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Hospital Bloodborne Pathogens Programs: Program Characteristics and Blood and Body Fluid Exposure Rates

Published online by Cambridge University Press:  02 January 2015

Susan E. Beekmann
Affiliation:
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa
Thomas E. Vaughn
Affiliation:
Department of Health Management and Policy, University of Iowa College of Public Health, Iowa City, Iowa
Kimberly D. McCoy
Affiliation:
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa
Kristi J. Ferguson
Affiliation:
Department of Community and Behavioral Health, University of Iowa College of Public Health, Iowa City, Iowa
James C. Torner
Affiliation:
Department of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa
Robert F. Woolson
Affiliation:
Department of Biostatistics, University of Iowa College of Public Health, Iowa City, Iowa
Bradley N. Doebbeling*
Affiliation:
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa Department of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa Iowa City Veterans Affairs Medical Center, Iowa City, Iowa
*
Department of Internal Medicine, SE 625 GH, 200 Hawkins Dr, Iowa City, IA 52242

Abstract

Objective:

To describe hospital practices and policies relating to bloodborne pathogens and current rates of occupational exposure among healthcare workers.

Participants and Methods:

Hospitals in Iowa and Virginia were surveyed in 1996 and 1997 about Standard Precautions training programs and compliance. The primary outcome measures were rates of percutaneous injuries and mucocutaneous exposures.

Results:

153 (64%) of 240 hospitals responded. New employee training was offered no more than twice per year by nearly one third. Most (79%-80%) facilities monitored compliance of nurses, housekeepers, and laboratory technicians; physicians rarely were trained or monitored. Implementation of needlestick prevention devices was the most common action taken to decrease sharps injuries. Over one half of hospitals used needleless intravenous systems; larger hospitals used these significantly more often. Protected devices for phlebotomy or intravenous placement were purchased by only one third. Most (89% of large and 80% of small) hospitals met the recommended infection control personnel-to-bed ratio of 1:250. Eleven percent did not have access to postexposure care during all working hours. Percutaneous injury surveillance relied on incident reports (99% of facilities) and employee health records (61%). The annual reported percutaneous injury incidence rate from 106 hospitals was 5.3 injuries per 100 personnel. Compared to single tertiary-referral institution rates determined more than 5 years previously, current injury rates remain elevated in community hospitals.

Conclusions:

Healthcare institutions need to commit sufficient resources to Standard Precautions training and monitoring and to infection control programs to meet the needs of all workers, including physicians. Healthcare workers clearly remain at risk for injury. Further effective interventions are needed for employee training, improving adherence, and providing needlestick prevention devices.

