ATS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Ivan W. Brown, Jr
Brian W. Hummel
William G. Marshall, Jr
John P. Collins
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Brown, I. W.
Right arrow Articles by Collins, J. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Brown, I. W., Jr
Right arrow Articles by Collins, J. P.

Ann Thorac Surg 1996;62:1783-1789
© 1996 The Society of Thoracic Surgeons


Original Articles: Cardiovascular

Toward Further Reducing Wound Infections in Cardiac Operations

Ivan W. Brown, Jr, MD, Gordon F. Moor, MD, Brian W. Hummel, MD, William G. Marshall, Jr, MD, John P. Collins, MD

Department of Cardiovascular Surgery, Watson Clinic, Lakeland, Florida

Accepted for publication June 25, 1996.


    Abstract
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Background. Serious wound infections such as mediastinitis still occur at a rate of 0.8% to 2.0%, according to the most recently published cardiac operative series.

Methods. Data from careful surveillance for infection have been collected prospectively during a 4.5-year period on 1,717 patients who underwent cardiac operations performed under direct ultraviolet C radiation.

Results. The rate for mediastinitis was 0.23%, and for deep incisional infection without mediastinitis, 0.12%; these rates are significantly lower than those for eight of nine of the most recently published cardiac series. When our infection rates were stratified using the National Nosocomial Infection Surveillance risk index, they were also significantly lower in the most important risk categories than the corresponding stratified rates collected from the participating hospitals of the Centers for Disease Control and Prevention National Nosocomial Infection Surveillance system.

Conclusions. Though we lack the proof that only a large, randomized study might provide, certainly, one possible explanation for our lower wound infection rate was the use of bactericidal ultraviolet C radiation during operation. This is a simple and effective means of minimizing operating room airborne bacteria as one possible source of these infections.


    Introduction
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Serious wound infections such as mediastinitis remain among the most dreaded complications of cardiac operations. Despite improved methods of treatment, these infections still contribute substantially to early postoperative mortality and morbidity and greatly increase hospital costs. Equally disturbing is a recent report [1] by a university center that even if patients recover from mediastinitis, it has a significant negative influence on long-term survival.

Two reports [2, 3] of small series of cardiac operations suggested a preventive effect of "high-efficiency particulate air" filtration during operation. A series of 878 cardiac operations in which a special attempt was made to eliminate operating room airborne bacteria as a possible source of operative wound infection was reported by one of us (I.W.B.) in 1968 with a 0.00% incidence of mediastinitis [4].

The purpose of this study was to determine the operative wound infection rates occurring in a series of 1,717 cardiac operations performed under direct ultraviolet C radiation. We compared these rates with other recently published cardiac operative series, particularly those collected nationwide by the Centers for Disease Control and Prevention (CDC) from the hospitals participating in the CDC National Nosocomial Infection Surveillance (NNIS) system.


    Material and Methods
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Background
All operations in this study were performed at Lakeland Regional Medical Center, a 900-bed general hospital used by the Watson Clinic, a large private clinic of 180 board-certified physicians and surgeons.

The hospital has maintained continuous detailed surveillance of nosocomial infections, carefully following the recommendations and guidelines of the CDC and, more recently, the NNIS of the CDC. The hospital Infection Control Office is staffed by a chief nurse trained in epidemiology, two assistant nurse epidemiologists, and a secretary. The office is under the direction of the Chairman of the Infections Committee with an MD infectious disease specialist as consultant.

Infection Surveillance and Data Collection
Each nurse epidemiologist makes daily rounds on assigned wards to check for any suspected or confirmed infections. The hospital bacteriology laboratory automatically forwards a copy of each positive culture report to the Infection Control Office as a further alert for follow-up by a nurse epidemiologist. If an infection is suspected, an "Infection Surveillance Record" is begun on that patient. Daily chart and patient follow-ups are started. Daily notes are made on the surveillance record summarizing any changes in the patient's temperature or condition and pertinent laboratory reports, such as white blood cell count and cultures. If an operative wound is involved, the appearance of the wound and character and amount of any drainage are noted. Antibiotics or other methods of treatment are recorded. Although the nurse epidemiologist confers with the patient's surgeon, particularly regarding the plan of treatment, it is the nurse's wound classification and estimate of severity, not the surgeon's, that is accepted. The patient's course is monitored throughout the remainder of the hospital stay, and arrangements are made for follow-up reports from his or her doctor's office after discharge.

