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Spinal Versus General Anesthesia for Laparoscopic Cholecystectomy

Μόνο εγγεγραμμένοι χρήστες μπορούν να μεταφράσουν άρθρα
Σύνδεση εγγραφή
Ο σύνδεσμος αποθηκεύεται στο πρόχειρο
ΚατάστασηΟλοκληρώθηκε το
Χορηγοί
Medical Park Gaziantep Hospital
Συνεργάτες
Zeugma Saglik Hizmetleri San. Tic. Ltd. Sti.

Λέξεις-κλειδιά

Αφηρημένη

The aim of this study is to compare early postoperative outcomes of unselected consecutive patients underwent laparoscopic cholecystectomy (LC) under spinal versus general anesthesia.

Περιγραφή

Laparoscopic cholecystectomy (LC) is the gold standard surgical treatment of symptomatic cholecystectomy which traditionally performed under general anesthesia. Laparoscopy has provided many advantages over open surgery for the patients; however, general anesthesia adversely affects patients' early postoperative quality of life (POQoL).

Spinal anesthesia which is a less invasive technique compared to general anesthesia has many advantages regarding the POQoL such as no need to wait for recovery from anesthesia, less nausea and vomiting, less or no pain at the end of surgery, no discomfort associated with intubation, early ambulation, fully awaken and oriented patient in the bed, and less anxious relatives.

LC has been shown to be feasible under spinal anesthesia if performed with proper technique. There are many reports demonstrated the effectiveness and safety of LC under spinal anesthesia in selected patients. However, patients with complicated gallstone disease such as acute, gangrenous or subacute cholecystitis have been considered as unfit cases for LC under spinal anesthesia because of technical difficulties. On the other hand, spinal anesthesia has also been regarded as inappropriate for patients complying with American society for anesthesiology (ASA) III and IV due to the uncontrolled anesthesia risks.

The aim of this study is to compare early postoperative outcomes of unselected consecutive patients underwent LC under spinal versus general anesthesia. If proportion of general anesthesia (PGA) / proportion of spinal anesthesia (PSA) denotes the proportion rate of outcomes in the general anesthesia group (GaG) / spinal anesthesia group (SaG), then two-sided test problem is assessed as follow:

1. Null hypothesis: H0: PGA = PSA. There is no difference between the two anesthesia techniques in terms of primary outcomes.

2. Null hypothesis: H1: PGA ≠ PSA There is a difference between the two anesthesia techniques in terms of primary outcomes.

Ημερομηνίες

Τελευταία επαλήθευση: 10/31/2016
Πρώτα υποβλήθηκε: 10/29/2016
Υποβλήθηκε εκτιμώμενη εγγραφή: 11/03/2016
Δημοσιεύτηκε για πρώτη φορά: 11/06/2016
Υποβλήθηκε τελευταία ενημέρωση: 11/03/2016
Δημοσιεύτηκε η τελευταία ενημέρωση: 11/06/2016
Ημερομηνία έναρξης της πραγματικής μελέτης: 05/31/2008
Εκτιμώμενη κύρια ημερομηνία ολοκλήρωσης: 05/31/2016
Εκτιμώμενη ημερομηνία ολοκλήρωσης μελέτης: 07/31/2016

Κατάσταση ή ασθένεια

Cholecystitis
Gallbladder Diseases

Παρέμβαση / θεραπεία

Procedure: Spinal anesthesia group

Procedure: General anesthesia

Φάση

-

Ομάδες βραχιόνων

ΜπράτσοΠαρέμβαση / θεραπεία
Spinal anesthesia group
patients underwent laparoscopic cholecystectomy under spinal anesthesia
Procedure: Spinal anesthesia group
Spinal anesthesia was used in patients who underwent LC
General anesthesia
Patients underwent laparoscopic cholecystectomy under general anesthesia
Procedure: General anesthesia
General anesthesia was used in patients who underwent LC

Κριτήρια καταλληλότητας

Φύλα επιλέξιμα για μελέτηAll
Μέθοδος δειγματοληψίαςProbability Sample
Δέχεται υγιείς εθελοντέςΝαί
Κριτήρια

Inclusion Criteria:

- All patients who underwent laparoscopic cholecystectomy for symptomatic gallstone disease with no restriction for age, gender, ethnicity, disease severity, and ASA grade.

Exclusion Criteria:

- Patients were excluded if they underwent concurrent surgeries, had malignancy suspicion, received or converted to open surgery, and patients who were under spinal anesthesia converted to general anesthesia.

Αποτέλεσμα

Πρωτεύοντα αποτελέσματα

1. Change in pain level for the first day [from baseline to postoperative 1, 2, 4 and 6 hours]

Numerical rating scale (NRS) was used

2. Change in pain level for the first month [From postoperative 1 week to 1 month]

Numerical rating scale was used

Δευτερεύοντα αποτελέσματα

1. Complications [within the postoperative 1 month]

All types of complications were assessed

2. Mortality [within the postoperative 1 month]

all causes of mortality were recorded

3. Gastrointestinal quality of life index [change from baseline to postoperative 1 week and 1 month]

A standard form was used under the supervision of experienced independent personal

4. Patient satisfaction [at postoperative 1 month]

a verbal or visual scale was used

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