Volume 11, Number 4—April 2005
Patient Contact Recall after SARS Exposure
We reinterviewed healthcare workers who had been exposed to a patient with severe acute respiratory syndrome (SARS) in an intensive care unit to evaluate the effect of time on recall reliability and willingness to report contact activities and infection control precautions. Healthcare workers reliably recalled events 6 months after exposure.
Severe acute respiratory syndrome (SARS) quickly spread within hospitals after it was first identified in Toronto, Canada, in March 2003. Healthcare workers who cared for severely ill patients with SARS were at high risk of acquiring an infection (1).
Risk factors associated with SARS transmission have been assessed by using retrospective data from medical chart reviews and healthcare worker interviews (2–4). Infection control practitioners routinely use this method to determine the degree of exposure to communicable diseases in hospitals, but its reliability and validity are unknown. To better understand the impact of time on recall reliability and healthcare workers’ willingness to report infection control breaches, we reinterviewed a cohort of healthcare workers who had been exposed to a patient with SARS and who had previously been studied (3).
During the first Toronto SARS outbreak in March 2003, 69 healthcare workers at risk for SARS were interviewed a median of 1.2 months (range 1 to 1.5 months) after exposure (3). Five months (range 4.8 to 5.3 months) after participating in this initial study, 30 of these healthcare workers were asked to participate in another study. These workers were eligible for participation in this second investigation because they had entered the index patient’s room from 24 hours before intubation to 4 hours after intubation. Both investigations involved telephone or face-to-face interviews to determine the amount of time the worker had spent in contact with the patient, the activities that had occurred while the worker was in the patient’s room, and the personal protective equipment used by the worker. The second questionnaire was more detailed than the first but contained a substantial number of questions that were identical to those in the first questionnaire.
Responses to identical questions in the initial and follow-up interviews were compared and expressed as proportions. Responses obtained during the initial interview were considered the reference standard for comparison with follow-up interview responses. Agreement between the initial and follow-up responses was quantified by using the kappa statistic and confidence intervals. The kappa statistic (κ) is a commonly used measurement of agreement or repeatability in epidemiologic studies. Kappa values from 0.20 to 0.39 indicated fair agreement, values from 0.40 to 0.59 indicated moderate agreement, values from 0.60 to 0.79 indicated good agreement, and values >0.80 indicated excellent agreement (5).
Twenty-seven of the 30 eligible healthcare workers agreed to the second interview (Table 1). The proportion of healthcare workers who reported the same exposure in the follow-up interview as during the initial interview was >80% for most respiratory and airway management activities and >90% for procedures such as vascular catheter insertion. However, the proportion of similar responses was lower for routine patient care activities such as bedding change (67%) and nebulizer treatments (70%) (Table 2).
Agreement between initial and follow-up responses was high for most respiratory and airway management activities, including suctioning after intubation (κ = 0.63), manipulation of oxygen face mask or tubing (κ = 0.70), manual ventilation (κ = 0.63), and mechanical ventilation (κ = 0.70). Agreement was fair to moderate for the following respiratory procedures: intubation (κ = 0.46), suctioning before intubation (κ = 0.34), and patient coughing while the healthcare worker was in the room (κ = 0.38). Agreement was high for routine patient care activities, including emptying urinary catheter collection bag or collecting urine sample (κ = 0.63), bathing the patient (κ = 0.87), and performing oral care or obtaining nasal swabs (κ = 0.71). Agreement was also high for inserting an arterial line (κ = 0.75) and for cleaning the patient’s room (κ = 0.65).
Healthcare workers were asked during both interviews to estimate whether they had spent >10 minutes, >30 minutes, or >4 hours in the patient’s room. Twenty-two (88%) of the 25 healthcare workers that participated in both interviews provided the same estimates of exposure duration. Two healthcare workers overestimated and 1 underestimated the time spent in the patient’s room. Kappa values (κ = 0.52) did not vary according to the duration of exposure.
Relative to their initial responses, on follow-up, healthcare workers tended to overestimate their presence in the patient’s room during respiratory and airway management activities, particularly nebulization therapy. However, during the second interview, they were less likely to report being in the room while a bi-level positive air pressure unit was being used or while bedding was being changed. The rates of overestimated responses versus underestimated responses for other patient care activities were similar (Table 2). Healthcare workers who developed cases of laboratory–confirmed SARS were not more or less likely to remember their presence or absence during patient care activities (data not shown).
In the hospital, use of additional precautions (gown, gloves, and surgical masks for room entry) for methicillin-resistant Staphylococcus aureus was practiced by the healthcare workers (6). Compliance varied among healthcare workers, but the proportion of workers with the same response during the follow-up interview was >80% for all infection control precautions, except wearing a gown (76%, data not shown). In general, responses in the 2 interviews showed little variation in infection control precautions.
Our results indicate that healthcare workers in this study reliably recalled contact practices, patient care activities, and infection control precautions 5 months after their initial interview and 6 months after exposure to a patient with SARS. The proportion of identical follow-up responses averaged >85% for contact practices, patient care activities, and infection control precautions. Agreement between initial and follow-up responses was good to excellent for most respiratory practices and airway management activities, routine patient care activities, and other medical procedures.