We have used these prospective data from 1,774 cardiac operations performed under direct ultraviolet radiation by three Watson Clinic cardiac surgeons between January 1, 1988, and July 1, 1992. Unfortunately, because of limited storage space, the daily records of the nurse epidemiologists before January 1988 had been discarded. Wishing to base this study only on prospective infection data obtained by independent observers-the nurse epidemiologists-we therefore chose January 1, 1988, as the study starting date.

Fifty-seven patients who died less than 5 days postoperatively and who showed no sign of wound infection were eliminated from the study. All other patients who survived at least 5 days postoperatively were included. Thus, this study concerns 1,717 sternum-splitting cardiac operations performed on 1,623 patients, of whom 1,132 (69.83%) were male and 491 (30.17%) were female. The median age was 68 ± 9.95 years (median ± standard deviation). One hundred eleven patients (6.84%) were 80 years of age or older. The various cardiac operative procedures represented in the study are listed in Table 1Go.


View this table:
[in this window]
[in a new window]
 
Table 1. . Cardiac Operations Performed
 
The hospital charts of all the patients in the study were also reviewed for certain demographic and medical data. In addition, the outpatient records of the Watson Clinic have been reviewed on all these patients for wound infections of delayed onset for a follow-up of at least 60 days from the date of operation. Patients who had prosthetic devices implanted, such as prosthetic valves or defibrillators, had follow-up of at least 1 year for late onset of infection.

Data from all these sources were combined in a computer database using the Summit Medical Systems version 5 software (Minneapolis, MN).

Preoperative and Postoperative Procedures
Except for emergencies and those totally confined to bed, all patients had showers the evening before operation, usually with antiseptic soap. Shaving was done on the morning of operation on the patient's ward. Patients were given a loading dose of prophylactic antibiotic just before operation, with 1,708 receiving cefazolin and 1 patient receiving cephapirin. Of those sensitive to these two antibiotics, 3 received vancomycin and 5 received tobramycin.

Before moving into the operating room, the patient's eyes were covered to protect them from the ultraviolet light. Skin sterilization was either by Betadine Scrub (Purdue Frederick, Norwalk, CT) followed by painting with Betadine solution, or cleansing with 70% alcohol followed by painting with 70% alcoholic tincture of Zephiran (Winthrop Laboratories, New York, NY). After sterile drapes were applied, disposable adhesive Vidrapes or Ioban (3M Corp, St. Paul, MN) were used to cover all operative fields.

Instruments used in harvesting saphenous veins were kept separate and were removed for resterilization when this portion of the procedure was completed. Gloves also were changed. Before closing the chest wound, we occasionally irrigated the mediastinum with saline, but irrigation with an antibiotic solution was rarely used.

Unless the patient was febrile or showed signs of infection, prophylactic antibiotics were usually discontinued 48 hours postoperatively. All catheters, drains, and vascular access lines were removed as soon as possible. Unless significant drainage continued, mediastinal tubes were removed within 24 hours after operation.

Ultraviolet Bactericidal Radiation
The ultraviolet C light (253.7 nm) from ceiling-mounted ultraviolet lamps was maintained at an intensity of 20 to 25 mW•cm-2•s-1, measured at a level 30 inches above the operating room floor. The intensity was checked monthly with a calibrated ultraviolet photometer and was regulated by a tamper-proof rheostat. The ultraviolet lights remained on continuously from the night before operation until the patient was ready to leave the room after operation.

Definitions and Classification of Operative Wound Infections
We have adopted the recommendations in the consensus paper [5] of the Society for Hospital Epidemiology of America, the Association for Practitioners in Infection Control, Inc, the CDC, and the Surgical Infections Society on the surveillance of operative wound infections. They recommend the following:

  1. The CDC definitions and classification of operative wound infections [6] should be adopted by all United States hospitals without modification, and "surgical site" should be substituted for "surgical wound."
  2. Because of the marked effect that independent risk factors for surgical site infection (SSI) have on the likelihood of infection, infection rates must be stratified by risk-factor variables for purposes of meaningful comparison. To do this, they recommend the NNIS-derived risk index (see legend to Table 6Go).


