Emerg Infect DisEmerging Infect. DisEIDEmerging Infectious Diseases1080-60401080-6059Centers for Disease Control and Prevention15714659329434504-064510.3201/eid1101.040645Letters to the EditorLetterSARS-CoV Sampling from 3 PortalsSARS-CoV Sampling from 3 PortalsTongTommy R.*Princess Margaret Hospital, Hong Kong, Special Administrative Region, ChinaAddress for correspondence: Tommy R Tong, Department of Pathology, Room P-725, Block P, 7/F, Princess Margaret Hospital, Kowloon, Hong Kong; fax: +852-29903377; email: tommy.tong@members.nyas.org12005111167167WangWK , ChenSY , LiuIJ , ChenYC , ChenHL , YangCF , Detection of SARS-associated coronavirus in throat wash and saliva in early diagnosis.Emerg Infect Dis. 2004;10:12139.15324540Keywords: letterSARSSARS-CoVsalivatearconjunctiva

To the Editor: Wang et al. detected severe acute respiratory syndrome–associated coronavirus (SARS-CoV) from throat wash and saliva specimens and suggested that these specimens have advantages over other specimens, including ease of procurement and safety for medical personnel (1). The virus has been detected with variable success from nasopharyngeal aspirates, nose and throat swabs, and tears (2,3). Advocates of all of these sampling methods emphasize the need for early diagnosis of SARS. The probability for nosocomial transmission to healthcare workers when they obtain specimens from patients has not been adequately addressed. In a study of outbreak control for SARS, Chowell et al. suggest “… the strong sensitivity of R0 to the transmission rate β indicates that efforts in finding intervention strategies that manage to systematically lower the contact rate of persons of all age groups promise an effective means for lowering R0” (4).

An important component of a comprehensive strategy to lower the contact rate is improving the safety measures recommended for clinical specimen collection by healthcare workers. Recognizing the importance of obtaining multiple specimens and the difficulties associated with obtaining samples from the 3 usual portals of entry, we devised and tested a novel method of specimen collection, conjunctiva–upper respiratory tract irrigation (5). We coupled our specimen collection method with detailed written instructions to enable the patients themselves to perform the entire procedures. Almost all other specimen collection methods require assistance from healthcare workers or have other limitations, such as inability to sample all 3 portals. The method is not perfect because some persons have difficulty performing the procedure; however, self-instillation of the irrigation into the nostrils, with or without the addition of a throat wash or saliva, is likely to improve the success rate. The data supplied by Loon et al. (3) and Wang et al. (1) confirm that collecting specimens by a method that involves minimal contact between a possible source of infection and susceptible persons is desirable.

Suggested citation for this article: Tong TR. SARS-CoV sampling from 3 portals [letter]. Emerg Infect Dis [serial on the Internet]. 2005 Jan [date cited]. http://dx.doi.org/10.3201/eid1101.040645

The author has shares of a company that owns a patent-pending conjunctiva-upper respiratory tract irrigation system.

ReferencesWang WK, Chen SY, Liu IJ, Chen YC, Chen HL, Yang CF, Detection of SARS-associated coronavirus in throat wash and saliva in early diagnosis. Emerg Infect Dis. 2004;10:121391532454015324540Chan PK, To WK, Ng KC, Lam RK, Ng TK, Chan RC, Laboratory diagnosis of SARS. Emerg Infect Dis. 2004;10:825311520081515200815Loon SC, Teoh SC, Oon LL, Se-Thoe SY, Ling AE, Leo YS, The severe acute respiratory syndrome coronavirus in tears. Br J Ophthalmol. 2004;88:8613 10.1136/bjo.2003.0359311520522515205225Chowell G, Castillo-Chavez C, Fenimore PW, Kribs-Zaleta CM, Arriola L, Hyman JM Model parameters and outbreak control for SARS. Emerg Infect Dis. 2004;10:1258631532454615324546Tong TR, Lam BH, Ng TK, Lai ST, Tong MK, Chau TN Conjunctiva–upper respiratory tract irrigation for early diagnosis of severe acute respiratory syndrome. J Clin Microbiol. 2003;41:5352 10.1128/JCM.41.11.5352.20031460520514605205