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

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References

1. Centers for Disease Control and Prevention. Recommendations for preventing transmission of infection with human T-lymphotropic virus type III/lymphadenopathy-associated virus in the workplace. MMWR 1985;34:681-686, 691695.Google Scholar
2. Centers for Disease Control and Prevention. Recommendations for prevention of HiV transmission in health-care settings. MMWR 1987;36(suppl 2):1S18S.Google Scholar
3. Occupational exposure to bloodborne pathogens—OSHA. Final rule. Fed Regist 1991;56:6400464182.Google Scholar
4. Garner, JS. Guideline for isolation precautions in hospitals. The Hospital Infection Control Practices Advisory Committee. Infect Control Hosp Epidemiol 1996;17:5380.CrossRefGoogle ScholarPubMed
5. Fahey, BJ, Koziol, DE, Banks, SM, Henderson, DK. Frequency of nonparenteral occupational exposures to blood and body fluids before and after universal precautions training. Am J Med 1991;90:145153.CrossRefGoogle ScholarPubMed
6. Wong, ES, Stotka, JL, Chinchilli, VM, Williams, DS, Stuart, CG, Markowitz, SM. Are universal precautions effective in reducing the number of occupational exposures among health care workers? A prospective study of physicians on a medical service. JAMA 1991;265:11231128.Google Scholar
7. Beekmann, SE, Vlahov, D, Koziol, DE, McShalley, ED, Schmitt, JM, Henderson, DK. Temporal association between implementation of universal precautions and a sustained, progressive decrease in percutaneous exposures to blood. Clin Infect Dis 1994;18:562569.CrossRefGoogle Scholar
8. Doebbeling, BN, Wenzel, RP. The direct costs of universal precautions in a teaching hospital. JAMA 1990;264:20832087.Google Scholar
9. Krasinski, K, LaCouture, R, Holzman, RS. Effect of changing needle disposal systems on needle puncture injuries. Infect Control 1987;8:5962.Google Scholar
10. Linnemann, CC Jr Cannon, C, DeRonde, M, Lanphear, B. Effect of educational programs, rigid sharps containers, and universal precautions on reported needlestick injuries in healthcare workers. Infect Control Hosp Epidemiol 1991;12:214219.CrossRefGoogle ScholarPubMed
11. Ribner, BS, Landry, MN, Gholson, GL, Linden, LA. Impact of a rigid, puncture resistant container system upon needlestick injuries. Infect Control 1987;8:6366.Google Scholar
12. Saghafi, L, Raselli, P, Francillon, C, Francioli, P. Exposure to blood during various procedures: results of two surveys before and after the implementation of universal precautions. Am J Infect Control 1992;20:5357.Google Scholar
13. Ben-David, B, Gaitini, L. The routine wearing of gloves: impact on the frequency of needlestick and percutaneous injury and on surface contamination in the operating room. Anesth Analg 1996;83:623628.CrossRefGoogle ScholarPubMed
14. Gerberding, JL, Bryant-LeBlanc, CE, Nelson, K, Moss, AR, Osmond, D, Chambers, HF, et al. Risk of transmitting the human immunodeficiency virus, cytomegalovirus, and hepatitis B virus to health care workers exposed to patients with AIDS and AIDS-related conditions. J Infect Dis 1987;156:18.CrossRefGoogle ScholarPubMed
15. Gerberding, JL, Littell, C, Tarkington, A, Brown, A, Schecter, WP. Risk of exposure of surgical personnel to patients' blood during surgery at San Francisco General Hospital. N Engl J Med 1990;322:17881793.Google Scholar
16. Kelen, GD, DiGiovanna, TA, Celentano, DD, Kalainor, D, Bisson, L, Junkins, E, et al. Adherence to Universal (barrier) Precautions during interventions on critically ill and injured emergency department patients. J Acquir Immune Defic Syndr 1990;3:987994.Google ScholarPubMed
17. Tokars, JI, Bell, DM, Culver, DH, Marcus, R, Mendelson, MH, Sloan, EP, et al. Percutaneous injuries during surgical procedures. JAMA 1992;267:28992904.Google Scholar
18. Courington, KR, Patterson, SL, Howard, RJ. Universal Precautions are not universally followed. Arch Surg 1991;126:9396.CrossRefGoogle Scholar
19. Eustis, TC, Wright, SW, Wrenn, KD, Fowlie, EJ, Slovis, CM. Compliance with recommendations for Universal Precautions among prehospital providers. Ann Emerg Med 1995;25:512515.Google Scholar
20. Friedland, LR, Joffe, M, Wiley, JF 2d Schapire, A, Moore, DF. Effect of educational program on compliance with glove use in a pediatric emergency department. Am J Dis Child 1992;146:13551358.Google Scholar
21. Gershon, RR, Vlahov, D, Felknor, SA, Vesley, D, Johnson, PC, Delclos, GL, et al. Compliance with Universal Precautions among health care workers at three regional hospitals. Am J Infect Control 1995;23:225236.Google Scholar
