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. 2015 Jun 25;61(5):800–806. doi: 10.1093/cid/civ495

Table 3.

Overall Clinical Outcome for the SCOUT-CAPa Trial (From Most to Least Desirable)

  1. Survival; adequate clinical response; no adverse events

  2. Survival; adequate clinical response; mild adverse event(s)

  3. Survival; adequate clinical response; moderate adverse event(s)

  4. Survival; adequate clinical response; severe adverse event(s)

  5. Survival; inadequate clinical response without additional emergency department or clinic visit or hospitalization

  6. Survival; inadequate clinical response with additional emergency department or clinic visit but without hospitalization; any grade of adverse event

  7. Survival; inadequate clinical response with hospitalization; any grade of adverse event

  8. Death

Adequate clinical response was defined based on absence of all of the following as assessed on day 11–14 after initiation of therapy: (1) fever unless related to a new process that is unrelated to the prior diagnosis of pneumonia, (2) tachypnea, (3) increased work of breathing (retractions, nasal flaring, grunting), and (4) a medically attended visit to an emergency department/clinic or hospitalization for persistent or worsening pneumonia at any time after randomization. This is a draft version from a developing clinical trial.

a Short-Course Outpatient Therapy for Community-Acquired Pneumonia in Children.