Papers

Haematological manifestations in patients with severe acute respiratory syndrome: retrospective analysis

BMJ 2003; 326 doi: https://doi.org/10.1136/bmj.326.7403.1358 (Published 19 June 2003) Cite this as: BMJ 2003;326:1358
  1. Raymond S M Wong, haematologist,
  2. Alan Wu, medical and health officer,
  3. K F To, associate professor,
  4. Nelson Lee, medical and health officer,
  5. Christopher W K Lam, professor,
  6. C K Wong, associate professor,
  7. Paul K S Chan, associate professor,
  8. Margaret H L Ng, associate professor,
  9. L M Yu, statistician,
  10. David S Hui, associate professor,
  11. John S Tam, professor,
  12. Gregory Cheng, associate professor,
  13. Joseph J Y Sung, professor (joesung{at}cuhk.edu.hk)
  1. Department of Medicine and Therapeutics, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong Special Administrative Region, China
  2. Department of Anatomical and Cellular Pathology, Chinese University of Hong Kong
  3. Department of Chemical Pathology, Chinese University of Hong Kong
  4. Department of Microbiology, Chinese University of Hong Kong
  5. Centre for Clinical Trials and Epidemiological Research, Chinese University of Hong Kong
  1. Correspondence to: J J Y Sung
  • Accepted 23 May 2003

Abstract

Objectives To evaluate the haematological findings of patients with severe acute respiratory syndrome (SARS).

Design Analysis of the demographic, clinical, and laboratory characteristics of patients with SARS.

Setting Prince of Wales Hospital, Hong Kong.

Subjects All patients with a diagnosis of SARS between 11 March and 29 March 2003 who had no pre-existing haematological disorders.

Main outcome measures Clinical end points included the need for intensive care and death. Univariate and multivariate analyses were performed to examine factors associated with adverse outcome.

Results 64 male and 93 female patients were included in this study. The most common findings included lymphopenia in 153 (98%) of the 157 patients, neutrophilia in 129 (82%), thrombocytopenia in 87 patients (55%), followed by thrombocytosis in 77 (49%), and isolated prolonged activated partial thromboplastin time in 96 patients (63%). The haemoglobin count dropped by more than 20 g/l from baseline in 95 (61%) patients. Four patients (2.5%) developed disseminated intravascular coagulation. Lymphopenia was shown in haemato-lymphoid organs at postmortem examination. Multivariate analysis showed that advanced age and a high concentration of lactate dehydrogenase at presentation were independent predictors of an adverse outcome. Subsets of peripheral blood lymphocytes were analysed in 31 patients. The counts of CD4 positive and CD8 positive T cells fell early in the course of illness. Low counts of CD4 and CD8 cells at presentation were associated with adverse outcomes.

Conclusions Abnormal haematological variables were common among patients with SARS. Lymphopenia and the depletion of T lymphocyte subsets may be associated with disease activity.

Footnotes

  • Embedded Image

  • We thank the Haematology Division of the Department of Anatomical and Cellular Pathology for their full support in the laboratory investigations.

  • Contributors JJYS is guarantor and was responsible for patient management and coordinated the study. RSMW and GC were responsible for the study design, analysis, and writing of the paper. AW, NL, and DSH were responsible for patient management and data collection. KFT was responsible for postmortem examinations. MHLN, CWKL, and CKW were responsible for the haematological laboratory tests. PKSC and JST were responsible for the virological studies. LMY was responsible for the statistical analysis.

  • Funding None.

  • Competing interests None declared.

  • Ethical approval The study was approved by the ethics committee of the Department of Medicine and Therapeutics, Prince of Wales Hospital, Chinese University of Hong Kong.

  • Accepted 23 May 2003
View Full Text

Sign in

Log in through your institution

Free trial

Register for a free trial to thebmj.com to receive unlimited access to all content on thebmj.com for 14 days.
Sign up for a free trial

Subscribe