Acute Appendicitis. Acute Appendicitis
Conditions
Interventions
Intervention 1: 1)The first intervention group patients after surgery in the supine position and will receive three doses of antibiotics as directed by physician and 2 Hours, 2 and 24 hours after surg
Prevention
1)The first intervention group patients after surgery in the supine position and will receive three doses of antibiotics as directed by physician and 2 Hours, 2 and 24 hours after surgery for inflamma
2)In the second intervention group patients after surgery in the supine position and will receive one dose of antibiotics as directed by their physician and 2 Hours, 2 and 24 hours after surgery for i
3)In the third study, patients received three doses of antibiotics after surgery, according to the doctor and have a semi-upright position and 2 Hours, 2 and 24 hours after surgery for inflammatory ma
4)In the fourth study, patients after surgery with a dose of antibiotics will have a semi-upright position and 2 Hours, 2 and 24 hours after surgery for inflammatory markers CRP, ESR, leukocytes, neut
Sponsors
Vice chancellor for research, Dezful University of Medical Sciences
Eligibility
Sex/Gender
All
Age
10 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria : All patients on the basis of history and physical examination and laboratory findings; the diagnosis of acute appendicitis underwent appendectomy be; People aged 10 to 50 years; Not addicted to drugs; there is no underlying disease that is caused by elevated inflammatory markers before surgery; Consent to participate in the study and blood; having full consciousness baseline; If the body's inflammatory factors in sample 2 hours before and 2 hours after surgery are higher than normal. Exclusion Criteria : Diabetes; cancer; patients who had normal appendicitis; Patients with a history of previous infections and antibiotic use during the past week, a history of allergy to cephalosporins; Patients receiving immunosuppressive such as corticosteroids and cytotoxic drugs or taking anti-inflammatory drugs; Patients release from the hospital earlier than 24 hours.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CRP. Timepoint: 2 Hours Before; 2 And 24 Hours After Intervention (reposition). Method of measurement: Blood Samples, Immuno-agglutination Assay.;ESR. Timepoint: 2 Hours Before; 2 And 24 Hours After Intervention (reposition). Method of measurement: Blood Samples, Green Blot Method.;Leukocytes. Timepoint: 2 Hours Before; 2 And 24 Hours After Intervention (reposition). Method of measurement: Blood Samples, Cell Count Method.;Neutrophils. Timepoint: 2 Hours Before; 2 And 24 Hours After Intervention (reposition). Method of measurement: Blood Samples, Cell Count Method.;Temperature. Timepoint: 2 Hours Before; 2 And 24 Hours After Intervention (reposition). Method of measurement: Mercury Thermometer. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Maniey
Dezful University of Medical Sciences
Outcome results
None listed