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1.
Pharmacol Res ; 159: 104954, 2020 09.
Article in English | MEDLINE | ID: mdl-32492490

ABSTRACT

Fecal microbiota transplant (FMT) has seen a historic emergence in last decade with its sojourn recently entering into a chequered path, due to a few reports of infection and subsequent mortality. Though FMT has been extensively reported, there is no comprehensive report on the delivery routes available for this non-pharmacological treatment option. Safety, efficacy and cost of FMT not only depend on the quality of contents but also on the delivery route employed. A number of delivery routes are in use for conducting FMT, which include upper gastrointestinal routes (UGI) i.e. nasogastric/nasojejunal tube, endoscopy, oral capsules and lower gastrointestinal routes (LGI) like retention enema, sigmoidoscopy or colonoscopy. Capsules, both conventional as well as colon targeted have been the most commonly used formulations. Surprisingly, the success rates with conventional gastric delivery capsules and colon targeted capsules were found to be quite similar indicating the sufficiency of the inoculum size to withstand the microbial loss in the gastric milieu. Patient compliance, cost effectiveness, comfort of administration, level of invasiveness, patient's hospital admission, risk of aspiration and infections, multiplicity of administration required, recurrence rate are the main factors that seem to influence the choice for route of administration of physicians. The best route for FMT has not been established yet. Extensive studies are required to understand the interplay of route adopted, type of donor, physical nature of sample (fresh or frozen), patient compliance and cost effectiveness to design an approach for the risk free, convenient and cost-effective administration route for FMT.


Subject(s)
Cecostomy , Endoscopy, Digestive System , Fecal Microbiota Transplantation , Gastrointestinal Diseases/therapy , Gastrointestinal Microbiome , Animals , Capsules , Cecostomy/adverse effects , Cecostomy/instrumentation , Dysbiosis , Endoscopy, Digestive System/adverse effects , Endoscopy, Digestive System/instrumentation , Fecal Microbiota Transplantation/adverse effects , Fecal Microbiota Transplantation/instrumentation , Gastrointestinal Diseases/microbiology , Gastrointestinal Diseases/physiopathology , Humans , Treatment Outcome
2.
Curr Opin Pharmacol ; 49: 11-16, 2019 12.
Article in English | MEDLINE | ID: mdl-31059962

ABSTRACT

Fecal microbiota transplantation (FMT), the core therapy for remodeling the gut microbiota with a long medical history, has gained great attention worldwide in recent years. Increasing studies have explored its indications, methodology, efficacy, safety, and ethics. Purified forms of FMT, using an automated method for the purification of fecal microbiota from stool, has become a reality. Colonic transendoscopic enteral tubing makes frequent FMT delivery into the whole colon feasible. This review focuses on the recent progress in laboratory preparation, updated clinical strategies, novel delivery methods, and ethical issues surrounding FMT in clinical studies.


Subject(s)
Fecal Microbiota Transplantation , Donor Selection , Fecal Microbiota Transplantation/ethics , Fecal Microbiota Transplantation/instrumentation , Fecal Microbiota Transplantation/methods , Humans , Tissue Donors
3.
Clin. microbiol. infect ; 25(7): [1-11], Jan. 29, 2019.
Article in English | BIGG - GRADE guidelines | ID: biblio-1094956

ABSTRACT

The aim of these guidelines is to provide recommendations for decolonizing regimens targeting multidrug-resistant Gram-negative bacteria (MDR-GNB) carriers in all settings. Methods: These evidence-based guidelines were produced after a systematic review of published studies on decolonization interventions targeting the following MDR-GNB: third-generation cephalosporinresistant Enterobacteriaceae (3GCephRE), carbapenem-resistant Enterobacteriaceae (CRE), aminoglycoside-resistant Enterobacteriaceae (AGRE), fluoroquinolone-resistant Enterobacteriaceae (FQRE), extremely drug-resistant Pseudomonas aeruginosa (XDRPA), carbapenem-resistant Acinetobacter baumannii (CRAB), cotrimoxazole-resistant Stenotrophomonas maltophilia (CRSM), colistin-resistant Gram-negative organisms (CoRGNB), and pan-drug-resistant Gram-negative organisms (PDRGNB). The recommendations are grouped by MDR-GNB species. Faecal microbiota transplantation has been discussed separately. Four types of outcomes were evaluated for each target MDR-GNB:(a) microbiological outcomes (carriage and eradication rates) at treatment end and at specific post-treatment time-points; (b) clinical outcomes (attributable and all-cause mortality and infection incidence) at the same timepoints and length of hospital stay; (c) epidemiological outcomes (acquisition incidence, transmission and outbreaks); and (d) adverse events of decolonization (including resistance development). The level of evidence for and strength of each recommendation were defined according to the GRADE approach. Consensus of a multidisciplinary expert panel was reached through a nominal-group technique for the final list of recommendations.


