The ALGOBASES project is an observational epidemiological study of pain through the collection of pain evaluation questionnaires and information with the aim of creating a descriptive "pain" evaluation in all patients who need to benefit from orthopedic, thoracic or gynecological surgery. The painful symptomatology will thus be evaluated in all its dimensions (demographic data, physical, psychological, socio-cultural components) and linked to the pathology justifying the specialized care. It is planned to collect the same data at each subsequent event in order to allow the determination of predictive factors, pain trajectories according to the type of surgery, and the profile of subjects at risk of acute or chronic postoperative pain.
Study Type
OBSERVATIONAL
Descriptive analysis of the typology of pain in patients needing surgery.
The typology of pain will be analyzed on the basis of responses to questionnaires on the affective and sensory dimension of pain, quality of life, depression, anxiety and catastrophizing
Time frame: Baseline
Descriptive analysis of specific symptomatology of pain Description of the general and painful symptomatology in patients needing surgery.
Describe the specific symptomatology of pain separately according to the 3 pathologies: patients needing orthopedic, thoracic and gynecological surgery.
Time frame: follow-up over a period of five years during post-operative or pain medical consultation
Pain Catastrophizing Scale (PCS) according to pain
Time frame: Baseline and follow-up over a period of five years during post-operative or pain medical consultation
Hospital Anxiety Depression scale (HAD) according to pain
Time frame: Baseline and follow-up over a period of five years during post-operative or pain medical consultation
EQD5 according to pain
Time frame: Baseline and follow-up over a period of five years during post-operative or pain medical consultation
Identification of factors predictive of acute or chronic pain.
The presence of pain will be defined by the presence of severe pain and/or the presence of neuropathic pain.
Time frame: Baseline and at three months, six months, one year
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