Abstract:EUS-FNA has a management impact in almost 72% of IPCs, with a major influence on the management strategy, either discharge rather than surgical resection or surgery rather than additional follow up.
“…In 11 studies, multi‐needle passes were reported; the post‐EUS‐FNA morbidity in these studies (2.17%, 95% CI: 1.21–3.40%) was similar to that in the nine studies which reported single‐needle pass (3.45%, 95% CI: 1.41–6.33%). The other 20 studies had no detailed information on the number of needle passes for EUS‐FNA.…”
Section: Resultssupporting
confidence: 55%
“…Of the 40 studies included, 11 studies with a total of 2127 patients were multicenter studies . The post‐EUS‐FNA adverse event morbidity in these studies (2.74%, 95% CI: 1.54–4.26%) was comparable to that in the 29 single‐center studies (2.63%, 95% CI: 1.58–3.95%).…”
Section: Resultsmentioning
confidence: 87%
“…An analysis of the potential risk factors for adverse events after EUS‐FNA is presented in Table . Pooled data from 19 prospective studies showed a post‐EUS‐FNA adverse event morbidity of 3.69% (95% CI: 2.22–5.54%), whereas in the 21 retrospective studies the post‐EUS‐FNA incidence of adverse events was 1.90% (95% CI: 1.05–2.98%). There was no significant difference between prospective and retrospective studies in this respect.…”
Section: Resultsmentioning
confidence: 96%
“…A total of 40 articles with a combined study population of 5124 patients who underwent EUS‐FNA of PCL were included in this analysis. Of these 40 articles, 19 were prospective studies, and 11 were multicenter studies (Fig ; Table ).…”
Section: Resultsmentioning
confidence: 99%
“…One study found no association of needle size with the risk of post‐EUS‐FNA adverse events. Previous studies have shown that needle malfunction was similar between the 22 G needle and the 25 G needle in solid pancreatic lesions .…”
EUS-FNA is a safe procedure for diagnosis of PCL and is associated with a relatively low incidence of adverse events. Most adverse events were mild, self-limiting, and did not require medical intervention.
“…In 11 studies, multi‐needle passes were reported; the post‐EUS‐FNA morbidity in these studies (2.17%, 95% CI: 1.21–3.40%) was similar to that in the nine studies which reported single‐needle pass (3.45%, 95% CI: 1.41–6.33%). The other 20 studies had no detailed information on the number of needle passes for EUS‐FNA.…”
Section: Resultssupporting
confidence: 55%
“…Of the 40 studies included, 11 studies with a total of 2127 patients were multicenter studies . The post‐EUS‐FNA adverse event morbidity in these studies (2.74%, 95% CI: 1.54–4.26%) was comparable to that in the 29 single‐center studies (2.63%, 95% CI: 1.58–3.95%).…”
Section: Resultsmentioning
confidence: 87%
“…An analysis of the potential risk factors for adverse events after EUS‐FNA is presented in Table . Pooled data from 19 prospective studies showed a post‐EUS‐FNA adverse event morbidity of 3.69% (95% CI: 2.22–5.54%), whereas in the 21 retrospective studies the post‐EUS‐FNA incidence of adverse events was 1.90% (95% CI: 1.05–2.98%). There was no significant difference between prospective and retrospective studies in this respect.…”
Section: Resultsmentioning
confidence: 96%
“…A total of 40 articles with a combined study population of 5124 patients who underwent EUS‐FNA of PCL were included in this analysis. Of these 40 articles, 19 were prospective studies, and 11 were multicenter studies (Fig ; Table ).…”
Section: Resultsmentioning
confidence: 99%
“…One study found no association of needle size with the risk of post‐EUS‐FNA adverse events. Previous studies have shown that needle malfunction was similar between the 22 G needle and the 25 G needle in solid pancreatic lesions .…”
EUS-FNA is a safe procedure for diagnosis of PCL and is associated with a relatively low incidence of adverse events. Most adverse events were mild, self-limiting, and did not require medical intervention.
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