Subject(s)
Cephalosporins/therapeutic use , Gram-Negative Bacterial Infections/diagnosis , Gram-Negative Bacterial Infections/prevention & control , Gram-Negative Bacterial Infections/transmission , Fluoroquinolones/therapeutic use , Enterobacteriaceae Infections/diagnosis , Enterobacteriaceae Infections/prevention & control , Enterobacteriaceae Infections/transmission , Aminoglycosides/therapeutic use , Cephalosporin Resistance/drug effects , Fecal Microbiota Transplantation/instrumentation , Evidence-Informed Policy
4.
Dig Dis Sci ; 64(6): 1672-1678, 2019 06.
Article in English | MEDLINE | ID: mdl-30519847

ABSTRACT

BACKGROUND: Fecal microbiota transplantation (FMT) is an effective therapy for recurrent Clostridium. difficile infection (rCDI). FMT capsules have emerged, and it is unknown if delivery location and dose impact efficacy. METHODS: We compared two cohorts of patients receiving two capsule formulations: gastric release (FMTgr) and targeted colonic release (FMTcr) at two different sites. Cohort A received FMTgr at (1) high dose: 60 capsules and low dose: 30 capsules. Patients in Cohort B received FMTcr at (1) high dose: 30 capsules (2) low dose: 10 capsules. Clinical cure rates and adverse events were monitored through week 8. Paired t-tests were used to compare diversity pre- and post-FMT. RESULTS: 51 rCDI patients were enrolled. Cohort A contained n = 20 and Cohort B contained n = 31. Overall cure at week 8 for FMTgr was 75% (15/20) compared to 80.6% for FMTcr, (25/31), p = 0.63. Both formulations were safe with no serious adverse events. FMTcr was superior at increasing gut microbial diversity. DISCUSSION: To our knowledge, this is the first study to compare targeted delivery of FMT capsules. While both capsules were safe and efficacious, microbial engraftment patterns were superior in FMTcr.


Subject(s)
Clostridium Infections/therapy , Colon/microbiology , Fecal Microbiota Transplantation/instrumentation , Gastrointestinal Microbiome , Stomach/microbiology , Adult , Aged , Aged, 80 and over , Capsules , Clostridium Infections/diagnosis , Clostridium Infections/microbiology , Fecal Microbiota Transplantation/adverse effects , Female , Humans , Hydrogen-Ion Concentration , Male , Middle Aged , Remission Induction , Time Factors , Treatment Outcome , Young Adult
6.
World J Gastroenterol ; 24(47): 5403-5414, 2018 Dec 21.
Article in English | MEDLINE | ID: mdl-30598584

ABSTRACT

AIM: To evaluate and describe the efficacy of fecal microbiota transplantation (FMT) for Clostridium difficile infection (CDI) in a national Israeli cohort. METHODS: All patients who received FMT for recurrent (recurrence within 8 wk of the previous treatment) or refractory CDI from 2013 through 2017 in all the five medical centers in Israel currently performing FMT were included. Stool donors were screened according to the Israeli Ministry of Health guidelines. Clinical and laboratory data of patients were collected from patients' medical files, and they included indications for FMT, risk factors for CDI and disease severity. Primary outcome was FMT success (at least 2 mo free of CDI-related diarrhea post-FMT). Secondary outcomes included initial response to FMT (cessation of diarrhea within 7 d) and recurrence at 6 mo. RESULTS: There were 111 FMTs for CDI, with a median age of 70 years [interquartile range (IQR): 53-82], and 42% (47) males. Fifty patients (45%) were treated via the lower gastrointestinal (LGI, represented only by colonoscopy) route, 37 (33%) via capsules, and 24 (22%) via the upper gastrointestinal (UGI) route. The overall success rate was 87.4% (97 patients), with no significant difference between routes of administration (P = 0.338). In the univariant analysis, FMT success correlated with milder disease (P = 0.01), ambulatory setting (P < 0.05) and lower Charlson comorbidity score (P < 0.05). In the multivariant analysis, only severe CDI [odd ratio (OR) = 0.14, P < 0.05] and inpatient FMT (OR = 0.19, P < 0.05) were each independently inversely related to FMT success. There were 35 (32%) patients younger than 60 years of age, and 14 (40%) of them had a background of inflammatory bowel disease. CONCLUSION: FMT is a safe and effective treatment for CDI, with capsules emerging as a successful and well-tolerated route. Severe CDI is less likely to respond to FMT.


