Volume 11, Number 2—February 2005
Quarantine for SARS, Taiwan
During the 2003 outbreak of severe acute respiratory syndrome (SARS) in Taiwan, >150,000 persons were quarantined, 24 of whom were later found to have laboratory-confirmed SARS-coronavirus (SARS-CoV) infection. Since no evidence exists that SARS-CoV is infective before the onset of symptoms and the quarantined persons were exposed but not symptomatic, we questioned the quarantine’s effectiveness. Using the SARS Taiwan quarantine data, we found that the onset-to-diagnosis time of previously quarantined confirmed case-patients was significantly shortened compared to that for those who had not been quarantined. Thus, quarantine for SARS in Taiwan screened potential infective persons for swift diagnosis and hospitalization after onset, thereby indirectly reducing infections. Full-scale quarantine measures implemented on April 28 led to a significant improvement in onset-to-diagnosis time of all SARS patients, regardless of previous quarantine status. We discuss the temporal effects of quarantine measures and other interventions on detection and isolation as well as the potential usefulness of quarantine in faster identification of persons with SARS and in improving isolation measures.
The severe acute respiratory syndrome (SARS) epidemic from November 2002 to June 2003 came with much public attention and left swiftly, resulting in >8,000 probable cases worldwide and 774 deaths (1). Prominent among retrospective analyses is the belief that the simple ancient system of placing persons suspected of being infected under quarantine was instrumental in the quick containment of the outbreak (2–5). However, questions persist regarding how quarantine worked to control this disease, given the time-tested axiom that quarantine is most useful only when patients are infectious before becoming symptomatic, thus directly preventing secondary infections (6). Moreover, due to early confusion resulting from imprecise clinical diagnosis and case definition (7), correct clinical diagnosis and prompt isolation were often impossible, which resulted in insufficient isolation and gaps in the containment strategy for hospital infection control (8). Since all available evidence indicates that SARS patients were only infectious after symptom onset (9), one may argue that quarantine provides a window of several days during which illnesses can be diagnosed swiftly and persons isolated accordingly. In this study, we used data from the Taiwan SARS outbreak to explore whether quarantine was effective in expediting the time from onset to clinical diagnosis and hospitalization, and the time from clinical diagnosis to classification as a probable case-patient.
During the outbreak of 2003, 346 SARS cases were officially confirmed in Taiwan, among which were 37 direct SARS deaths and 36 SARS-related deaths as reported by the World Health Organization (WHO) (1). To guard against the potential threat of a large-scale epidemic, the government attempted to place more than 150,000 people under home quarantine. Two distinct levels of quarantine were implemented in Taiwan. Level A quarantine, aimed at people having close contact with a suspected SARS case, was implemented on March 18, 2003. Level B quarantine, aimed at travelers from affected areas, was implemented on April 28, in the aftermath of the first SARS death on April 26 (10,11). Most of the quarantined persons were confined to their homes for 10–14 days. Public health nurses would bring the quarantined persons 3 meals every day and sometimes helped them with odd jobs such as washing clothes or taking care of pets. CDC-Taiwan officially confirmed 346 SARS-CoV(+) cases, of which 17 case-patients had been previously quarantined, and 134 additional laboratory-confirmed SARS cases with Ab(+), of which 7 case-patients had previously been quarantined. The total number of confirmed SARS case-patients in Taiwan by the end of September 2004 was 480, of which 24 had been quarantined previously. Details regarding the persons quarantined during the SARS outbreak are itemized in Table 1.
The 134 patients with laboratory-confirmed SARS either had milder symptoms and SARS was therefore clinically diagnosed as suspected or ruled out at the time of the outbreak, or were patients with probable cases whose specimens had previously tested negative by PCR or anti-SARS-CoV antibody (Ab), due to wrong timing, but later were reconfirmed by >2 different laboratory tests in a follow-up epidemiologic study. Seven people in this group had been previously quarantined. Our criterion for a quarantined person was someone who had been placed under official quarantine for >1 day before the onset of symptoms. Thus, persons in whom symptoms developed on the same date or before the notification of quarantine were considered not quarantined and were therefore excluded. Persons who were known to have had a record of close contacts with others during the supposed quarantine period were also excluded. One of the 24 case-patients actually had an imported case but was quarantined before implementation of level B quarantine on April 28 for reasons other than simply being a traveler from an affected area.