View this table:
[in this window]
[in a new window]
 
Table 6. . Stratification by the National Nosocomial Infection Surveillance Risk Indexa
 
The CDC SSI classification recommended previously consists of superficial incisional SSI, deep incisional SSI, and organ/space SSI (mediastinitis). Detailed criteria defining each of these SSIs have been published [6].

Statistical Methods
Pearson's {chi}2 test was used to compare our infection rates with those of previously published cardiac operative series. In comparing our infection rates with those collected by the NNIS system, the rates were first stratified according to the NNIS risk index (see legend to Table 6Go). Statistical significance (p < 0.05) was determined by the z test, as recommended by the CDC NNIS. Risk-factor variables were first assessed individually by univariate logistic regression analysis. Those variables with p values less than 0.1 were further assessed by multivariate logistic regression at a significance level of p less than 0.05. Statistical analyses were carried out using the SPSS 6.1 Base System and Advanced Statistics software (SPSS Inc, Chicago, IL).


    Results
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Clinical details of the serious wound infections are given in Table 2Go. There were four (0.23%) organ/space SSIs, all mediastinitis, that occurred in patients undergoing coronary artery bypass grafting (CABG). Two patients (0.12%) having CABG experienced deep incisional SSIs of their chest incisions without mediastinitis. In addition, there were 19 (1.11%) superficial incisional SSIs among the CABG patients. Five (0.29%) were of the chest incisions and 14 (0.82%) occurred at saphenous vein harvest sites in the lower legs.


View this table:
[in this window]
[in a new window]
 
Table 2. . Clinical Features of Patients With Serious Operative Site Infections
 
There were no SSIs after the 251 non-CABG cardiac operations. However, primary septicemia developed in 2 diabetic women with mitral valve replacement who required prolonged ventilatory support. In 1 of these, it was a nearly terminal event. One CABG patient with mediastinitis had a secondary septicemia. One diabetic, obese woman returned 60 days after CABG because of fever and was found to have a small splenic abscess due to Peptococcus. It is presumed that this resulted from a primary bacteremia at some time postoperatively. Recovery was prompt after percutaneous drainage.

Table 3Go lists 15 risk factors for cardiac operative wound infection and their presence or absence in relation to mediastinitis plus deep chest incisional SSI and superficial incisional SSI. Among these, it is of interest that no infection developed in the 61 patients who required reoperation for continued postoperative mediastinal bleeding or in the 11 who underwent reoperation for early noninfected sternal dehiscence. Reoperation for bleeding has been found to be a strong predictor of sternal wound infection in some reported series.


View this table:
[in this window]
[in a new window]
 
Table 3. . Presence of Risk Variables
 
Risk-factor variables associated with mediastinitis and deep incisional SSI that were retained after individual univariate regression analysis (p < 0.1) for the final logistic regression model were duration of operation, chronic obstructive pulmonary disease and emergency procedure. Multivariate logistic regression analysis revealed that duration of operation was the most powerful predictor of these serious wound infections (Table 4Go). Univariate analysis of risk factors associated with superficial incisional SSI retained diabetes, duration of operation, and chronic obstructive pulmonary disease as possible predictive factors. After multivariate analysis, only diabetes and duration of operation were significant predictors of superficial incisional SSI (see Table 4Go).


View this table:
[in this window]
[in a new window]
 
Table 4. . Final Multivariate Models
 
We compared our infection rate for mediastinitis with the larger series of cardiac operations reported in the last 5 years [1, 714] (Table 5Go). Our rate of 0.23% is significantly lower by Pearson's {chi}2 test than the rates of mediastinitis in these nine collected series, with the single exception of the low rate of Nishida and associates [7], which they attributed to discriminate use of electrocautery. However, comparison of crude infection rates among institutions has limited applicability. For more meaningful and valid comparison of SSI rates, they must first be stratified as to risk variables [15].


