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Tailored Antibiotics Prophylaxis for Percutaneous Endoscopic Gastrostomy (PEG)

N

National Cheng Kung University

Status

Unknown

Conditions

The Patients Who Receive Percutaneous Endoscopic Gastrostomy
Peristomal Wound Infection After the Operation of PEG
Prophylactic Antibiotics Before PEG

Treatments

Drug: cefuroxime
Drug: Tailored antibiotic

Study type

Interventional

Funder types

Other

Identifiers

NCT01237730
NCKU-HR99

Details and patient eligibility

About

Tailored antibiotic prophylaxis according to the individual throat swab culture could reduce the peristomal infection rate

Full description

Past know-how:

Antibiotic prophylaxis has been shown to be effective to reduce peristomal infection.[9-11] The penicillin-or cephalosporin-based antibiotic prophylaxis are usually used with similar efficacy.[12] EuropeanSociety of Gastrointestinal Endoscopy (ESGE) guideline recommend that a single dose of intravenous cephalosporin orpenicillin as preparation before PEG.[17] The updated practice guidelines of American Society for Gastrointestinal Endoscopy (ASGE) and British Society of Gastroenterology (BSG) also recommend cefazolin or cefuroxime as prophylactic antibiotics.[18-19]

Question:

Is the 1st or 2nd generation cephalosporin is adequate as prophylactic antibiotics for percutaneous endoscopic gastrostomy (PEG)?

Preliminary results:

  1. The leading two common pathogen to cause peristomal infection of PEG are P. aeuroginosa and methecillin-resistanced S. aurous. (Figure 1) These two common pathogen can't be covered by the prophylactic antibiotics which suggested by guideline.
  2. The patient with airway infection before PEG had higher peristomal infection rate, comparing with those without airway infection. Moreover, adequate antibiotics prophylaxis could significant improve the infection rate. (Table 1)

Hypothesis:

Tailored antibiotic prophylaxis according to the individual throat swab culture could reduce the peristomal infection rate.

Specific aims:

  1. If individual tailored antibiotic prophylaxis according to throat swab could reduce the peristomal infection rate?
  2. If the phenotype and genotype analysis were compatible between infected wound isolates and throat swab/sputum isolates?
  3. If throat swab culture is better than sputum culture to predict peristomal infected microorganism?
  4. Is the infection is also linked to the oropharyngeal isolates if the patients get peristomal infection more than one week after PEG?

Anticipated results:

  1. Individual tailored antibiotic prophylaxis according to the throat swab culture could reduce the peristomal infection rate of PEG and short the days of hospitalization.
  2. Most phenotype and genotype are compatible between peristomal isolates and throat swab/sputum isolates. It indicates that most pathogens are carried from throat into the peristomal to cause the infection. The microorganism isolated from throat swab could predict the pathogen of PEG peristomal infection.
  3. The throat swab culture may be better than sputum culture to predict the peristomal infected pathogen because some unconscious patients is difficult to collect sputum.
  4. Peristomal infection more than one week after PEG may be not associated to throat pathogen. It may be related to the contamination during wound care.

Significances:

This proposal result could be applied to clinical care of percutaneous endoscopic gastrostomy. The individual chose of prophylactic antibiotics could improve the peristomal infection rate. Currently, 1st or 2nd cephalosporin was usually recommended as prophylaxis before PEG. However, for the patient with ORSA culture from nasal cavity, vancomycin was suggested as prophylaxis because some studies support the benefit on infection prevention. If the results are positive, it may change the clinical guideline on antibiotics prophylaxis before PEG.

Enrollment

100 estimated patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patients who receive PEG by pull method in our hospital, a tertiary transferring center, will be included

Exclusion criteria

  • The exclusion criteria for entry are inability to place the gastrostomy for technical reasons, such as oropharyngeal deformity or esophageal stricture. The patients who receive PEG by percutaneous push method will be excluded. The patients will be also excluded if active infection and fever are identified, and the PEG is delayed until the infection is brought under control.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Cefuroxime group
Active Comparator group
Description:
Use the cefuroxime as prophylactic antiobiotics, according to the clinical guideline.
Treatment:
Drug: cefuroxime
Tailored antibiotics group
Experimental group
Description:
Tailored antibiotic is selected according to the patient's oropharyngeal microorganisms.
Treatment:
Drug: Tailored antibiotic

Trial contacts and locations

1

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Central trial contact

chiao-hsiung chuang, M.D.

Data sourced from clinicaltrials.gov

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