 indicated that Vancomycin and Cefazolin had similar effects for preventing surgical site infection in open heart surgery; nevertheless, the authors reported that the side effects of Vancomycin included hypotension and resistance to microorganisms. Consequently, in the present study, we chose to utilize Cefazolin as the best prophylactic antibiotic in cardiac surgery. In previous studies, no significant differences were found in terms of the length of hospital stay and intensive care unit stay between the continuous infusion and the bolus injection of beta-lactam antibiotics.24 In a study by Admebri et al.,9 no patient had developed surgical site infection at 30 days after surgery. Furthermore, the authors found that a continuous infusion of Cefazolin after bolus Cefazolin administration provided better Cefazolin serum levels without increased costs and higher total dose. In our study, 7 patients acquired infection; the difference between the two groups, however, did not constitute a statistical significance.

Conclusion

In light of the findings of the present study, there seem to be no significant differences between continuous and intermittent infusions of Cefazolin for the prevention of superficial surgical site infection after OPCAB. Nonetheless, further studies with more patients and longer follow-up periods are recommended.

Acknowledgments

This study was approved and supported by Shahid Sadoughi University of Medical Sciences. The authors are indebted to all the physicians, nurses, and patients who participated in this research.

References

  • 1. Fernandez-Ayala M, Nan DN, Farinas-Alvarez C, Revuelta JM, Gonzalez-Macias J, Farinas MC. Surgical site infection during hospitalization and after discharge in patients who have undergone cardiac surgery. Infect Control Hosp Epidemiol 2006; 27: 85–88. [DOI] [PubMed] [Google Scholar]
  • 2. Ridderstolpe L, Gill H, Granfeldt H, Ahlfeldt H, Rutberg H. Superficial and deep sternal wound complications: incidence, risk factors and mortality. Eur J Cardiothorac Surg 2001; 20: 1168–1175. [DOI] [PubMed] [Google Scholar]
  • 3. Austin TW, Coles JC, Burnett R, Goldbach M. Aortocoronary bypass procedures and sternotomy infections: a study of antistaphylococcal prophylaxis. Can J Surg 1980; 23: 483–485. [PubMed] [Google Scholar]
  • 4. Tamayo E, Gualis J, Flórez S, Castrodeza J, Eiros Bouza JM, Alvarez FJ. Comparative study of single-dose and 24-hour multiple-dose antibiotic prophylaxis for cardiac surgery. J Thorac Cardiovasc Surg 2008; 136: 1522–1527. [DOI] [PubMed] [Google Scholar]
  • 5. Carignan A, Allard C, Pepin J, Cossette B, Nault B, Valiquette L. Risk of clostridium difficile infection after perioperative antibacterial prophylaxis before and during an outbreak of infection due to a hypervirulent strain. Clin Infect Dis 2008; 46: 1838–1843. [DOI] [PubMed] [Google Scholar]
  • 6. Scher KS. Studies on the duration of antibiotic administration for surgical prophylaxis. Am Surg 1997; 63: 59–62. [PubMed] [Google Scholar]
  • 7. Edwards FH, Engelman RM, Houck P, Shahian DM, Bridges CR. The Society of Thoracic Surgeons Practice Guideline Series: antibiotic prophylaxis in cardiac surgery, part I: duration. Ann Thorac Surg 2006; 81: 397–404. [DOI] [PubMed] [Google Scholar]
  • 8. Moellering RC, Jr, Swartz MN. Drug therapy: the newer cephalosporins. N Engl J Med 1976; 294: 24–28. [DOI] [PubMed] [Google Scholar]
  • 9. Adembri C, Ristori R, Chelazzi C, Arrigucci S, Cassetta MI, Gaudio ARD, Novelli A. Cefazolin bolus and continuous administration for elective cardiac surgery: improved pharmacokinetic and pharmacodynamic parameters. J Thorac Cardiovasc Surg 2010; 140: 471–475. [DOI] [PubMed] [Google Scholar]
