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All indications were collected regardless of whether or not the post-operative diagnosis coincided with the preoperative diagnosis.
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The drug-disease interactions (indications) are collected from CTD, which in turn, are manually curated from the literature.
Demographics, clinical data and EEG indication were collected from medical charts.
For instance, no indication was collected on the patterns of behaviour out of the two peak time zones.
Procedure-related information such as the clinical indication was collected manually from the Radiology Information System RISS) and PACS of each hospital and/or from the medical records of the patients.
Information on women's socio-demographic characteristics and indications for referral were collected.
Additionally, work-related and indication-specific variables were collected.
Demographic, physiologic, and clinical data, including age, sex, smoking history, co-morbidities, and main indication for MV, were collected.
Data on maternal and neonatal clinical factors that constitute indication for CS were collected based on primary and secondary discharge diagnoses from the Hospital Information System; information was retrieved from the hospitalization for delivery, and all hospital admissions in the previous two years.
Data on age, sex, indication and colonoscopy findings were collected.
Data on treatment indication and adverse events were collected by specialist toxicology nurses, database scientists, senior medical trainees and consultant clinical toxicologists.
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