22. Hansen, ME, McIntire, DD, Miller, GL 3d Redman, HC. Use of Universal Precautions in interventional radiology: results of a national survey. Am J Infect Control 1994;22:15.Google Scholar
23. Henry, K, Campbell, S, Maki, M. A comparison of observed and self-reported compliance with Universal Precautions among emergency department personnel at a Minnesota public teaching hospital: implications for assessing infection control programs. Ann Emerg Med 1992;21:940946.CrossRefGoogle Scholar
24. Henry, K, Campbell, S, Collier, P, Williams, CO. Compliance with Universal Precautions and needle handling and disposal practices among emergency department staff at two community hospitals. Am J Infect Control 1994;22:129137.CrossRefGoogle ScholarPubMed
25. Hersey, JC, Martin, LS. Use of infection control guidelines by workers in healthcare facilities to prevent occupational transmission of HBV and HIV: results from a national survey. Infect Control Hosp Epidemiol 1994;15(4 Pt 1):243252.Google Scholar
26. Jeffe, DB, Mutha, S, L'Ecuyer, PB, Kim, LE, Singal, RB, Evanoff, BA, et al. Healthcare workers' attitudes and compliance with Universal Precautions: gender, occupational, and specialty differences. Infect Control Hosp Epidemiol 1997;18:710712.CrossRefGoogle ScholarPubMed
27. Lund, S, Jackson, J, Leggett, J, Hales, L, Dworkin, R, Gilbert, D. Reality of glove use and handwashing in a community hospital. Am J Infect Control 1994;22:352357.Google Scholar
28. McCarthy, GM, MacDonald, JK. The infection control practices of general dental practitioners. Infect Control Hosp Epidemiol 1997;18:699703.Google Scholar
29. McCarthy, ML, Bosse, MJ, Preas, MA, De Long, WG, Gunther, SF, Moed, BR. Orthopedic trauma surgeons' attitudes and practices towards blood-borne pathogens. J Orthop Trauma 1996;10:383388.Google Scholar
30. Michalsen, A, Delclos, GL, Felknor, SA, Davidson, AL, Johnson, PC, Vesley, D, et al. Compliance with Universal Precautions among physicians. J Occup Environ Med 1997;39:130137.Google Scholar
31. Moore, S, Goodwin, H, Grossberg, R, Toltzis, P. Compliance with universal precautions among pediatric residents. Arch Pediatr Adolesc Med 1998;152:554557.Google Scholar
32. Schillo, BA, Reischl, TM. HIV-related knowledge and precautions among Michigan nurses. Am J Public Health 1993;83:14381442.CrossRefGoogle ScholarPubMed
33. Willy, ME, Dhillon, GL, Loewen, NL, Wesley, RA, Henderson, DK. Adverse exposures and universal precautions practices among a group of highly exposed health professionals. Infect Control Hosp Epidemiol 1990;11:351356.Google Scholar
34. Scheckler, WE, Brimhall, D, Buck, AS, Farr, BM, Friedman, C, Garibaldi, RA, et al. Requirements for infrastructure and essential activities of infection control and epidemiology in hospitals: a consensus panel report. Society for Healthcare Epidemiology of America. Infect Control Hosp Epidemiol 1998;19:114124.Google Scholar
35. Eickhoff, TC, Brachman, PW, Bennett, JV, Brown, JF. Surveillance of nosocomial infections in community hospitals, I: surveillance methods, effectiveness, and initial results. J Infect Dis 1969;120:305317.Google Scholar
36. 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.Google Scholar
37. Dillman, DA. Mail and Telephone Surveys: The Total Design Method. New York, NY: John Wiley & Sons; 1978.Google Scholar
38. Campbell, MJ, Waters, WE. Does anonymity increase response rate in postal questionnaire surveys about sensitive subjects? A randomised trial. J Epidemiol Community Health 1990;44:7576.CrossRefGoogle ScholarPubMed
39. Fiset, L, Milgrom, P, Tarnai, J. Dentists' response to financial incentives in a mail survey of malpractice liability experience. J Public Health Dent 1994;54:6872.Google Scholar
40. Hoddinott, S, Bass, M. The Dillman total design survey method: a surefire way to get high survey return rates. Can Fam Physician 1986;32:23662368.Google Scholar
41. Choi, BC, Pak, AW, Purdham, JT. Effects of mailing strategies on response rate, response time, and cost in a questionnaire study among nurses. Epidemiology 1990;1:7274.Google Scholar
42. Shiono, PH, Klebanoff, MA. The effect of two mailing strategies on the response to a survey of physicians. Am J Epidemiol 1991;134:539542.Google Scholar
43. Fox, RJ, Crask, MR, Kim, J. Mail survey response rate: a meta-analysis of selected techniques for inducing response. Pub Opinion Q 1988;52:467491.Google Scholar
