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It is currently unknown whether the most widely accessible website information on birth after previous caesarean section is evidence-based or non-biased, and therefore reflective of the information contained within the RCOG patient information document.
Websites were assessed for their content supportive of either vaginal birth after caesarean (VBAC) or elective repeat caesarean section (ERCS), using the RCOG patient information document, 'Birth after previous caesarean; Information for You' as a 'gold standard'.
This study has revealed that the content of readily accessed websites with information on birth options after CS reflect that contained in the RCOG patient information document 'Birth after previous caesarean; information for you' to a variable extent.
We observed in a previous study that the most frequently returned websites containing information on birth options after CS provide an incomplete picture of the risks involved for each approach to birthing mode when compared to the Royal College of Obstetricians and Gynaecologists (RCOG) patient information document [ 5]; 'Birth after previous caesarean; Information for You' [ 14].
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First come the lab tests on your genes: $6000 before you even start the treatment, according to patient information documents sent by the clinic.
Patient information documents and consent forms will also be tested.
These included competencies: "Integrating patient information," "Documenting patient information," "Prioritizing drug-related problems," "Establishing monitoring parameters with patients," " Patient follow-up by phone or in-person," and "Providing basic and comprehensive pharmaceutical care".
Patients were told only about the group to which they had been assigned and were given one of the two possible patient information documents with the consent form.
Between those two extremes, evidence shows clearly greater content mastery by students in the enhanced APPE; notably in patient follow-up, integrating patient information, documenting for continuity of care, and establishing monitoring parameters.
Furthermore, the high rate we observed in our population could also be a reflection of our active information programme including patient information documents and workgroups comprising doctors, caregivers, and a jurist specialized in medical law which might have facilitated exchanges on the subject.
After this, codes were grouped into two main categories: 1) justification for the use of placebo and 2) blinding and randomisation as described in the patient-information documents [ 12].
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