We compared the mean time from onset of symptoms to clinical diagnosis (and admission) for the 24 patients with laboratory-confirmed SARS-CoV(+) who had been quarantined before symptom onset to that of the 451 SARS-CoV(+) case-patients who had not. Note that 5 cases were deleted from the data of 480 total cases for our comparison test due to missing information on their relevant dates. (We will use the term “diagnosis” to mean clinical diagnosis hereafter.) For the mean time from diagnosis to classification as probable case, we only used the officially confirmed cases for comparison, since the laboratory confirmed cases were either ruled out cases or classified as suspected cases only, and thus had no classification of probable time. Again, 2 of these cases were deleted from the data for our comparison test due to missing information on their relevant dates; therefore, 344 case-patients (17 quarantined and 327 nonquarantined) were used. Due to the skewed data, we used the nonparametric Mann-Whitney test.
To investigate the effect of large-scale quarantine on the changes in the efficiency of the public health system to identify SARS patients for isolation, we considered the temporal effect of important events for intervention and control of SARS in Taiwan. On April 28, level B quarantine was implemented, which marked the start of large-scale home quarantine (12).
A second important date in SARS prevention and control was May 10, when changes in the review and classification procedures were implemented by the cabinet-level SARS Prevention and Extrication Committee in Taiwan to expedite the review and classification of SARS cases (13). Before May 9, the relevant medical records (including any available laboratory test results) of all reported SARS patients were reviewed by a central SARS Advisory Committee of the Center for Disease Control (CDC)–Taiwan in Taipei. Due to the rapid increase in the number of reported cases caused by the hospital cluster outbreaks in Taipei in late April, the SARS Advisory Committee in CDC-Taiwan could not handle the rapidly increasing caseload. Consequently, after May 10, 3 regional offices of the Bureau of National Health Insurance in northern, central, and southern Taiwan took over the responsibility of case review. Local SARS expert committees were established in the 3 regions with each committee consisting of specialists similar to the central committee in Taipei. The experiences and the standard operation procedures of case review and case classification used by the central committee were transferred to the 3 regional SARS expert committees in the Bureau of National Health Insurance through several consensus meetings (14).
We used the Mann-Whitney test to compare the time intervals from onset to clinical diagnosis of SARS symptoms of the patients with confirmed SARS-CoV(+) case-patients with onset occurring during the 3 periods of February 25–April 27 (period 1), April 28–May 9 (period 2), and May 10–June 15 (period 3). Five patients were deleted from the data for our comparison test due to missing information on their relevant dates, and 2 patients were deleted because their onsets of SARS did not occur during the 3 time periods.
We also compared, using the Mann-Whitney test, the intervals from diagnosis to classification as probable SARS of the 343 officially confirmed SARS-CoV(+) case-patients with the time taken to classify suspected SARS. Again, the laboratory-confirmed cases had never been classified as probable cases. Moreover, 2 cases were deleted from the data for our comparison test due to missing information on their relevant dates, and 1 case was deleted because classification as a probable case-patient did not occur during the 3 periods from February 25 to June 15..
The mean time from onset to diagnosis for the previously quarantined persons (1.20 days) was significantly shorter than that of those who were not quarantined (2.89 days) (Table 2). However, the respective mean times from diagnosis to classification (6.21 days and 7.34 days) (Table 2), though slightly reduced for the quarantined persons, were not significantly different. For the mean onset-to-diagnosis time, period 1 took significantly longer (3.60 days to 2.49 days) than period 2 (p<0.0001), while the mean difference before and after May 10 was not significant (p = 0.0722) (Table 3). The mean diagnosis-to-classification time (Table 4) was not significantly different from period 1 to period 2. However, the time was significantly shortened after May 10 (from period 2 to period 3).
Discussion and Conclusions
The experience in the affected areas has shown that the transmission of SARS can be prevented by adherence to basic public health measures, including rapid case detection, isolation of patients with suspected and probable cases, contact tracing, and good infection control (9).The effect of possible delays in effective isolation of probable case-patients has been studied in some modeling work on SARS (15–17). In Taiwan, all patients were supposed to be placed in the isolation room and negative pressure room, if available, as soon as they were reported as having probable or suspected SARS. For most of May, the number of suspected case-patients alone remained well above 1,000, partly because of confusion in diagnosis and the tendency to overdiagnosis due to heightened alertness on the part of physicians and legal punishment for underreporting. At times, however, due to lack of available isolation rooms or simply due to the sheer number of suspected cases pending review, patients with suspected but unconfirmed SARS were kept for days in an observation room or emergency department under crude isolation, where nosocomial infections readily occurred. At other times, patients scheduled to transfer to another hospital with negative pressure isolation rooms were temporarily kept in the observation room in the emergency department where nosocomial infections might occur because of insufficient isolation and protection procedures (18). When full isolation facilities were not available to all patients, those classified as probable SARS case-patients likely received higher priority and were observed during their isolation with a higher state of alertness by healthcare workers than were the suspected case-patients.
