Cholecystectomy, Laparoscopic, Haemorrhoidal Surgery, Hernioplasty, Knee Arthroscopy, Shoulder Arthroscopy
Conditions
Keywords
Pain, Post-surgery pain, pain control
Brief summary
Moderate to severe acute postoperative pain (APP) during part of the postoperative period is a barrier that hinders the central objective of perioperative medicine, which is to achieve an optimal postoperative recovery process. Despite advances in perioperative medicine, a large proportion of post-operative patients continue to suffer from moderate to severe APS during many of the days of their convalescence. This poor control of APS, in addition to causing suffering and exposing the patient to an increased risk of complications, could impair the quality of post-surgical recovery , according to some authors. We therefore consider it to be of utmost interest in our field to corroborate whether the implementation of measures to better control DAP is related to a better quality of post-surgical recovery. Currently, the growing trend to take into account the perspective of patients in their care has prompted the development of various patient-centred measurement tools that, among other aspects, assess the quality of post-surgical recovery. Several scales have been designed. The most widely used are the QoR-40, QoR-9 and QoR-15 scales. The latter, with a range of 0 to 150, was developed to simplify assessment, especially in telephone follow-ups, and has a reliability similar to its predecessor, the QoR-40.
Interventions
OTHERIntensive monioring group
Routine follow-up (telephone call on the morning after surgery) and Intensive follow-up of acute post-surgery pain (telephone call every day since pain resolution).
Routine follow-up (telephone call on the morning after surgery).
Sponsors
Consorci Sanitari del Maresme
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients ≥ 18 years old. * ASA I - III. * Scheduled for the surgeries: Laparoscopic or open inguinal hernia repairs, Laparoscopic cholecystectomies, Haemorrhoid surgeries, Knee arthroscopies, Shoulder arthroscopies. * Willingness to be contacted by telephone during the duration of the study. * Informed written consent to participate in this study.
Exclusion criteria
* Lack of proficiency in Spanish. * Undergoing study or follow-up for moderate to severe cognitive impairment. * Pregnant or breastfeeding patients. * Patients on major opioid medication. * Patients with a history of dependence/abuse of alcohol or illicit drugs at present. * Patients under active follow-up by the chronic pain unit.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Quality of Recovery | Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery | Quality of Recovery (QoR15 test) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain Control by Visual Analogic Scale | Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery | Visual Analogic Scale of pain. Range values: 0 (minium pain) thru 10 (maximum pain) |
| Satisfaction of pain control | Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery | A 4-level Likert scale will be used according to the patient's criteria: dissatisfied, slightly dissatisfied, fairly satisfied, completely satisfied. |
| Adherence to prescribed analgesic treatment | Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery | 4-level Likert scale according to the patient's criteria: no adherence, low adherence, moderate adherence, and total adherence. |
Countries
Spain
Outcome results
None listed