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In the planned study the investigators want to evaluate the relation between postoperative complications and minor/ major morbidities, mortality and Mean Platelet Volume (MPV) and Neutrophil/ lymphocyte (N/L) ratio.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1 | Group 1: patients receiving general anesthesia and having a postoperative pain VAS score equal to or below 50 at 1st, 6th, 12th nd 24th hours the pain sores will be evaluated at 4 time intervals and so the number of patients in every group may change at every time interval. | ||
| Group 2 | Group 2: patients receiving general anesthesia and having a postoperative pain VAS score equal to or above 60 at 1st, 6th, 12th nd 24th hours the pain sores will be evaluated at 4 time intervals and so the number of patients in every group may change at every time interval. | ||
| Group 3 | Group 3: patients receiving regional (spinal) anesthesia and having a postoperative pain VAS score equal to or below 50 at 1st, 6th, 12th nd 24th hours the pain sores will be evaluated at 4 time intervals and so the number of patients in every group may change at every time interval. | ||
| Group 4 | Group 4: patients receiving spinal anesthesia and having a postoperative pain VAS score equal to or above 60 at 1st, 6th, 12th nd 24th hours the pain sores will be evaluated at 4 time intervals and so the number of patients in every group may change at every time interval. |
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| Measure | Description | Time Frame |
|---|---|---|
| postoperative VAS (visual analogue scale) score | postoperative visual analog scale score for pain evaluation 0,10,20,30,40,50,60,70,80,90,100) | VAS score at postoperative twenty-forth hours will be evaluated |
| Measure | Description | Time Frame |
|---|---|---|
| analgesic drugs | analgesic drugs given according to the routine practice in the ward | total dose of analgesic drugs required at twenty four hours will be evaluated |
| postoperative major morbidities |
| Measure | Description | Time Frame |
|---|---|---|
| postoperative side effects | nausea, vomiting, abdominal pain, agitation, head ache, muscular weakness, dizziness,hiccups, bronchospasm, bradycardia, itching, urinary retention, | at postoperative first, sixth, twelfth and twenty-forth hours |
Inclusion Criteria:
Exclusion Criteria:
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All consecutive patients undergoing knee arthroplasty in 3 years period with general or spinal anesthesia.
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| Name | Affiliation | Role |
|---|---|---|
| Ilker o Aycan, asso prof | Akdeniz University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| AkdenizU | Antalya | 07058 | Turkey (Türkiye) |
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| Label | URL |
|---|---|
| The role of mean platelet volume in patients with non-specific abdominal pain in an emergency department | View source |
| Neutrophil/Lymphocyte Ratio as a Predictor of In-Hospital Major Adverse Cardiac Events, New-Onset Atrial Fibrillation, and No-Reflow Phenomenon in Patients with ST Elevation Myocardial Infarction | View source |
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| ID | Term |
|---|---|
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
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postoperative Myocardial Infarction (MI), Acute Kidney Injury(AKI), and Cerebrovascular Events (CVO)s.
| at postoperative first, sixth, twelfth and twenty-forth hours |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |