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Long-term outcomes of direct percutaneous endoscopic jejunostomy: a 10-year cohort.

Direct percutaneous endoscopic jejunostomy patients assessed over 10 years for clinical outcomes.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12614001138673
Enrollment
83
Registered
2014-10-27
Start date
2003-08-12
Completion date
2013-10-24
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

To assess clinical outcomes of patients who received direct percutaneous endoscopic jejunostomy (DPEJ) for enteral feeding.

Interventions

All direct percutaneous endoscopic jejunostomy (DPEJs) were performed by two experienced interventional endoscopists (MS and NN), using a paediatric colonoscope (Olympus, GHG180) and a standard Ponsky PEG kit. All subjects received prophylactic antibiotic 1 hour prior to the procedure (Cephazolin 1gm IV; or Vancomycin 1gm IV if known to have penicillin allergy). The scope was advanced into the jejunum as far as possible. With the room light dimmed, the abdomen was closely observed for the light

All direct percutaneous endoscopic jejunostomy (DPEJs) were performed by two experienced interventional endoscopists (MS and NN), using a paediatric colonoscope (Olympus, GHG180) and a standard Ponsky PEG kit. All subjects received prophylactic antibiotic 1 hour prior to the procedure (Cephazolin 1gm IV; or Vancomycin 1gm IV if known to have penicillin allergy). The scope was advanced into the jejunum as far as possible. With the room light dimmed, the abdomen was closely observed for the light trans-lumination from the scope tip as the scope slowly withdrew. Once good light trans-lumination was identified, the overlying skin was quickly cleansed with local anti-septic and a 22G needle was used to puncture into the lumen of the jejunal loop under direct endoscopic vision. This is to temporarily fix and secure the relevant jejunal loop to the abdomen wall, allowing time for injection of local anaesthesia (lignocaine 2%, 10ml), insertion of a larger bore trocar needle and a small skin incision. A plastic loop-wire was then feed through the trocar needle, which was grasped by a snare and pulled out of the mouth by removing the scope. The PEG tube was attached to the loop-wire, pulled through the mouth into the jejunum and out the abdominal wall at the DPEJ site. The inner bumper was retracted against the anterior abdominal wall and fixed by a plastic disc. The procedure lasts for up to an hour. The overall duration of observation for each patient was up to 10 years.

Sponsors

Nam Q Nguyen
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients who were referred for DJEP insertion between 2003 and 2013 at the Gastrointestinal Investigation Unit of the Royal Adelaide Hospital

Exclusion criteria

Exclusion criteria for DPEJ placement included ascites, peritonitis, peritoneal carcinosis, coagulation disorders (prothrombin time of less than 50%; thrombocytes less than 50x109/L) and inability to give consent.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026