OBJECTIVE:Morbidity and mortality following perforated peptic ulcer (PPU) remain substantial. In the recently published PULP trial, 30-day mortality in patients surgically treated for PPU decreased from 27% to 17% following the implementation of a perioperative care protocol based on The Surviving Sepsis Guidelines. The objective of the present study was to evaluate long-term mortality in the PULP trial intervention and control cohort. DESIGN: nationwide follow-up study of a multicenter, non-randomized, clinical trial with external controls. SETTING:Danish patients surgically treated for PPU between 1 January 2008 and 31 December 2009. PATIENTS: 117 patients in the intervention group and 512 in the control group. INTERVENTION: a perioperative care protocol based on The Surviving Sepsis Guidelines. OUTCOME MEASURES: 60-day, 90-day, 180-day, 1-year, and 2-year mortality rates. STATISTICAL ANALYSIS: survival statistics. RESULTS: Baseline characteristics, clinical, and perioperative data were in general, similar in the intervention and control group. Sixty days postoperatively, the originally observed difference in 30-day mortality had diminished (25% vs. 30%, p = 0.268). After 180 days, the mortality difference was reduced additionally (31% vs. 33%, p = 0.645), and one year postoperatively, a mortality difference was no longer present (36% in both groups, p = 0.993). Two years postoperatively, the mortality rate in the intervention group was 44%, as compared to 40% in the control group (p = 0.472). CONCLUSIONS: The survival benefit associated with a perioperative care protocol in patients treated for PPU decreases progressively after 30 days and is no longer present after one year. REGISTRATION NUMBER: NCT00624169 ( http://www.clinicaltrials.gov ).
RCT Entities:
OBJECTIVE: Morbidity and mortality following perforated peptic ulcer (PPU) remain substantial. In the recently published PULP trial, 30-day mortality in patients surgically treated for PPU decreased from 27% to 17% following the implementation of a perioperative care protocol based on The Surviving Sepsis Guidelines. The objective of the present study was to evaluate long-term mortality in the PULP trial intervention and control cohort. DESIGN: nationwide follow-up study of a multicenter, non-randomized, clinical trial with external controls. SETTING: Danish patients surgically treated for PPU between 1 January 2008 and 31 December 2009. PATIENTS: 117 patients in the intervention group and 512 in the control group. INTERVENTION: a perioperative care protocol based on The Surviving Sepsis Guidelines. OUTCOME MEASURES: 60-day, 90-day, 180-day, 1-year, and 2-year mortality rates. STATISTICAL ANALYSIS: survival statistics. RESULTS: Baseline characteristics, clinical, and perioperative data were in general, similar in the intervention and control group. Sixty days postoperatively, the originally observed difference in 30-day mortality had diminished (25% vs. 30%, p = 0.268). After 180 days, the mortality difference was reduced additionally (31% vs. 33%, p = 0.645), and one year postoperatively, a mortality difference was no longer present (36% in both groups, p = 0.993). Two years postoperatively, the mortality rate in the intervention group was 44%, as compared to 40% in the control group (p = 0.472). CONCLUSIONS: The survival benefit associated with a perioperative care protocol in patients treated for PPU decreases progressively after 30 days and is no longer present after one year. REGISTRATION NUMBER: NCT00624169 ( http://www.clinicaltrials.gov ).
Authors: Kjetil Søreide; Kenneth Thorsen; Ewen M Harrison; Juliane Bingener; Morten H Møller; Michael Ohene-Yeboah; Jon Arne Søreide Journal: Lancet Date: 2015-09-26 Impact factor: 79.321