Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-19T03:50:35.741Z Has data issue: false hasContentIssue false

Incidence and Predictors of Surgical-Site Infections in Vietnam

Published online by Cambridge University Press:  02 January 2015

Dao Nguyen
Affiliation:
Department of Medicine, New England Medical Center-Tufts University School of Medicine, Medford, Massachusetts
William Bruce MacLeod
Affiliation:
Department of International Health, Applied Research on Child Health Project, Center for International Health, Boston University School of Public Health, Boston, Massachusetts
Dae Cam Phung
Affiliation:
National Institute of Hygiene and Epidemiology, Friendship Huu Nghi Hospital
Quyet Thang Cong
Affiliation:
Department of Anaesthesia, Friendship Huu Nghi Hospital
Viet Hung Nguyen
Affiliation:
Division of Infection Control, Bach Mai Hospital, Hanoi, Vietnam
Van Hoa Nguyen
Affiliation:
Department of Clinical Microbiology, Friendship Huu Nghi Hospital
Davidson Howes Hamer*
Affiliation:
Department of Medicine, New England Medical Center-Tufts University School of Medicine, Medford, Massachusetts Department of International Health, Applied Research on Child Health Project, Center for International Health, Boston University School of Public Health, Boston, Massachusetts
*
Boston University School of Public Health, 715 Albany St, T4w, Boston, MA 02118

Abstract

Objective:

To determine the incidence of, and risk factors for, surgical-site infections (SSIs).

Design:

Prospective observational study of all patients undergoing surgery during a 3-month period.

Setting:

Two urban hospitals in Hanoi, Vietnam.

Patients:

All 697 patients admitted for emergent and elective surgery.

Methods:

Data were collected on all patients undergoing surgery during a 3-month period at each hospital. We stratified the data by type of surgery, wound class, and Study on the Efficacy of Nosocomial Infection Control (SENIC) risk index. The analysis was done with the data sets from each hospital separately and with the combined data. The risk factors for SSI were identified using a logistic-regression model.

Results:

During the period of observation, 10.9% of 697 patients had SSI. The SSI rate was 8.3% for clean wounds, 8.6% for clean-contaminated, 12.2% for contaminated, and 43.9% for dirty wounds. The lowest rate of SSI (2.4%) was found in obstetric-gynecologic procedures and the highest rate (33.3%) in cardiothoracic operations. Using the SENIC risk index, the incidence of SSI in low-risk patients was 5.1%; for medium-risk patients, 13.5%, and high-risk patients, 24.2%. In a logistic-regression model, abdominal surgery (odds ratio [OR], 4.46; P<.01) and wound class IV (OR, 5.67; P<.01) were significant predictors of SSI. All patients were treated with prolonged courses of perioperative antibiotics. Overall infection control practices were poor as a result of deficient facilities, limited surgical instruments, and a lack of proper supplies for wound care and personal hygiene.

Conclusions:

There was a higher incidence of SSI in low-risk patients in Vietnam compared with developed countries. Excessive reliance on antimicrobial therapy as a means to limit SSI places patients at higher risk of adverse effects from treatment and also may contribute to worsening problems with antimicrobial resistance. Establishment of an infection control program with guidelines for antimicrobial use should improve the use of prophylactic antibiotics and attention to proper surgical and wound-care techniques. These interventions also should reduce the incidence of SSI and its associated morbidity and costs.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2001

