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. 2003 Dec 12;362(9400):2025–2026. doi: 10.1016/S0140-6736(03)15036-2

Treatment of severe acute respiratory syndrome in health-care workers

Hsin-Yun Sun a, Chi-Tai Fang a, Jann-Tay Wang a, Yee-Chun Chen a, Shan-Chwen Chang a
PMCID: PMC7124665  PMID: 14683674

Sir

There is still no proven therapy for severe acute respiratory syndrome (SARS). The protocol reported by Loletta So and colleagues1 emphasised the combination use of ribavirin and high-dose cortico-steroid. However, if given very early in the course of the disease, this approach could suppress the generation of host immunity to the novel coronavirus. We observed a biphasic pattern of illness in SARS and postulated that the first stage represents a viraemic phase and the second phase is an immune phase.2 Acute respiratory distress syndrome seems to be a complication in the second phase.2 If this hypothesis is true, antiviral agents will be most beneficial in the first phase, whereas corticosteroids should be delayed until the onset of the second phase to maximise benefit and keep the negative effects of immune suppression to a minimum.

We, therefore, developed a treatment protocol3 that emphasises early use of ribavirin but delayed introduction of corticosteroids until the second week, if possible. One oral 2000 mg loading dose of ribavirin was given to patients as soon as they received medical attention, followed by 600 mg ribavirin twice daily for patients with a bodyweight greater than 75 kg or 1000 mg daily for those with a bodyweight of 75 kg or less (400 mg in morning, 600 mg in evening) for 10 days. For patients who developed pneumonia, intravenous methylprednisolone (2 mg/kg daily for 5 days) was started on day 8 of fever or later. If rapid deterioration occurred before day 8, steroid treatment was started upon development of dyspnoea. If respiratory distress was not responsive to this dose, 500 mg methylprednisolone daily for 3 days was given. Upon improvement, the dose of steroid was tapered off over the next 2 weeks as recovery warranted.

In Taipei between April 23 and May 31, 2003, 17 health-care workers at our hospital contracted SARS.4 PCR of serum or nasopharyngeal swab proved positive in seven of the 17 health-care workers, and convalescent serum antibodies were positive in 13 health-care workers. All 17 health-care workers received our treatment protocol (table ). The median starting day of ribavirin was day 2 of fever (range 1–7 days). Only one health-care worker needed subsequent intubation and respiratory support. All 17 individuals recovered without major sequelae or subsequent relapse. With prompt identification and early treatment, mortality from SARS can be avoided among previously healthy health-care workers.

Table.

Characteristics and timing of treatment for 17 health-care workers with SARS

Age (years)/sex/occupation Protection used SARS category Ribavirin started* Steroid started Minipulse started ICU stay Maximum oxygen demand Discharge
Patient number
1 33/M/doctor N95 mask Probable D1 D7 No Room air D24
2 28/F/nurse N95 mask Suspected D2 No Room air D18
3 26/F/nurse N95 mask Probable D3 D9 No Room air D28
4 45/F/nurse N95 mask Probable D3 D10 No Nasal cannula 3 L/min D27
5 26/F/nurse N95 mask Probable D2 D8 D13 No Nasal cannula 2 L/min D28
6 49/F/register Surgical mask Probable D2 D6 D15 Yes Intubated with FiO2 0·6 D52
7 51/F/porter Surgical mask Probable D7 D13 No Nasal cannula 3 L/min D33
8 49/F/porter Surgical mask Probable D4 D7 No Nasal cannula 3 L/min D25
9 34/M/doctor N95 mask Suspected D6 No Room air D6
10 53/F/doctor N95 mask Suspected D2 No Room air D14
11 41/F/nurse N95 mask Probable D1 D10 No Room air D20
12 27/F/nurse N95 mask Suspected D4 No Room air D10
13 35/F/nurse N95 mask Probable D2 D9 No Room air D20
14 28/F/nurse N95 mask Suspected D3 No Room air D12
15 30/F/doctor N95 mask Probable D2 D8 No Room air D26
16 42/M/technician N95 mask Probable D2 D11 No Nasal cannula 3 L/min D29
17 57/F/porter N95 mask Probable D3 D13 No Room air D23

F=female. M=male. D=day since onset of fever. ICU=intensive care unit; FiO2=fractional concentration of oxygen in inspired gas.

*

Oral ribavirin 2000 mg loading then 600 mg twice daily.

Intravenous methylprednisolone 2 mg/kg daily.

Intravenous methylprednisolone 500 mg daily.

References

  • 1.So LK, Lau AC, Yam LY. Development of a standard treatment protocol for severe acute respiratory syndrome. Lancet. 2003;361:1615–1617. doi: 10.1016/S0140-6736(03)13265-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.JT Wang, JL Wang, CT Fang, SC Chang: Temporary defervescence in the first week of disease course does not indicate recovery of disease in a patient with severe acute respiratory syndrome. Emerg Infect Dis (in press).
  • 3.Department of Internal Medicine Guidelines for management of severe acute respiratory syndrome (SARS) http://ntuh.mc.ntu.edu.tw/med/sars (accessed Oct 5, 2003).
  • 4.WHO Case definitions for surveillance of severe acute respiratory syndrome (SARS) http://www.who.int/csr/sars/casedefinition/en (accessed Oct 22, 2003).

Articles from Lancet (London, England) are provided here courtesy of Elsevier

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