The Use of Prophylactic Somatostatin Therapy Following Pancreaticoduodenectomy: A Meta-analysis of Randomised Controlled Trials
Background Prophylactic administration of somatostatin analogues (SA) to reduce the incidence of post-operative pancreatic fistula (POPF) remains contentious. This meta-analysis evaluated its impact on outcomes following pancreaticoduodenectomy (PD). Methods The EMBASE, MEDLINE and Cochrane database...
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Veröffentlicht in: | World journal of surgery 2019-07, Vol.43 (7), p.1788-1801 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
Prophylactic administration of somatostatin analogues (SA) to reduce the incidence of post-operative pancreatic fistula (POPF) remains contentious. This meta-analysis evaluated its impact on outcomes following pancreaticoduodenectomy (PD).
Methods
The EMBASE, MEDLINE and Cochrane databases were searched for randomised controlled trials (RCTs) investigating prophylactic SA following PD. Comparative effects were summarised as odds ratio and weighted mean difference based on an intention to treat. Quantitative pooling of the effect sizes was derived using the random-effects model.
Main results
Twelve RCTs were included involving 1615 patients [SA-treated group (
n
= 820) and control group (
n
= 795)]. The SA used included somatostatin-14, pasireotide, vapreotide and octreotide. Pooling of the data showed no significant benefit of its use for the primary outcome measure of all grades of POPF, odds ratio (OR) 0.73 [95% confidence interval (CI), 0.51–1.05,
p
= 0.09] and clinically relevant POPF, OR 0.48 [95% CI, 0.22–1.06,
p
= 0.07]. There were no benefits in the secondary outcome measures of delayed gastric emptying, OR 0.98 [95% CI, 0.57–1.69,
p
= 0.94]; infected abdominal collections, OR 0.80 [95% CI, 0.44–1.43,
p
= 0.80]; reoperation rates, OR 1.24 [95% CI, 0.73–2.13,
p
= 0.42]; duration of hospital stay, − 0.23 [95% CI − .59 to 1.13,
p
= 0.74]; and mortality, 1.78 [95% CI, 0.94–3.39,
p
= 0.08].
Conclusion
SA did not improve the post-operative outcomes following PD, including reducing the incidence of POPF. The routine administration of SA cannot be recommended following PD. |
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ISSN: | 0364-2313 1432-2323 |
DOI: | 10.1007/s00268-019-04956-6 |