44. Kanuk, L, Berenson, C. Mail surveys and response rates: a literature review. Journal of Marketing Research 1975;12:440453.CrossRefGoogle Scholar
45. Maheux, B, Legault, C, Lambert, J. Increasing response rates in physicians' mail surveys: an experimental study. Am J Public Health 1989;79:638639.Google Scholar
46. American Hospital Association. American Hospital Association Guide to Healthcare Facilities, 1996. Chicago, IL: AHA 1996.Google Scholar
47. Gaynes, RP, Culver, DH, Emori, TG, Horan, TC, Banerjee, SN, Edwards, JR, et al. The National Nosocomial Infections Surveillance System: plans for the 1990s and beyond. Am J Med 1991;91(suppl 3B):116S120S.Google Scholar
48. Goldrick, BA. Infection control programs in skilled nursing long-term care facilities: an assessment, 1995. Am J Infect Control 1999;27:49.Google Scholar
49. Smith, PW, Rusnak, PG. APIC guideline for infection prevention and control in the long-term care facility. Am J Infect Control 1991;19:198215.CrossRefGoogle ScholarPubMed
50. Centers for Disease Control and Prevention. Public Health Service guidelines for the management of health-care worker exposures to HIV and recommendations for postexposure prophylaxis. MMWR 1998;47(RR-7):133.Google Scholar
51. Stotka, JL, Wong, ES, Williams, DS, Stuart, CG, Markowitz, SM. An analysis of blood and body fluid exposures sustained by house officers, medical students, and nursing personnel on acute-care general medical wards: a prospective study. Infect Control Hosp Epidemiol 1991;12:583590.Google Scholar
52. Aiken, LH, Sloane, DM, Klocinski, JL. Hospital nurses' occupational exposure to blood: prospective, retrospective, and institutional reports. Am J Public Health 1997;87:103107.Google Scholar
53. Yassi, A, McGill, ML, Khokhar, JB. Efficacy and cost-effectiveness of a needleless intravenous access system. Am J Infect Control 1995;23:5764.Google Scholar
54. Wilkinson, WE, Salazar, MK, Uhl, JE, Koepsell, TD, DeRoos, RL, Long, RJ. Occupational injuries: a study of health care workers at a northwestern health science center and teaching hospital. AAOHN J 1992;40:287293.CrossRefGoogle Scholar
55. Cardo, DM, Culver, DH, Ciesielski, CA, Srivastava, PU, Marcus, R, Abiteboul, D, et al. A case-control study of HIV seroconversion in health care workers after percutaneous exposure. Centers for Disease Control and Prevention Needlestick Surveillance Group. N Engl J Med 1997;337:14851490.Google Scholar
56. American Hospital Association. Surveillance of Nosocomial Infections. Chicago, IL: AHA; 1971.Google Scholar
57. Joint Commission on Accreditation of Hospitals. Accreditation Manual for Hospitals, 1976. Chicago, IL: JCAHO; 1976.Google Scholar
58. Haley, RW, Morgan, WM, Culver, DH, White, JW, Emori, TG, Mosser, J, et al. Update from the SENIC project. Hospital infection control: recent progress and opportunities under prospective payment. Am J Infect Control 1985;13:97108.Google Scholar
59. Jackson, MA, Williams, K, Olson-Burgess, C, Kinney, J, Olson, LC, Burry, VF. Needlestick injuries in a pediatric hospital. Pediatr Infect Dis J 1994;13:318320.Google Scholar
60. McCormick, RD, Meisch, MG, Ircink, FG, Maki, DG. Epidemiology of hospital sharps injuries: a 14-year prospective study in the pre-AIDS and AIDS eras. Am J Med 1991;91(suppl 3B):301S307S.Google Scholar
61. Pettit, LL, Gee, SQ, Begue, RE. Epidemiology of sharp object injuries in a children's hospital. Pediatr Infect Dis J 1997;16:10191023.Google Scholar
62. Khuri-Bulos, N, Toukan, A, Mahafzah, A, Al Adham, M, Faori, I, Abu Khader, I, et al. Epidemiology of needlestick and sharp injuries at a university hospital in a developing country: a 3-year study at the Jordan University Hospital, 1993 through 1995. Am J Infect Control 1997;25:322329.Google Scholar
63. McCormick, RD, Maki, DG. Epidemiology of needle-stick injuries in hospital personnel. Am J Med 1981;70:928932.Google Scholar
64. Ruben, FL, Norden, CW, Rockwell, K, Hruska, E. Epidemiology of accidental needle-puncture wounds in hospital workers. Am J Med Sci 1983;286:2630.Google Scholar
65. Whitby, M, Stead, P, Najman, JM. Needlestick injury: impact of a recapping device and an associated education program. Infect Control Hosp Epidemiol 1991;12:220225.Google Scholar
66. Eisenstein, HC, Smith, DA. Epidemiology of reported sharps injuries in a tertiary care hospital. J Hosp Infect 1992;20:271280.Google Scholar
67. Rattner, SL, Norman, SA, Berlin, JA. Percutaneous injuries on the “front line”: a survey of housestaff and nurses. Am J Prev Med 1994;10:372377.Google Scholar