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. 2021 Feb 1;147(2):e2020010066. doi: 10.1542/peds.2020-010066

TABLE 4.

Responses Regarding CP Diagnosis in 4 Hypothetical Patient Scenarios

Scenariosa With Responses and Rationaleb No. Respondents %
S1: Nonprogressive spastic diplegia after premature birth
 Would diagnose CP 316 96
 Would not diagnose CP 14 4
  R1: additional imaging required 9 3
  R2: alternate diagnosis offered 4 1
S2: Progressive spastic diplegia
 Would diagnose CP 25 8
 Would not diagnose CP 305 92
  R1: progressive phenotype 278 84
  R2: alternate diagnosis offered 26 8
S3: Nonprogressive spastic diplegia with genetic etiology
 Would diagnose CP 220 67
 Would not diagnose CP 110 33
  R1: genetic 88 27
  R2: practical diagnosisc 7 2
S4: Nonprogressive hypotonia with genetic etiology
 Would diagnose CP 153 46
 Would not diagnose CP 177 54
  R1: genetic 107 32
  R2: hypotonia 39 12
  R3: practical diagnosis 8 2
a

Each scenario (S) presented in the survey (Table 1).

b

The respondent provided rationale (R) for not diagnosing CP in each scenario.

c

The respondent indicated they would not typically provide a diagnosis of CP but might consider providing one if it served a practical purpose for the patient (eg, explaining the diagnosis to the school district or gaining access to services).