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One patient dropped from the study because of severe nausea during a headache attack treated with PCF.
Only one patient withdrew from the study because of severe injection site erythema and induration.
Also none of the patients withdrew from the study because of severe pain requiring additional analgesics beyond the intravenous morphine.
Six infants were excluded from the study because of severe intraventricular hemorrhage, surgical treatment, and preterm birth at 22 wk.
The number of eligible women dropped somewhat at pregnancy week 32 and 8 weeks postpartum because some women had moved or were withdrawn from the study because of severe complications (N = 261).
Clinicians at the sites receive lists of their patients who are eligible or possibly eligible and are asked to indicate any that should be excluded from the study because of severe or terminal health conditions, behavioral health issues that precludes working with a health coach, or another reason (e.g., patient does not have phone or does not speak English or Spanish).
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Five patients were unable to complete the study because of severe nausea and vomiting and were excluded from analysis.
Two mothers discontinued the study because of severe depression.
No participant dropped out of the study because of severe post immunization reaction.
Forty-six subjects refused to participate in the study because of severe comorbidities or lack of interest.
Of these 122 participants, 28 were excluded from the study as they did not complete the questionnaire, and one participant was unable to attend the study because of severe general condition.
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