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1 ed toxicity (five thromboembolic events, one bowel perforation).
2         Two patients had a delayed diagnosed bowel perforation.
3 lar access thrombosis (2%), stroke (2%), and bowel perforation (1%).
4 ed deaths (disseminated disease, 4 patients; bowel perforation, 1 patient).
5  with inadequate distribution (7%) and small-bowel perforation (3%) make the otherwise less toxic 32P
6  despite the PKD group's higher incidence of bowel perforation and increased age at time of transplan
7 ocedures (hepatic arterial hemorrhage, small bowel perforation, and liver decompensation salvaged by
8 onal age, ductus closure, occurrence of NEC, bowel perforation, and mortality.
9 atment were gastrointestinal bleeding, small-bowel perforation, and the development of enterocolic fi
10 A on colonoscopy complications, specifically bowel perforation, aspiration pneumonia, and splenic inj
11 %) in emergency neonatal surgeries involving bowel perforation, bowel resection, congenital diaphragm
12                                              Bowel perforation can lead to significant bacterial spil
13                      The primary outcome was bowel perforation, defined using a validated algorithm.
14                                Delayed small bowel perforation following BAT is thought to occur seco
15 is is the first case report of delayed small bowel perforation following BAT with extensive portomese
16 re of any other case report of delayed small bowel perforation following BAT without signs of intraab
17                               Isolated small bowel perforation following blunt abdominal trauma (BAT)
18 cate that there is increased risk of NEC and bowel perforation in premature infants with PDA receivin
19 ctivated FXII (FXIIa) modifies the course of bowel perforation-induced peritoneal sepsis in mice.
20 idity and mortality rates, and delayed small bowel perforation is even rarer.
21 reased risk of aspiration pneumonia, but not bowel perforation or splenic injury.
22                                           No bowel perforations or fistulas occurred.
23          Progression-free survival (PFS) and bowel perforation rates were taken from recently reporte
24 cept for acute medical conditions, including bowel perforation (relative risk [RR] = 3.0, 95% confide
25                         Vascular thromboses, bowel perforation, septicemia, and retransplantation, ea
26   Treatment with 14E11 within 12 hours after bowel perforation significantly improved survival compar
27 ications (bleeding, transfusion requirement, bowel perforation, surgical intervention, and graft loss
28 GOG 218 at the baseline estimates of PFS and bowel perforation, the cost of PC was $2.5 million, comp
29                                              Bowel perforation was noted in 27 cases (30%).
30 events such as hypertension, thrombosis, and bowel perforation were also observed at rates consistent
31 was seen with the 7-day infusions (including bowel perforation), with 600,000 IU/m2 as the maximum-to

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