Surgery Clinical Trial
Official title:
Is Life Worth Living After Major Emergency GI Surgery? Patient Reported Outcome in Elderly Emergency Surgery Patients
To study the impact of emergency high risk GI surgery on HRQOL in elderly patients, seventy-five years or above and to explore the patients' experience with the informed consent process and the status 6 months after surgery.
We will identify all patients aged ≥ 75 having an emergency GI laparotomy or laparoscopy
between the 1st of November 2014 and the 30st of April 2015.
The first part of the study will take place in the first postoperative week, while the
patient is in hospital. After consent we will ask both patient and relatives/caregivers
questions concerning the preoperative course and the informed consent. We will ask for
permission to call the patients for a followup (the second part of the study) 5-7 months
after discharge and permission to contact their closest relative. The closest relative is
chosen by the patient and will after consent be asked the same questions in the first
postoperative week and after 6 months.
The second part of the study will be initiated with a letter with SF-36 and an additional
questionnaire . The SF-36 will be returned by letter. We will contact the patients by
telephone 2 weeks after sending the letter ask them the questions from the additional
questinaire.
We will compare the results from the SF-36 with age-matched controls (Data from the Danish
SF-36 Manual).
If the patient is not capable of answering the questionnaires, the primary reason is noted
(e.g. suffering from dementia or didn't speak Danish, dead).
We will aim at a 6 month follow-up period after discharge allowing a range from 5-7 months.
Data acquisition will be done in the fall 2014 until late 2015.
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Observational Model: Cohort, Time Perspective: Prospective
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