Subject(s)
Clostridioides difficile/isolation & purification , Clostridium Infections/therapy , Diarrhea/therapy , Fecal Microbiota Transplantation/methods , Aged , Aged, 80 and over , Capsules , Clostridium Infections/diagnosis , Clostridium Infections/microbiology , Diarrhea/diagnosis , Diarrhea/microbiology , Fecal Microbiota Transplantation/instrumentation , Female , Humans , Israel , Male , Middle Aged , Recurrence , Retrospective Studies , Severity of Illness Index , Treatment Outcome
7.
Rev. esp. enferm. dig ; 109(6): 473-476, jun. 2017. ilus
Article in English | IBECS | ID: ibc-163268

ABSTRACT

The use of fecal microbiota transplantation in recurrent Clostridium difficile infection and coexistent inflammatory bowel disease remains unclear. A 61-year-old man with ulcerative pancolitis was diagnosed with a third recurrence of Clostridium difficile infection, previously treated with metronidazole, vancomycin and fidaxomicin. Fecal microbiota transplantation of an unrelated healthy donor was performed by the lower route. After a twelve month follow-up, the patient remains asymptomatic without Clostridium difficile infection relapses or inflammatory bowel disease flare-ups. Fecal microbiota transplantation is relatively simple to perform, well-tolerated, safe and effective in recurrent Clostridium difficile infection with ulcerative pancolitis, as an alternative in case of antibiotic therapy failure (AU)


No disponible


Subject(s)
Humans , Male , Middle Aged , Fecal Microbiota Transplantation/instrumentation , Fecal Microbiota Transplantation/methods , Clostridioides difficile/isolation & purification , Recurrence , Inflammatory Bowel Diseases/complications , Inflammatory Bowel Diseases/diagnosis , Colitis/complications , Colitis/therapy , Colonoscopy/instrumentation , Colonoscopy/methods
8.
Z Gastroenterol ; 54(10): 1143-1146, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27644000

ABSTRACT

Fecal microbiota transplantation has gathered much attention due to its high efficacy in resolving recurrent Clostridium difficile infection. Until today, it is recognized as a safe procedure without any severe side effects. Patients with impaired conscious states suffering from recurrent episodes of aspiration are at increased risk by endoscopic interventions needed during standard approaches for fecal microbiota transplantation application.Here, we illustrate the case of a tetraplegic patient undergoing fecal microbiota transplantation due to his fifth recurrent episode of Clostridium difficile infection using a self-advancing nasal jejunal feeding tube as effective minimal-invasive option of fecal microbiota transplantation application. Persistent aggravation of arterial hypertension, which developed post-intervention in this patient, could be interpreted as a hitherto unknown side effect of fecal microbiota transplantation in this setting. Moreover, this is a further hint for a link between the intestinal microbiome and arterial hypertension in general.


Subject(s)
Clostridioides difficile , Enteral Nutrition , Enterocolitis, Pseudomembranous/therapy , Fecal Microbiota Transplantation/instrumentation , Fecal Microbiota Transplantation/methods , Hypertension/etiology , Aged, 80 and over , Enterocolitis, Pseudomembranous/diagnosis , Enterocolitis, Pseudomembranous/microbiology , Equipment Design , Equipment Failure Analysis , Fecal Microbiota Transplantation/adverse effects , Humans , Hypertension/diagnosis , Hypertension/prevention & control , Male , Recurrence , Treatment Outcome
9.
Methods Mol Biol ; 1476: 259-67, 2016.
Article in English | MEDLINE | ID: mdl-27507347

ABSTRACT

Clostridium difficile is a challenging infection that can be difficult to treat with antibiotic therapy. This chapter outlines the processing material for fecal microbiota transplantation (FMT), also known as stool transplant. Fecal transplantations are effective in treating recurrent C. difficile infection (CDI). FMT uses a stool sample collected from a healthy, screened donor to restore healthy microbiota in the colon of a patient with CDI for symptom resolution. Here, we describe a rapid method for FMT preparation that uses inexpensive and disposable materials.


Subject(s)
Clostridioides difficile/pathogenicity , Enterocolitis, Pseudomembranous/therapy , Fecal Microbiota Transplantation/methods , Clostridioides difficile/physiology , Colon/microbiology , Colon/pathology , Enterocolitis, Pseudomembranous/microbiology , Enterocolitis, Pseudomembranous/pathology , Fecal Microbiota Transplantation/instrumentation , Feces/microbiology , Gastrointestinal Microbiome/physiology , Humans , Patient Selection/ethics , Tissue Donors/ethics
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