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Effects of Chengqi Decoction on Complications and Prognosis of Patients with Pneumonia-Derived Sepsis: Retrospective Cohort Study
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Purpose. A specific and efficacious method for treatment of pneumonia-derived sepsis is lacking. Chengqi decoction has been used for treatment of pneumonia-derived sepsis, but a clinical trial on patients with pneumonia-derived sepsis is lacking, a gap in the literature that we sought to fill. Patients and Methods. 282 patients with pneumonia-derived sepsis admitted to the intensive care unit of our hospital were selected. They were divided into the treatment group (141 cases) and control group (141 cases). Both groups underwent conventional treatment, but Chengqi decoction (in the form of enema) was given to the treatment group. Mortality, morbidity (abdominal distension and gastrointestinal bleeding), duration of antibiotic use, and use of vasoactive agents were documented 28 days after the drug was used. Results. The treatment group reduced mortality and morbidity (abdominal distension) (
P
<
0.05
). After adjustment for significant covariates, 28-day survival was similar for the whole group (hazard ratio (HR): 0.48; 95% confidence interval (CI): 0.23–0.97;
P
=
0.037
), for the subgroup (n = 120) with Acute Physiology and Chronic Health Evaluation II score ≥25 (HR: 0.180; 95% CI: 0.032–0.332;
P
=
0.039
) and for the subgroup (n = 66) with N-terminal B-type natriuretic peptide <1800 (0.059, 0.004–0.979, and 0.019). There was no difference between the two groups for the duration of antibiotic use, major bleeding, or use of vasoactive drugs. Conclusions. Chengqi decoction improved 28-day survival and reduced the prevalence of abdominal distension in patients with pneumonia-derived sepsis.
Title: Effects of Chengqi Decoction on Complications and Prognosis of Patients with Pneumonia-Derived Sepsis: Retrospective Cohort Study
Description:
Purpose.
A specific and efficacious method for treatment of pneumonia-derived sepsis is lacking.
Chengqi decoction has been used for treatment of pneumonia-derived sepsis, but a clinical trial on patients with pneumonia-derived sepsis is lacking, a gap in the literature that we sought to fill.
Patients and Methods.
282 patients with pneumonia-derived sepsis admitted to the intensive care unit of our hospital were selected.
They were divided into the treatment group (141 cases) and control group (141 cases).
Both groups underwent conventional treatment, but Chengqi decoction (in the form of enema) was given to the treatment group.
Mortality, morbidity (abdominal distension and gastrointestinal bleeding), duration of antibiotic use, and use of vasoactive agents were documented 28 days after the drug was used.
Results.
The treatment group reduced mortality and morbidity (abdominal distension) (
P
<
0.
05
).
After adjustment for significant covariates, 28-day survival was similar for the whole group (hazard ratio (HR): 0.
48; 95% confidence interval (CI): 0.
23–0.
97;
P
=
0.
037
), for the subgroup (n = 120) with Acute Physiology and Chronic Health Evaluation II score ≥25 (HR: 0.
180; 95% CI: 0.
032–0.
332;
P
=
0.
039
) and for the subgroup (n = 66) with N-terminal B-type natriuretic peptide <1800 (0.
059, 0.
004–0.
979, and 0.
019).
There was no difference between the two groups for the duration of antibiotic use, major bleeding, or use of vasoactive drugs.
Conclusions.
Chengqi decoction improved 28-day survival and reduced the prevalence of abdominal distension in patients with pneumonia-derived sepsis.
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