For some case-patients, delays had occurred due to the patient’s uncertain status or urgent need for intubation without comprehensive information on the patient’s contact and clinical history; these delays led to insufficient protection and isolation. One well-known case-patient was the index patient at Hoping Hospital in Taipei, where the largest cluster infection in Taiwan occurred. Her condition was diagnosed and reported as suspected SARS on April 9. However, because the patient had no apparent contact with another known SARS case-patient, her case was reviewed but not reclassified as probable until April 25, by which time the clustered cases, which included medical staff members who took care of her and an x-ray technician who took her x-rays, had already forced the hospital to be shut down on the previous day. Surely more strict infection control would have been in place had the index patient been confirmed as a probable SARS patient. Several other similar cases occurred in Taiwan, some well over 1 month later. Therefore the importance of rapid classification as probable case-patients cannot be ignored.
Our results show that quarantine reduced the time from onset to diagnosis, but did not significantly reduce the time from diagnosis to classification. Thus, a previously quarantined person could expect his or her condition to be diagnosed and to be hospitalized more quickly once clinical symptoms appeared. However the same person would not receive higher priority in the classification process to determine candidates for effective isolation. Nevertheless, in many hospitals with available isolation rooms, patients with suspected cases were effectively isolated as soon as chest x-ray evidence of infiltrates consistent with pneumonia or acute respiratory distress syndrome became available. Moreover, in the latter stages of the epidemic when a reliable laboratory test for SARS-CoV(+) became more available, many patients were isolated in negative pressure chambers immediately if results of reverse transcription–polymerase chain reaction test for SARS-CoV from 2 different laboratories were positive. Therefore, the effect of classification as a probable case-patient might not as pronounced as it would have been otherwise.
For all laboratory confirmed case-patients, regardless of whether they were quarantined previously, the implementation of full-scale intervention measures, including level B quarantine on April 28, had significantly decreased the time from onset to diagnosis, but it only slightly improved the time from diagnosis to classification. However, the small sample size of 24 previously quarantined SARS case-patients did not permit a meaningful test of whether a significant difference existed for the previously quarantined persons during each of the 3 periods.
By comparison, the change in the review and classification procedure initiated on May 10 was significant in helping shorten the diagnosis-to-classification time for all SARS patients, indicating that the action by the SARS Prevention and Extrication Committee to expedite the review process had indeed worked. (However, by separating the analyses of data into discrete epochs marked by significant events, we have included those cases whose illnesses straddle epochs.)
In the future, when facing newly emerging infectious diseases like SARS, when whether the patient is infectious in the incubation period is unknown, precise clinical diagnosis is lacking, and modes of transmission are uncertain, quarantine should be used not only to directly prevent possible asymptomatic infections but also to screen out potential infective persons to swiftly prevent secondary or even tertiary infections after the symptoms appear.
The quarantine in Taiwan was indeed useful in helping identify persons who are likely to develop symptoms and isolate them more quickly if and when they did, although its effect on isolation and infection control could perhaps be improved by quicker classification or confirmation of previously quarantined patients. No conclusion was drawn regarding whether better outbreak control would be achieved by placing fewer persons in quarantine or by concentrating on improving the efficiency of detection and isolation procedures. In fact, both areas may be improved in efficiency without jeopardizing the other’s improvement.
Dr. Hsieh is a professor of applied mathematics at National Chung Hsing University. His primary research interests are focused on mathematical and statistical modeling of infectious diseases epidemiology.
We are grateful to Roy Anderson, John Glasser, and Fred Brauer for constructive discussions that helped formulate some of the ideas for this work and to the anonymous referees for their many valuable comments. Sincere thanks are also extended to central and local public health personnel and medical staff who devoted all of their efforts to the quarantine and prevention of SARS in Taiwan without complaints. Y.H.H. would like to thank MITACS for their generous financial support for Y.H.H. to attend MITACS SARS meetings at Banff, Alberta, Canada, where several of the above-mentioned discussions took place.
