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Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 2001 Sep;85(3):218–222. doi: 10.1136/adc.85.3.218

The child with a non-blanching rash: how likely is meningococcal disease?

L Wells 1, J Smith 1, V Weston 1, J Collier 1, N Rutter 1
PMCID: PMC1718924  PMID: 11517104

Abstract

AIMS—To examine a number of simple clinical features and investigations in children with a non-blanching rash to see which predict meningococcal infection.
METHODS—A total of 233 infants and children up to 15 years of age presenting with a non-blanching rash were studied over a period of 12 months. Clinical features and laboratory investigations were recorded at presentation. The ability of each to predict meningococcal infection was examined.
RESULTS—Eleven per cent had proven meningococcal infection. Children with meningococcal infection were more likely to be ill, pyrexial (>38.5°C), have purpura, and a capillary refill time of more than two seconds than non-meningococcal children. Five children with meningococcal disease had an axillary temperature below 37.5°C. No child with a rash confined to the distribution of the superior vena cava had meningococcal infection. Investigations were less helpful, although children with meningococcal infection were more likely to have an abnormal neutrophil count and a prolonged international normalised ratio. No child with a C reactive protein of less than 6 mg/l had meningococcal infection.
CONCLUSIONS—Most children with meningococcal infection are ill, have a purpuric rash, a fever, and delayed capillary refill. They should be admitted to hospital and treated without delay. Children with a non-blanching rash confined to the distribution of the superior vena cava are very unlikely to have meningococcal infection. Measurement of C reactive protein may be helpful—no child with a normal value had meningococcal infection. Lack of fever at the time of assessment does not exclude meningococcal disease.



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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alcalay J., Ingber A., Sandbank M. Mask phenomenon: postemesis facial purpura. Cutis. 1986 Jul;38(1):28–28. [PubMed] [Google Scholar]
  2. Baker R. C., Seguin J. H., Leslie N., Gilchrist M. J., Myers M. G. Fever and petechiae in children. Pediatrics. 1989 Dec;84(6):1051–1055. [PubMed] [Google Scholar]
  3. Brogan P. A., Raffles A. The management of fever and petechiae: making sense of rash decisions. Arch Dis Child. 2000 Dec;83(6):506–507. doi: 10.1136/adc.83.6.506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Carrol E. D., Thomson A. P., Shears P., Gray S. J., Kaczmarski E. B., Hart C. A. Performance characteristics of the polymerase chain reaction assay to confirm clinical meningococcal disease. Arch Dis Child. 2000 Sep;83(3):271–273. doi: 10.1136/adc.83.3.271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Kravitz P. The clinical picture of "cough purpura," benign and non-thrombocytopenic eruption. Va Med. 1979 May;106(5):373–374. [PubMed] [Google Scholar]
  6. Mandl K. D., Stack A. M., Fleisher G. R. Incidence of bacteremia in infants and children with fever and petechiae. J Pediatr. 1997 Sep;131(3):398–404. doi: 10.1016/s0022-3476(97)80065-0. [DOI] [PubMed] [Google Scholar]
  7. Marzouk O., Bestwick K., Thomson A. P., Sills J. A., Hart C. A. Variation in serum C-reactive protein across the clinical spectrum of meningococcal disease. Acta Paediatr. 1993 Sep;82(9):729–733. doi: 10.1111/j.1651-2227.1993.tb12547.x. [DOI] [PubMed] [Google Scholar]
  8. Strozik K. S., Pieper C. H., Roller J. Capillary refilling time in newborn babies: normal values. Arch Dis Child Fetal Neonatal Ed. 1997 May;76(3):F193–F196. doi: 10.1136/fn.76.3.f193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Van Nguyen Q., Nguyen E. A., Weiner L. B. Incidence of invasive bacterial disease in children with fever and petechiae. Pediatrics. 1984 Jul;74(1):77–80. [PubMed] [Google Scholar]

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