View this table:
[in this window]
[in a new window]
 
Table 5. . Recently Published Series of Cardiac Operationsa
 
We compared our overall infection rates for CABG and non-CABG cardiac operations, stratified according to the NNIS Risk Index (Table 6Go), with corresponding stratified rate data collected by the CDC NNIS from their nationwide participating hospitals [16]. Our overall SSI rates for both CABG and non-CABG cardiac operations were significantly lower by z test (p = 0.0002 and p = 0.0096, respectively) than those of the NNIS for risk-index categories 1 (CABG) and 0 to 1 (non-CABG). Risk-index category 1 and combined risk-index categories 0 to 1 are the most important for comparison of infection rates, as 96% of our CABG operations and 79% of the collected NNIS CABG operations are in risk-index category 1, and 95% of our non-CABG cardiac operations and 81% of the NNIS non-CABG cardiac operations are in the combined risk-index categories 0 to 1. Valid rate comparisons cannot be made within categories 2 to 3 because of the small denominator in this combined category for Watson Clinic patients.


    Comment
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
The various sources suggested for the organisms causing wound infections in these clean operations remain highly speculative and controversial. No doubt some infections result from blood-borne organisms from other remote foci, including pneumonitis, infected urinary tracts, and various indwelling vascular cannulas. Perhaps a few arise from bacterial contamination of wounds during postoperative care, but it is highly probable that a great many, if not most, of these serious wound infections originate in the operating room before the wound is closed.

From the time of Lister, airborne bacteria in the operating room have been suspected as one of the sources of operative wound infections. Until recently, however, documentation of infection by this route has been lacking, perhaps accounting for the reluctance of many surgeons to give airborne infection more than passing consideration. In 1963, Walter and associates [17] at Peter Bent Brigham Hospital in Boston documented operative wound infections due to airborne Staphylococcus aureus. More recently, outbreaks of wound infections proved to be due to airborne type A streptococci have been reported [18].

These wound infections from airborne bacteria occurred despite modern air-conditioned operating rooms with air filters, positive room air pressure, and multiple room air changes per hour. As shown first by Hart [19], the air entering the operating room is virtually free of pathogenic bacteria but becomes contaminated by the personnel within it. The amount of air contamination will vary depending on the number of operating room personnel, the presence of disseminating carriers, and the duration of the operation.

Airborne bacteria have a special importance in cardiac operations because environmental air mixes with blood being aspirated through suction and returned to the patient. Blakemore and co-workers [20] took cultures during cardiac operations in the vicinity of the operative chest wounds and from the extracorporeal circuit before and after perfusion. They reported that airborne bacteria aspirated through the coronary suckers contaminated the blood of 75% of the extracorporeal circuits cultured.

In 1969, Charnley and Eftekhar [21] gave new emphasis to the importance of airborne bacteria in the operating room when their introduction of hip replacement was accompanied by a highly discouraging deep wound infection rate of 8.9%. A thorough search as to the source of these infections convinced Charnley and Eftekhar [21] that a substantial number were caused by bacteria sedimenting from the operating room air. To overcome this, Charnley and Eftekhar [21] used laminar airflow enclosure systems along with impervious gowns and closed helmets for the operative team to exclude expired air completely. This method plus high-efficiency particulate air filtration to reduce operating room airborne bacteria have been adopted by orthopedic surgeons throughout the world doing joint replacement. Unfortunately, high-efficiency particulate air filtration with laminar airflow systems is expensive to install and maintain.

Ultraviolet Bactericidal Irradiation
Direct ultraviolet radiation, as used continuously since 1936 by the orthopedic and neurosurgical services at Duke University Hospital, is another means of rapidly and markedly reducing airborne bacteria [4]. This method is simple and inexpensive, requires little maintenance, and, in fact, has been shown to be more effective in reducing airborne bacteria than laminar airflow high-efficiency particulate air filtration systems [22]. Because of the current warnings regarding the dangers of ultraviolet rays in sunlight and the poor general understanding of the biologic effects of various ultraviolet wavelengths, some facts regarding ultraviolet C radiation are briefly reviewed.

Ultraviolet C radiation used in the operating room has the shortest wavelength of ultraviolet light (100 to 260 nm) and, unlike the harmful ultraviolet A and B radiation of longer wavelengths, has the least penetration. In fact, very little, if any, ultraviolet C from sunlight reaches the earth because it is absorbed in the upper atmosphere. However, it can penetrate to and denude the outermost cell layer of the cornea, resulting in a temporary but uncomfortable superficial keratitis unless an eyeshade and glasses are worn. Ultraviolet C has no permanent effect on the eye [22]. Because it cannot penetrate to the lens of the eye, it cannot cause cataracts.

