Severe acute respiratory syndrome (SARS) has caused a major epidemic worldwide. A novel coronavirus is deemed to be the causative agent. Early diagnosis can be made with reverse transcriptase-polymerase chain reaction (RT-PCR) of nasopharyngeal aspirate samples. We compared symptoms of 156 SARS-positive and 62 SARS-negative patients in Hong Kong; SARS was confirmed by RT-PCR. The RT-PCR–positive patients had significantly more shortness of breath, a lower lymphocyte count, and a lower lactate dehydrogenase level; they were also more likely to have bilateral and multifocal chest radiograph involvement, to be admitted to intensive care, to need mechanical ventilation, and to have higher mortality rates. By multivariate analysis, positive RT-PCR on nasopharyngeal aspirate samples was an independent predictor of death within 30 days.

We devised a method for self-obtaining nasopharyngeal specimens. Patients were given detailed written or verbal instructions. Materials included a 5-ml syringe filled with injectable normal saline, a specimen container, and facial tissues. The process involved the application of normal saline eye drops and expectoration of irrigate that ran into the throat.Anatomically, the conjunctival sac is connected to the nasal cavity by the nasolacrimal duct. Contraction of the palpebral fibers of the orbicularis oculi muscles during blinking opens the normally collapsed, elastic, lacrimal sacs, which return to their collapsed state after blinking; secretions are sucked in through the lacrimal cannaliculi and discharged into the nasolacrimal ducts (1, 2). The mucosal folds in the nasolacrimal ducts ensure one-way traffic to the nose. The lipid content of the meibomian gland secretions makes the lid margins water repellant. Unless too much is applied, the irrigate does not spill from the conjunctival sacs. These anatomical features are exploited in the technique of conjunctiva-upper respiratory tract irrigation (CURTI). With this technique, patients self-apply 1 drop of normal saline per eye at a time. They are asked to blink repeatedly, tilt their heads backward, and sniff to facilitate the drainage of fluid into the nasopharynx. Patients must not swallow the liquid; instead, it should be spat into a specimen container. Patients are told that there is a time lag of up to a minute or two before the fluid begins to run into the throat, and that after one stops applying the eye drops, fluid will continue to run into the throat for a minute or two. Fluid that drains into the throat even after stopping the eye drops should be collected. Specimens reported to be salty were deemed adequate.We tested CURTI with four patients with confirmed severe acute respiratory syndrome (SARS) soon after admission. By using an immunofluorescence assay for SARS coronavirus (4), all patients were found to have seroconverted 13 to 21 days after admission (titer rose from Ͻ25 to 200 to 1,600). When real-time PCR (3) and primers Cor-1 and Cor-2 (5) were used, two of the four patients tested positive for the CURTI specimens. By comparison, none of the nose/throat swab (NTS) and stool specimens were positive.Although we cannot compare the sensitivity of CURTI with that of nasopharyngeal aspiration (NPA) since the use of NPA was rejected in our hospital, we found CURTI to be more sensitive than NTS in the four patients we studied. Analysis of data (ongoing) revealed an unsatisfactory sensitivity of 60% with NTS in confirmed cases of SARS (based on seroconversion). CURTI, therefore, has a potential sensitivity in excess of 60%.CURTI is simple and well tolerated, as shown by the results with our volunteers. It compares favorably with NPA and NTS in terms of patient comfort and staff safety because it does not provoke sneezing. The CURTI process irrigates the nasopharynx, whereas saliva comes mostly from the three pairs of salivary glands which drain into...

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Eight general practitioners had severe acute respiratory distress syndrome (SARS) in Hong Kong during the epidemic, and others may have been infected by the SARS coronavirus without developing the full syndrome. We conducted a serological and questionnaire survey to determine the prevalence of subclinical infection by SARS coronavirus among general practitioners in Hong Kong. Participants had to be doctors actively practising in family medicine and who did not have SARS. Approximately 3200 general practitioners were invited to participate and the results of 574 were eligible for analysis. 29 samples were tested positive by enzyme-linked immunosorbent assay, but all these samples had titre < 25 by immunoflorescence assay. The prevalence for seropositivity was thus 0% (95% CI, 0.0%-0.6%). This finding documents the lack of subclinical infection by SARS coronavirus in an at-risk group in the community.

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