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Horan, TC, Culver, DH, Gaynes, RP, Jarvis, WR, Edwards, JR, Reid, CR. Nosocomial infections in surgical patients in the United States, January 1986-June 1992. Infect Control Hasp Epidemiol 1993;14:7380.CrossRefGoogle ScholarPubMed
2. Huskins, WC, O'Rourke, EJ, Rhinehart, E, Goldmann, DA. Infection control in countries with limited resources. In: Mayhall, CG, ed. Hospital Epidemiology and Infection Control. 2nd ed. Philadelphia, PA: Williams & Wilkins; 1999:14891513.Google Scholar
3. Fitzroy, AO, Brooks, PJ, Richardson, EG. Nosocomial infections in a rural regional hospital in a developing country: infection rates by site, service, cost, and infection control practices. Infect Control Hosp Epidemiol 1998;19:136140.Google Scholar
4. Khuri-Bulos, NA. Nosocomial infections in the intensive care units at a university hospital in a developing country: comparison with National Nosocomial Infections Surveillance intensive care unit rates. Am J Infect Control 1999;27:547552.CrossRefGoogle Scholar
5. Ponce-de-Leon, S. The needs of developing countries and the resources required. J Hosp Infect 1991;18(suppl A):376381.CrossRefGoogle ScholarPubMed
6. Johnson & Johnson SA. Inc and the Ministry of Health of Vietnam. From the Proceedings for the Conference on Hospital Infection Control; April 1998.Google Scholar
7. Cruse, PJE, Foord, R. A five-year prospective study of 23,649 surgical wounds. Arch Surg 1973;107:206210.CrossRefGoogle Scholar
8. 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;13:606608.CrossRefGoogle ScholarPubMed
9. Pagano, M, Gauvreau, K. Principles of Biostatistics. Pacific Grove, CA: Duxbury Press; 1993.Google Scholar
10. Hosmer, DW, Lemeshow, S. Applied Logistic Regression. New York City, NY: John Wiley & Sons; 1989.Google Scholar
11. Haley, RW, Culver, DH, Morgan, WM, White, JW, Emori, TG, Hooton, TM. Identifying patients at high risk of surgical wound infection: a simple multivariate index of patient susceptibility and wound contamination. Am J Epidemiol 1985;121:206215.CrossRefGoogle ScholarPubMed
12. Culver, DH, Horan, TC, Gaynes, RP, Martone, WJ, Jarvis, WR, Emori, GE. Surgical wound infection rates by wound class, operative procedure, and patient risk index. Am J Med 1991;91(suppl 3B):S152S157.CrossRefGoogle ScholarPubMed
13. Eltahawy, AT, Mokhtar, AA, Khalaf, RM, Bahnassy, AA. Postoperative wound infection at a university hospital in Jeddah, Saudi Arabia. J Hosp Infect 1992;21:7983.CrossRefGoogle Scholar
14. Garibaldi, RA, Cushing, D, Lerer, T. Risk factors for postoperative infection. Am J Med 1991;91(3B):158S163S.CrossRefGoogle ScholarPubMed
15. Haley, RW. Nosocomial infections in surgical patients: developing valid measures of intrinsic patient risk. Am J Med 1991;91(suppl 3B):145S151S.CrossRefGoogle ScholarPubMed
16. Delgado-Rodriguez, M, Sillero-Arenas, M, Medina-Cuadros, M, Martinez-Gallero, G. Nosocomial infections in surgical patients: comparison of two measures of intrinsic patient risk. Infect Control Hosp Epidemiol 1997;18:1923.CrossRefGoogle ScholarPubMed
17. Emori, TG, Culver, DH, Horan, TC, Jarvis, WR, White, JW, Olson, DR, et al. National Nosocomial Infections Surveillance System (NNIS): description of surveillance methods. Am J Epidemiol 1991;19:1935.Google ScholarPubMed
18. Owens, WD, Felts, JA, Spitznagel, EL. ASA physical status classification: a study of the consistency of the ratings. Anesthesiology 1978;49:239243.CrossRefGoogle ScholarPubMed
19. Keats, AS. The ASA classification of physical status: a recapitulation. Anesthesiology 1978;49:239243.CrossRefGoogle ScholarPubMed
20. Cruse, P. Wound Infection surveillance. Rev Infect Dis 1981;3:734737.CrossRefGoogle ScholarPubMed
21. Mangram, AJ, Horan, TC, Pearson, ML, Silver, LC, Jarvis, WR. Guideline for prevention of surgical site infection. Infect Control Hosp Epidemiol 1999;20:247278.CrossRefGoogle ScholarPubMed
