1997
DOI: 10.1097/00006254-199704000-00012
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A Randomized Controlled Trial of Postoperative Nasogastric Tube Decompression in Gynecologic Oncology Patients Undergoing Intra-Abdominal Surgery

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Cited by 3 publications
(13 citation statements)
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“…One9 was a follow‐up report with a new outcome (ventral hernia) from a group of patients reported previously7. A broad range of abdominal surgery was covered in these papers; there were seven on colorectal surgery3, 7, 10–14, seven on gastroduodenal surgery2, 15–20, two each on biliary21, 22 and gynaecological23, 24 surgery, one each on vascular25 and emergency trauma26 surgery, and seven that included all facets of abdominal surgery1, 4, 6, 27–30. The included publications described 4195 participants, 2108 randomized to prophylactic nasogastric tube insertion for postoperative decompression, and 2087 randomized to no tube in the postoperative period.…”
Section: Resultsmentioning
confidence: 99%
“…One9 was a follow‐up report with a new outcome (ventral hernia) from a group of patients reported previously7. A broad range of abdominal surgery was covered in these papers; there were seven on colorectal surgery3, 7, 10–14, seven on gastroduodenal surgery2, 15–20, two each on biliary21, 22 and gynaecological23, 24 surgery, one each on vascular25 and emergency trauma26 surgery, and seven that included all facets of abdominal surgery1, 4, 6, 27–30. The included publications described 4195 participants, 2108 randomized to prophylactic nasogastric tube insertion for postoperative decompression, and 2087 randomized to no tube in the postoperative period.…”
Section: Resultsmentioning
confidence: 99%
“…1,19,[22][23][24][25][26][27][28][29] Randomization was based on a computerized randomization table only in 3 trials. [30][31][32] Therefore, concealment of allocation was ensured only in these 3 trials. The nature of the intervention made blinding impossible for patients and medical professionals.…”
Section: Trial Qualitymentioning
confidence: 99%
“…In the early-removal group, NGI was terminated at the end of the operation in 53% (9/17) of the trials. 3,4,20,23,[26][27][28][29]32 In 4 trials, 19,25,30,31 NGI was discontinued within 24 hours after surgery. In the remaining 4 trials, 1,21,22,24 patients received no NGI at all.…”
Section: Trial Characteristicsmentioning
confidence: 99%
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“…[3][4][5][6][7][8][9][10][11][12][13] Several series presented no differences between two groups found in terms of wound infection. 8,12 So wound dehiscence is not considered as parameter to compare between two groups in our study design. On the other hand Cheadle 6 reported 6 patients in Group I and 4 patients in Group II, while Bauer et al 3 had 3 patients in Group I and 2 patients in Group II.…”
Section: Discussionmentioning
confidence: 99%