  • 10. Burke JP. Infection control - a problem for patient safety. N Engl J Med 2003; 348: 651–656. [DOI] [PubMed] [Google Scholar]
  • 11. Mohammdzade MA, Akbar MH, Mohammdzade A. Complications of elective abdominal aortic aneurysm surgery. Acta Medica Iranica 2007; 45: 116–120. [Google Scholar]
  • 12. Hollenbeak CS, Murphy DM, Koenig S, Woodward RS, Dunagan WC, Fraser VJ. The clinical and economic impact of deep chest surgical site infections following coronary artery bypass graft surgery. Chest 2000; 118: 397–402. [DOI] [PubMed] [Google Scholar]
  • 13. Borger MA, Rao V, Weisel RD, Ivanov J, Cohen G, Scully HE, David TE. Deep sternal wound infection: risk factors and outcomes. Ann Thorac Surg 1998; 65: 1050–1056. [DOI] [PubMed] [Google Scholar]
  • 14. Vuorisalo S, Haukipuro K, Pokela R, Syrjälä H. Risk features for surgical-site infections in coronary artery bypass surgery. Infect Control Hosp Epidemiol 1998; 19: 240–247. [DOI] [PubMed] [Google Scholar]
  • 15. Engelman R, Shahian D, Shemin R, Guy TS, Bratzler D, Edwards F, Jacobs M, Fernando H, Bridges C, Workforce on Evidence-Based Medicine, Society of Thoracic Surgeons The Society of Thoracic Surgeons Practice Guideline Series: antibiotic prophylaxis in cardiac surgery, part II: antibiotic choice. Ann Thorac Surg 2007; 83: 1569–1576. [DOI] [PubMed] [Google Scholar]
  • 16. Zanetti G, Giardina R, Platt R. Intraoperative redosing of cefazolin and risk for surgical site infection in cardiac surgery. Emerg Infect Dis 2001; 7: 828–831. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Waltrip T, Lewis R, Young V, Farmer M, Clayton S, Myers S, Gray LA, Jr, Galandiuk S. A pilot study to determine the feasibility of continuous cefazolin infusion. Surg Infect (Larchmt) 2002; 3: 5–9. [DOI] [PubMed] [Google Scholar]
  • 18. Kasiakou SK, Sermaides GJ, Michalopoulos A, Soteriades ES, Falagas ME. Continuous versus intermittent intravenous administration of antibiotics: a meta-analysis of randomised controlled trials. Lancet Infect Dis 2005; 5: 581–589. [DOI] [PubMed] [Google Scholar]
  • 19. Roberts JA, Webb S, Paterson D, Ho KM, Lipman J. A systematic review on clinical benefits of continuous administration of beta-lactam antibiotics. Crit Care Med 2009; 37: 2071–2078. [DOI] [PubMed] [Google Scholar]
  • 20. Zeller V, Durand F, Kitzis MD, Lhotellier L, Ziza JM, Mamoudy P, Desplaces N. Continuous cefazolin infusion to treat bone and joint infections: clinical efficacy, feasibility, safety, and serum and bone concentrations. Antimicrob Agents Chemother 2009; 53: 883–887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Harbarth S, Samore MH, Lichtenberg D, Carmeli Y. Prolonged antibiotic prophylaxis after cardiovascular surgery and its effect on surgical site infections and antimicrobial resistance. Circulation 2000; 27: 2916–2921. [DOI] [PubMed] [Google Scholar]
  • 22. Douglas A, Udy AA, Wallis SC, Jarrett P, Stuart J, Lassig-Smith M, Deans R, Roberts MS, Taraporewalla K, Jenkins J, Medley G, Lipman J, Roberts JA. Plasma and tissue pharmacokinetics of cefazolin in patients undergoing elective and semielective abdominal aortic aneurysm open repair surgery. Antimicrob Agents Chemother 2011; 55: 5238–5242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Finkelstein R, Rabino G, Mashiah T, Bar-El Y, Adler Z, Kertzman V, Cohen O, Milo S. Vancomycin versus cefazolin prophylaxis for cardiac surgery in the setting of a high prevalence of methicillin-resistant staphylococcal infections. J Thorac Cardiovasc Surg 2002; 123: 326–332. [DOI] [PubMed] [Google Scholar]
  • 24. Mohd Hafiz AA, Staatz CE, Kirkpatrick CM, Lipman J, Roberts JA. Continuous infusion vs. bolus dosing: implications for beta-lactam antibiotics. Minerva Anestesiol 2012; 78: 94–104. [PubMed] [Google Scholar]

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