22. Sherertz, RJ, Garibaldi, RA, Marosok, RD, Mayhall, CG, Scheckler, WE, et al. Consensus paper on the surveillance of surgical wound infections. Infect Control Hosp Epidemiol 1992;20:263270.Google Scholar
23. Holzheimer, RG, Haupt, W, Thiede, A, Schwarzkopf, A. The challenge of postoperative infections: does the surgeon make a difference? Infect Control Hosp Epidemiol 1997;18:449456.CrossRefGoogle Scholar
24. Danchaivijitr, S, Jitreecheue, L, Chokloikaew, S, Suthisanon, L, Tantiwatanapaibool, Y, Poomsuwan, W. A national study on surgical wound infections 1992. J Med Assoc Thai 1995;78(suppl 2):S73S77.Google Scholar
25. Gedebou, M, Habte-Gabr, E, Kronwall, G, Yoseph, S. Hospital-acquired infections among obstetric and gynaecological patients at Tikur Anbessa Hospital, Addis Ababa. J Hosp Infect 1988;11:5059.CrossRefGoogle ScholarPubMed
26. Jepsen, OB, Jensen, LP, Zimakoff, J, Friis, H, Bissoonauthsing, CN, Kasenally, AT, et al. Prevalence of infections and use of antibiotics among hospitalized patients in Mauritius: a nationwide survey of a national infection control programme. J Hosp Infect 1993;25:271278.CrossRefGoogle ScholarPubMed
27. Mayon-White, RT, Ducel, G, Kereseselidze, T, Tikomirov, E. An international survey of the prevalence of hospital acquired infection. J Hosp Infect 1988;11(suppl A):4348.CrossRefGoogle ScholarPubMed
28. Tikomirov, E. WHO programme for the control of hospital infections. Chemioterapia 1987;6:148151.Google Scholar
29. Tran, TS, Jamulitrat, S, Chongsuvivatvong, V, Geater, A. Postoperative hospital-acquired infection in Hungvuong Obstetric and Gynaecological Hospital, Vietnam. J Hosp Infect 1998;40:141147.CrossRefGoogle ScholarPubMed
30. de Oliveira, TC, Branchini, ML. Infection control in a Brazillian regional multihospital system. Am J Infect Control 1999;27:262269.CrossRefGoogle Scholar
31. Haley, RW, Culver, DH, White, JW, Morgan, WM, Emori, TG, Munn, VP, et al. The efficacy of infection surveillance and control programs in preventing nosocomial infections in US hospitals. Am J Epidemiol 1985;121:182205.CrossRefGoogle ScholarPubMed
32. el-Nageh, MM. How to combat nosocomial infection in developing countries. World Health Forum 1995;16:262269.Google ScholarPubMed
33. Meers, PD. Infection control in developing countries. J Hosp Infect 1988;11S:406410.CrossRefGoogle Scholar
34. Classen, DC, Evans, RS, Pestotnik, SL, Horn, SD, Menlove, RL, Burke, JP. The timing of prophylactic administration of antibiotics and the risk of surgical-wound infection. N Engl J Med 1992;326:281286.CrossRefGoogle ScholarPubMed
35. Goldmann, DA. Control of nosocomial antimicrobial-resistant bacteria: a strategic priority for hospitals worldwide. Clin Infect Dis 1997;24S:139145.CrossRefGoogle Scholar
36. Hart, CA. Antimicrobial resistance in developing countries. BMJ 1998;317:647650.CrossRefGoogle ScholarPubMed
37. Lim, VK, Cheong, YM, Suleiman, AB. The use of surgical antibiotic prophylaxis in seven Malaysian hospitals. Southeast Asian J Trop Med Public Health 1994;25:698701.Google ScholarPubMed
38. Okeke, IN. Socioeconomic and behavioral factors leading to acquired bacterial resistance to antibiotics in developing countries. Emerg Infect Dis 1999;5:1827.CrossRefGoogle ScholarPubMed
39. Ministry of Health of Vietnam. Minimum Health Data Set (1993-1996). Hanoi, Vietnam: Health Statistics and Informatic Division, Ministry of Health of Vietnam.Google Scholar
40. Classen, DC, Evans, RS, Pestotnik, SL, Horn, SD, Menlove, RL, Burke, JE. The timing of prophylactic administration of antibiotics and the risk of surgical-wound infection. N Engl J Med 1992;326:281286.CrossRefGoogle ScholarPubMed
41. Reggiori, A, Ravera, M, Cocozza, E, Andreata, M, Mukasa, F. Randomized study of antibiotic prophylaxis for general and gynaecological surgery from a single centre in rural Africa. Br J Surg 1996;83:356359.CrossRefGoogle ScholarPubMed
42. Thanlikikul, V. Impact of an educational program on antibiotic use in a tertiary care hospital in a developing country. J Clin Epidemiol 1998;51:773778.CrossRefGoogle Scholar