The lowest proportion of identical responses observed on the initial and follow-up interview was for being in the patient’s room while the patient was coughing or spitting (59%), with a kappa value (0.38) indicating fair agreement. The risk of droplet and airborne spread of communicable diseases is assumed to be greater if a patient is frequently coughing. Hence, different infection control precautions have been recommended when caring for patients who are coughing (7). However, our results suggest that recollection of contact during this activity may not be reliable. Whether this poor reliability is related to the effect of time on memory or the intermittent nature of coughing is unclear.
The inferences that can be drawn from this study are limited by the relatively small size of our cohort. Caring for patients with SARS can be a memorable and frightening event (8,9), and recall reliability in our study may not be generalized to other clinical situations. Furthermore, the similarities among questions during the 2 interviews may have resulted in the potential for recall bias, causing an overestimation of reliability within respondents (10). Finally, our study measured the reliability rather than the validity of healthcare worker recall for determining exposure risk. Nonetheless, our findings that healthcare workers reliably recalled exposure after several months following the event should be reassuring to investigators studying risk factors for SARS transmission in hospitals and to infection control practitioners assessing exposure to communicable diseases.
Ms. Dimoulas is an epidemiologist with the Infectious Diseases Control Division of the Regional Municipality of York, Ontario, Canada. Her research interests include infectious disease surveillance and response.
This study was supported by grants from the Ontario Ministry of Health and Long Term Care and Health Canada.
- Varia M, Wilson S, Sarwal S, McGeer A, Gournis E, Galanis E, Investigation of a nosocomial outbreak of severe acute respiratory syndrome (SARS) in Toronto, Canada. CMAJ. 2003;169:285–92.
- Loeb M, McGeer A, Henry B, Ofner M, Rose D, Hlywka T, SARS among critical care nurses, Toronto. Emerg Infect Dis. 2004;10:251–5.
- Scales DC, Green K, Chan AK, Poutanen SM, Foster D, Nowak K, Illness in intensive-care staff after brief exposure to severe acute respiratory syndrome. Emerg Infect Dis. 2003;9:1205–10.
- Seto WH, Tsang D, Yung RW, Ching TY, Ng TK, Ho M, Effectiveness of precautions against droplets and contact in prevention of nosocomial transmission of severe acute respiratory syndrome (SARS). Lancet. 2003;361:1519–20.
- Landis RJ, Koch GG. The measurement of observer agreement for categorical data. Biometrics. 1977;33:159–74.
- LeDell K, Muto CA, Jarvis WR, Farr BM. SHEA guideline for preventing nosocomial transmission of multidrug-resistant strains of Staphylococcus aureus and Enterococcus. Infect Control Hosp Epidemiol. 2003;24:639–41.
- Fowler RA, Guest CB, Lapinsky SE, Sibbald WJ, Louie M, Tang P, Transmission of severe acute respiratory syndrome during intubation and mechanical ventilation. Am J Respir Crit Care Med. 2004;169:1198–202.
- Hawryluck L, Gold WL, Robinson S, Pogorski S, Galea S, Styra R. SARS control and psychological effects of quarantine, Toronto, Canada. Emerg Infect Dis. 2004;10:1205–12.
- Maunder R, Hunter J, Vincent L, Bennett J, Peladeau N, Leszcz M, The immediate psychological and occupational impact of the 2003 SARS outbreak in a teaching hospital. CMAJ. 2003;168:1245–51.
- Rothman KJ, Greenland S. Modern epidemiology. 2nd ed. Boston: Lippincott Williams and Wilkins; 1998.
- Table 1. Characteristics of healthcare workers and severe acute respiratory syndrome (SARS) index patient contact
- Table 2. Reliability of healthcare worker recalling presence in a SARS patient’s room during patient care activities
Suggested citation for this article: Dimoulas P, Green KA, Shigayeva A, Aquino M, McGeer A, Scales DC, et al. Patient contact recall after SARS exposure. Emerg Infect Dis [serial on the Internet]. 2005 Apr [date cited]. Available from http://wwwnc.cdc.gov/eid/article/11/4/04-0648
1B. Henry (Toronto Public Health), S. Paton (Health Canada), T. Stewart (Mount Sinai Hospital), D. Zoutman (Kingston General Hospital), J.M. Raboud and U.R. Saskin (Mount Sinai Hospital), M. Loeb (Hamilton Health Sciences Center), A.E. Simor and M. Vearncombe (Sunnybrook and Women’s College Hospital), C. MacDonald (Centers for Disease Control and Prevention), E. Bontovics (Ontario Ministry of Health and Long Term Care)
Please use the form below to submit correspondence to the authors or contact them at the following address:
Allison McGeer, Room 1460, Mount Sinai Hospital, 600 University Avenue, Toronto, M5G 1X5, Canada; fax: 416-586-3140
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: May 23, 2011
- Page last updated: May 23, 2011
- Page last reviewed: May 23, 2011
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)