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. Author manuscript; available in PMC: 2015 Apr 17.
Published in final edited form as: Arch Neurol. 2012 Dec;69(12):1578–1582. doi: 10.1001/2013.jamaneurol.79

Table 5.

Disease Duration and Significant Diagnosing Event

Disease Course, mo Time From First Symptoms to CJD Mentioned in the Differential, mo Time From First Symptoms to CJD “Likely” Diagnosis or Contacting UCSF, moa % of Disease Course Before Contacting UCSF or CJD Diagnosisb
Sample sizec 94 60 92 92
Mean (SD) 12.0 (10.3) 6.7 (6.5) 7.8 (6.9) 67.7 (0.2)
Median (range) 12.0 (0.8–57.7) 4.9 (0.4–39.1) 6.0 (0.9–39.2) 68.9 (18.6–99.4)

Abbreviations: CJD, Jakob-Creutzfeldt disease; UCSF, University of California, San Francisco.

a

Time used for whichever comes first: patient being referred to UCSF CJD/rapidly progressive dementia program or medical records suggesting CJD as the likely diagnosis.

b

Either probable clinical diagnosis or definite (pathology-proven) diagnosis.

c

Number of subjects available for each analysis; for 5 subjects, records were not sufficient to identify specific dates.