Ultraviolet C can also penetrate the epidermis of the skin which, with prolonged exposure, can cause a mild erythema if the skin is uncovered or unprotected by sunscreens. There is no evidence that this poorly penetrating wavelength of ultraviolet light can cause skin malignancies. Experimentally, this wavelength (253.7 nm) failed to produce skin malignancies in hairless mice [22]. At Duke University Hospital, where ultraviolet C has been used in the operating rooms for 60 years, there have been no ultraviolet light-induced malignancies in personnel-surgeons, nurses, or assistants [23].

The ultraviolet intensity of 20 to 25 mW•cm-2•s-1 measured at 30 inches above the operating room floor is sufficient to kill almost all bacteria in the air in seconds [22]. With constant exposure at this intensity, it will also sterilize exposed metal countertops and dry smooth surfaces. Because of its poor penetration and absorption by the thinnest layer of fluid, ultraviolet C will not harm the tissues exposed in an operative wound [22]. It does require a certain amount of eye and skin protection, but this is minimal and not uncomfortable. For details concerning ultraviolet radiation in the operating room, the reader is referred to the excellent monograph by Berg-Perier [22].

Conclusion
A serious SSI such as mediastinitis, though infrequent, can be a devastating, costly, and life-shortening complication of cardiac operations. In 1,717 cardiac operations performed during a 4.5-year period under bactericidal ultraviolet radiation, the rate of mediastinitis was significantly lower than the rates in eight of nine series of cardiac operations published in the last 5 years.

More important and meaningful, when our cardiac operations were stratified for risk variables by the CDC NNIS risk index, the overall infection rates were significantly lower in the most important risk categories than the corresponding stratified rates collected nationally by the CDC NNIS system. As noted by others [1, 7, 10], duration of operation was found to be the strongest predictor of serious chest SSI. This is not in disagreement with the hypothesis that some SSIs result from airborne bacteria.

Ultraviolet radiation has been used in the cardiac operating rooms at Lakeland Regional Medical Center from the beginning of our heart surgery program in 1972. Consequently, for comparison, we have no historic data of our own without ultraviolet radiation that might support our hypothesis that ultraviolet C radiation in the operating room helps reduce SSI.

Though we lack the proof that only a very large randomized study might provide, certainly, one possible explanation for our lower wound infection rate was the use of bactericidal ultraviolet radiation during operations. This is a simple and effective means of minimizing operating room airborne bacteria as a possible source of these infections. We recommend its further evaluation by other cardiac surgery centers.


    Acknowledgments
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
This work was supported by a grant from the Watson Clinic Foundation. Statistical analysis was provided by Dr Barbara Seeger, statistician. We are grateful for the help of Mrs Paula Owens of the Watson Clinic research department and Miss Jeanne Teaff of the secretarial services department.


    Footnotes
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Address reprint requests to Dr Brown, Watson Clinic, 1600 Lakeland Hills Blvd, Lakeland, FL 33804-5000.


