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Mortality and neurological morbidity were evaluated; the children had neurodevelopmental follow-up with a mean follow-up time of 24 months.
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Morbidity was evaluated through record-linkage between GPs' data records and hospital admissions happened in year 2006, in order to assess the occurrence of previous illnesses that could be associated with the likelihood of being identified by GPs as frail or pre-frail.
In this second part of the study, the experimental performance of the previously analysed models in predicting the risk of morbidity is evaluated in a real clinical scenario.
Current psychological morbidity was evaluated from the General Health Questionnaire-12-item version (GHQ-12), 25 26 a non-specific screening tool for psychological morbidity which measures anxiety, loss of self-confidence and social dysfunction.
Neonatal morbidity and mortality were evaluated.
Indicators of maternal morbidity and mortality were evaluated for the three age groups.
To begin our analyses, we inoculated male and female C57BL/6 mice with IAV and morbidity and mortality were evaluated over a 21-day period in gonadally intact WT mice that were older than in previous studies [ 32] (that is, animals were 18-22 weeks of age to be age matched to FCG mice).
The proportions of invalid (false positive) and missed links (false negatives) between Western Australian hospital morbidity and mortality databases were evaluated several years ago, and both false positives and negatives were estimated to be 0.11% [20].
Other co-morbidities and co-medications were evaluated based on open questions.
Morbidity, survival, and recurrence rate were evaluated.
Changes in morbidity, PCP, or diabetes treatment were evaluated for impact on outcomes.
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