Y.H.H. (NSC 92-2751-B005-001-Y), C.C.K. (NSC 92-2751-B002-020-Y), and M.S.H. were supported by SARS research grants from the National Science Council of Taiwan.
- World Health Organization. Summary of probable SARS cases with onset of illness from 1 November 2002 to 31 July 2003 (revised 26 September 2003). Available at http://www.who.int/csr/sars/country/table2003_09_23/en/.
- Enserink M. SARS: a pandemic prevented. Science. 2003;302:2045.
- Ou J, Li Q, Zeng G. Efficiency of quarantine during an epidemic of severe acute respiratory syndrome—Beijing, China, 2003. MMWR Morb Mortal Wkly Rep. 2003;52:1037–40.
- Pang X, Zhu Z, Xu F, Guo J, Gong X, Liu D, Evaluation of control measures implemented in the severe acute respiratory syndrome outbreak in Beijing, 2003. JAMA. 2003;290:3215–21.
- Chau PH, Yip PSF. Monitoring the severe acute respiratory syndrome epidemic and assessing effectiveness of interventions in Hong Kong Special Administrative Region. J Epidemiol Community Health. 2003;57:766–9.
- Diamond B. SARS spread new outlook on quarantine models. Nat Med. 2003;9:1441.
- Hon KL, Li AM, Cheng FW, Leung TF, Ng PC. Personal view of SARS: confusing definition, confusing diagnoses. Lancet. 2003;361:1984–5.
- Chow KY, Lee CE, Ling ML, Heng DMK, Yap SG. Outbreak of severe acute respiratory syndrome in a tertiary hospital in Singapore, linked to an index patient with atypical presentation: epidemiological study. BMJ. 2004;328:195–8.
- World Health Organization. Consensus document on the epidemiology of severe acute respiratory syndrome (SARS). October 17, 2003. Available at http://www.who.int/csr/sars/en/WHOconsensus.pdf.
- Twu SJ, Chen TJ, Chen CJ, Olsen SJ, Lee LT, Fisk T, Control measures for severe acute respiratory syndrome (SARS) in Taiwan. Emerg Infect Dis. 2003;9:718–20.
- Lee Ml , Chen CJ, Su IJ, Chen KT, Yeh CC, King CC, et al. Use of quarantine to prevent transmission of severe acute respiratory syndrome—Taiwan 2003. MMWR Morb Mortal Wkly Rep. 2003;52:680–3.
- Hsieh YH, Lee JY, Chang HL. On SARS epidemiology, cumulative case curve, and logistic-type model: ascertaining effectiveness of intervention and predicting case number. Emerg Infect Dis. 2004;10:1165–7.
- Center for Disease Control-Taiwan. SARS major timeline. In: Memoir of severe acute respiratory syndrome control in Taiwan, 2003. Taipei: CDC-Taiwan; 2003. p. 67–81.
- Hsieh YH, Chen CWS, Hsu SB. SARS outbreak in Taiwan [reply to Hsueh and Yang]. Emerg Infect Dis. 2004;10:1515–6.
- Lloyd-Smith JO, Galvani AP, Getz WM. Curtailing transmission of severe acute respiratory syndrome within a community and its hospital. Proc R Soc Lond B Biol Sci. 2003;270:1979–89.
- Hsieh YH, Chen CWS, Hsu SB. SARS outbreak, Taiwan 2003. Emerg Infect Dis. 2004;10:201–6.
- Fraser C, Riley S, Anderson RM, Ferguson NM. Factors that make an infectious disease outbreak controllable. Proc Natl Acad Sci U S A. 2004;101:6146–51.
- Wu JS, Ho MS, Huang TM, Chen KT, Hsu KH, Su IJ, Epidemiological investigation of the SARS outbreak in the Taipei Municipal Hoping Hospital. Memoir of severe acute respiratory syndrome control in Taiwan, 2003. CDC-Taiwan: Taipei;2003. p. 45–8.
Suggested citation for this article: Hsieh Y-H, King C-C, Chen CWS, Ho M-S, Lee J-L, Liu F-C, et al. Quarantine for SARS in Taiwan. Emerg Infect Dis [serial on the Internet]. 2005 Feb [date cited]. Available from http://wwwnc.cdc.gov/eid/article/11/2/04-0190
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