    References
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 

  1. Milano CA, Kesler K, Archibald N, Sexton DJ, Jones RH. Mediastinitis after coronary bypass surgery: risk factors and long-term survival. Circulation 1995;92:2245–51.
  2. Clark RE, Amos WC, Higgins V, Bomberg KE, Weldon CS. Infection control in cardiac surgery. Surgery 1976;79:89–96.[Medline]
  3. Soots G, Leclerc H, Pol A, Savage C, Fieve R. Airborne contamination hazard in open heart surgery: efficiency of HEPA air filtration and laminar flow. J Cardiovasc Surg 1982;23:155–62.[Medline]
  4. Hart D, Postlethwait RW, Brown IW Jr, Smith WW, Johnson PA. Postoperative wound infections: a further report on ultraviolet radiation with comments on the recent (1964) National Research Council study report. Ann Surg 1968;167:728–43.[Medline]
  5. Sherertz RJ, Garibaldi RA, Marosok RD, et al. Consensus paper on the surveillance of surgical wound infections. Am J Infect Control 1992;20:263–70.
  6. Horan TC, Gaynes RP, Martone WJ, Jarvis WR, Emori TG. CDC definitions of nosocomial surgical site infections 1992: a modification of CDC definitions of surgical wound infections. Infect Control Hosp Epidemiol 1992;13:606–8.[Medline]
  7. Nishida H, Grooters RK, Soltanzadek H, Thieman KC, Schneider RF, Kim WP. Discriminate use of electrocautery on the medial sternotomy incision. J Thorac Cardiovasc Surg 1991;101:488–94.[Abstract]
  8. Hammermeister KE, Burchfiel C, Johnson R, Grover FL. Identification of patients at greatest risk for developing major complications at cardiac surgery. Circulation 1990;82(Suppl 4):380–9.
  9. Demmy TL, Park SB, Liebler GA, et al. Recent experience with major sternal wound complications. Ann Thorac Surg 1990;49:458–62.[Abstract]
  10. Loop FG, Lytle BW, Cosgrove DM, et al. Sternal wound complications after isolated coronary bypass grafting: early and late mortality, morbidity and cost of care. Ann Thorac Surg 1990;49:179–87.[Abstract]
  11. Gaynes R, Marosok R, Mowry-Hanley J, et al. Mediastinitis following coronary artery bypass surgery: a 3 year review. J Infect Dis 1991;163:117–21.[Medline]
  12. Grossi EA, Esposito R, Harris LJ, et al. Sternal wound infections and use of internal mammary artery grafts. J Thorac Cardiovasc Surg 1991;102:342–7.[Abstract]
  13. Smith MJ, Glaser RS, Osborne BJ, Buckley DC, Rath R, Schreiber JT. Sternal wound complications after open heart surgery: results from 3524 consecutive operative procedures. Contemp Surg 1993;43:197–202.
  14. Slaughter MS, Olson MM, Lee JT, Ward HB. A fifteen-year wound surveillance study after coronary artery bypass. Ann Thorac Surg 1993;56:1063–8.[Abstract]
  15. Culver DH, Horan TC, Gaynes RP, et al. Surgical wound infection rates by wound class, operative procedure and patient risk index. Am J Med 1991;91(Suppl 3B):152S–7S.[Medline]
  16. Hospital Infections Program. National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Service, United States Department of Health and Human Services, Atlanta, GA. Semi-annual report May 1995. Am J Infect Control 1995;23:377–85.[Medline]
  17. Walter CW, Knudsin RB, Brubaker MM. The incidence of airborne wound infection during operation. JAMA 1963;186:122–7.
  18. Gryska PF, O'Dea EA. Postoperative streptococcal wound infection-the anatomy of an epidemic. JAMA 1970;213:1189–92.[Abstract/Free Full Text]
  19. Hart D. Pathogenic bacteria in the air of the operating rooms. Arch Surg 1938;37:521–30.[Abstract/Free Full Text]
  20. Blakemore WS, McGarrity GJ, Thurer RJ, Wallace HW, MacVaugh H, Coriell LL. Infection by airborne bacteria with cardiopulmonary bypass. Surgery 1971;70:830–8.[Medline]
  21. Charnley J, Eftekhar N. Postoperative infection in total prosthetic replacement arthroplasty of the hip joint. Br J Surg 1969;56:641–9.[Medline]
  22. Berg-Perier M. Ultraviolet light in operating rooms. Goteborg: Kompendietryckeriet-Kallered, 1992:1–92.
  23. Enghauser M, McAney J. Exposure to germicidal ultraviolet radiation at Duke University Medical Center north. ENVR report 342. Chapel Hill, NC: University of North Carolina School of Public Health, 1993:1–17.



This article has been cited by other articles:


Home page
ChestHome page
S. Dial, D. Nguyen, and D. Menzies
Autotransfusion of Shed Mediastinal Blood: A Risk Factor for Mediastinitis After Cardiac Surgery? Results of a Cluster Investigation
Chest, November 1, 2003; 124(5): 1847 - 1851.
[Abstract] [Full Text] [PDF]


Home page
Eur. J. Cardiothorac. Surg.Home page
D. Jonkers, T. Elenbaas, P. Terporten, F. Nieman, and E. Stobberingh
Prevalence of 90-days postoperative wound infections after cardiac surgery
Eur. J. Cardiothorac. Surg., January 1, 2003; 23(1): 97 - 102.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Ivan W. Brown, Jr
Brian W. Hummel
William G. Marshall, Jr
John P. Collins
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Brown, I. W.
Right arrow Articles by Collins, J. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Brown, I. W., Jr
Right arrow Articles by Collins, J. P.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS