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Empirical vs 2nd Line Antibiotic Therapy in Health-care Associated Infections in Cirrhosis

Primary Purpose

Cirrhosis

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Imipenem
Vancomycin
azithromycin
Cefotaxime
Amoxicillin
Sponsored by
University of Roma La Sapienza
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis focused on measuring healthcare infection cirrhosis antibiotic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • cirrhosis
  • healthcare infection
  • older than 18 years
  • agreement to participate

Exclusion Criteria:

  • HIV
  • patients underwent to liver transplantation

Sites / Locations

  • Manuela MerliRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Imipenem & Vancomycin & Azithromycin

Cefotaxime & Amoxicillin & Azithromycin

Arm Description

Tienam combined with vancomycin (1g/12 h) for Spontaneous bacterial peritonitis, cholangitis, sepsis without evidence of a source of infections. Tienam combined with vancomycin (1g/12 h)and azythromycin (500 mg/24 h)for pneumonia

Cefotaxime IV(2g/12 h): for Spontaneous bacterial peritonitis, cholangitis, sepsis without evidence of specific site of infection Amoxicillin/clavulanic acid (2,2 g/8 h)or Ciprofloxacin (500 mg/12 h: urinary tract infections Amoxicillin/clavulanic acid (2,2 g/8 h)and azithromycin (500 mg/24 h): pneumonia Amoxicillin/clavulanic acid (2,2 g/8 h)for skin or soft tissue infection

Outcomes

Primary Outcome Measures

Efficacy of anti-multiresistant empirical antibiotic therapy in healthcare associated infections in cirrhosis

Secondary Outcome Measures

Full Information

First Posted
October 16, 2012
Last Updated
May 28, 2015
Sponsor
University of Roma La Sapienza
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1. Study Identification

Unique Protocol Identification Number
NCT01820026
Brief Title
Empirical vs 2nd Line Antibiotic Therapy in Health-care Associated Infections in Cirrhosis
Official Title
Bacterial Infections Associated With Healthcare (Healthcare-Associated) in Hospitalized Cirrhotic Patients: Randomized Study of Use of Traditional Empirical Antibiotic Therapy and Second-line Targeted at Multi-resistant Bacteria
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Unknown status
Study Start Date
December 2012 (undefined)
Primary Completion Date
May 2015 (Actual)
Study Completion Date
June 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Roma La Sapienza

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Bacterial infections are a frequent complication in liver cirrhosis with a bad prognosis. However, the clinical outcome of cirrhotic patients with serious infections is significantly improved over the last 30 years due to early diagnosis and to the use of a more appropriate antibiotic therapy. As in the general population, empirical treatment should be initiated soon after diagnosis, after making the necessary sampling and should be based on the use of an antibiotic with low toxicity and broad spectrum antibacterial efficacy, taking into account the local epidemiology and prevalence of antibiotic resistance. The third generation cephalosporins are considered the gold standard in the treatment of most infections in cirrhotics due to their effectiveness against enterobacteriaceae and against non-enterococcal streptococci and due to their low toxicity. However, the recommendations for the antibiotic therapy are currently based on results of trials of '80s and '90s, when the proportion of resistant pathogens was lower. Similarly to nosocomial infections, the increasing rate of infections due to multidrug resistant (MDR) bacteria represents the rational for a different choice of empirical antibiotic therapy with a higher resistance barrier. This change in the epidemiology of community acquired infections is mainly due to the increased contacts with healthcare system of these patients and for the larger use of antibiotic prophylaxis. With this regard, it was recently proposed to introduce a third epidemiological class of infection "Health care-associated": Infections occurring in community in patients who have been in contact with the health system shortly before the infection. This epidemiological class of infection should be distinguished from "community-acquired" because they are more similar to"nosocomial" in terms of their sensitivity to antibiotics. Therefore for this class should be taken into consideration the use of a different empirical antibiotic therapy. The investigators aim was to evaluate prospectively the effectiveness of a broad spectrum antibiotic treatment in a cohort of cirrhotic patients with "healthcare-Associated"infections Cirrhotic patients with "Healthcare Associated" admitted to the gastroenterology department of the Policlinico Umberto I and in the Department of Hepatology of the Hospital of Marino will be consecutively enrolled. Randomized controlled trial with randomisation stratified by epidemiological class of infection.
Detailed Description
Unblinded randomized controlled trial with randomisation stratified by epidemiological class of infection. After obtaining informed consent at enrollment, participants will undergo medical examination with a detailed anamnesis and will begin collecting data on the following parameters: Demographic characteristics (age, sex, etiology of cirrhosis, when the diagnosis was made). Severity of liver disease(defined by the Child-Pugh classification, MELD score), indices of renal function and serum electrolytes. APACHE score in the case of development of sepsis Compensated cirrhosis / decompensated cirrhosis If decompensated, will be listed complications (ascites, esophageal-gastric varices, hepatic encephalopathy, coagulopathy, Hepato-Renal Syndrome, variceal bleeding). Treatment and dosage (eg β-blockers, diuretics) Hemodynamic parameters (heart rate / blood pressure) Patients enrolled will be randomized and treated with conventional therapy provided for community-acquired infections or with the "2nd line antibiotic therapy", based on use of of imipenem-cilastatin. The protocol of antibiotic therapy chosen for this category of patients will be based on a antibiotic class recommended for a specific site of infection in international guidelines for the treatment of nosocomial infections and / or healthcare associated with a high safety profile and is already used in the investigators hospital. The cost of empirical treatment with imipenem / cilastatin is roughly comparable to that with the currently used first-line antibiotics for such infections, and frequently used drugs in the forefront of these patients are ineffective is therefore necessary to embark on a new antibiotic with higher costs also in terms of days of hospitalization. During the hospitalization will be recorded the type of infection, empirical therapy, its duration, side effects, isolated pathogens and their resistance, when available, the occurrence of complications related to infection and mortality. The efficacy of therapy will be assessed based on the resolution of infection attested by normalization of clinical , biochemical and microbiological parameters and the instrumental tools.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis
Keywords
healthcare infection cirrhosis antibiotic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
96 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Imipenem & Vancomycin & Azithromycin
Arm Type
Experimental
Arm Description
Tienam combined with vancomycin (1g/12 h) for Spontaneous bacterial peritonitis, cholangitis, sepsis without evidence of a source of infections. Tienam combined with vancomycin (1g/12 h)and azythromycin (500 mg/24 h)for pneumonia
Arm Title
Cefotaxime & Amoxicillin & Azithromycin
Arm Type
Active Comparator
Arm Description
Cefotaxime IV(2g/12 h): for Spontaneous bacterial peritonitis, cholangitis, sepsis without evidence of specific site of infection Amoxicillin/clavulanic acid (2,2 g/8 h)or Ciprofloxacin (500 mg/12 h: urinary tract infections Amoxicillin/clavulanic acid (2,2 g/8 h)and azithromycin (500 mg/24 h): pneumonia Amoxicillin/clavulanic acid (2,2 g/8 h)for skin or soft tissue infection
Intervention Type
Drug
Intervention Name(s)
Imipenem
Other Intervention Name(s)
Tienam
Intervention Description
second line therapy
Intervention Type
Drug
Intervention Name(s)
Vancomycin
Other Intervention Name(s)
Vancocyn
Intervention Description
Second line therapy
Intervention Type
Drug
Intervention Name(s)
azithromycin
Other Intervention Name(s)
Zithromax
Intervention Description
Second line therapy
Intervention Type
Drug
Intervention Name(s)
Cefotaxime
Intervention Description
Standard antibiotic therapy
Intervention Type
Drug
Intervention Name(s)
Amoxicillin
Other Intervention Name(s)
Augmentin
Intervention Description
Standard therapy
Primary Outcome Measure Information:
Title
Efficacy of anti-multiresistant empirical antibiotic therapy in healthcare associated infections in cirrhosis
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: cirrhosis healthcare infection older than 18 years agreement to participate Exclusion Criteria: HIV patients underwent to liver transplantation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Manuela Merli, Prof
Phone
00390649972001
Email
clucidi@hotmail.it
First Name & Middle Initial & Last Name or Official Title & Degree
Cristina Lucidi, Dr
Phone
00393395263376
Email
clucidi@hotmail.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Manuela Merli, Prof
Organizational Affiliation
Gastroenterology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claudio Puoti, Prof
Organizational Affiliation
Department of Medicine Epatologica Marino Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Manuela Merli
City
Rome
ZIP/Postal Code
00100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Manuela Merli, Prof
Phone
00300649972001
Email
clucidi@hotmail.it
First Name & Middle Initial & Last Name & Degree
Cristina Lucidi, Dr
Phone
00393395263376
Email
clucidi@hotmail.it
First Name & Middle Initial & Last Name & Degree
Manuela Merli, Prof

12. IPD Sharing Statement

Citations:
PubMed Identifier
26529126
Citation
Merli M, Lucidi C, Di Gregorio V, Lattanzi B, Giannelli V, Giusto M, Farcomeni A, Ceccarelli G, Falcone M, Riggio O, Venditti M. An empirical broad spectrum antibiotic therapy in health-care-associated infections improves survival in patients with cirrhosis: A randomized trial. Hepatology. 2016 May;63(5):1632-9. doi: 10.1002/hep.28332. Epub 2016 Jan 5.
Results Reference
derived

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Empirical vs 2nd Line Antibiotic Therapy in Health-care Associated Infections in Cirrhosis

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