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Emerg Med J 25:635-639 doi:10.1136/emj.2007.056689
  • Original Article

Derivation of a risk assessment tool for emergency department patients with sickle cell disease

Table 3 Scoring system and diagnostic test characteristics of the score and physician judgement in the validation set, 95% CI are shown
Risk factor Score if present
SS, SC, other or unknown variant +1
Chest pain +1
Chills +1
Pain not similar to previous episodes +1
Temperature <36°C or >38°C +1
Oxygen saturation <95% +1
Haemoglobin <10 +1
Nitrites present on urinalysis +1
Abnormalities observed on chest x ray +1
Total possible score 9
Score >2 Score >4 Physician judgement
Overall accuracy 61.7 (54.8 to 68.2) 82.7 (76.8 to 87.4) 81.8 (75.8 to 86.6)
Sensitivity 86.0 (73.7 to 93.3) 49.1 (35.8 to 62.6) 77.2 (63.8 to 86.8)
Specificity 52.9 (44.8 to 60.8) 94.9 (89.9 to 97.6) 83.4 (76.5 to 88.7)
False negative rate 14.0 (6.7 to 26.3) 50.9 (37.4 to 64.2) 22.8 (13.2 to 36.2)
False positive rate 47.1 (39.2 to 55.2) 5.1 (2.4 to 10.1) 16.6 (11.3 to 23.5)
Positive predictive value 39.8 (31.2 to 49.1) 77.8 (60.4 to 89.3) 62.9 (50.4 to 73.9)
Negative predictive value 91.2 (82.9 to 95.9) 83.7 (77.3 to 88.6) 91.0 (84.8 to 94.9)
  • SC, sickle cell haemogoblin C disease; SS, homozygous sickle cell disease.

  • SC, sickle cell haemogoblin C disease; SS, homozygous sickle cell disease.

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