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1.
Clin Microbiol Infect ; 21(1): 48-53, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25636927

ABSTRACT

Clostridium difficile infection is one of the most common nosocomial infections. Among other alternatives to standard treatment with vancomycin for recurrent infection are faecal microbiota transplantation and rectal bacteriotherapy with a fixed mixture of intestinal bacterial strains isolated from faeces of healthy persons to mimic a theoretical normal microflora. Developed by Dr. Tvede and Dr. Rask-Madsen, the latter method has been in use for selected patients during the last 25 years in Denmark. In this study we reviewed the medical records of patients treated with rectal bacteriotherapy for relapsing C. difficile in Denmark, 2000-2012. The primary end point was recurrent diarrhoea within 30 days after treatment. A total of 55 patients were included in this case series. Thirty-five patients (64%) had no recurrence within 30 days of bacteriotherapy. Patients with recurrence tended to be older (75.8 years vs. 61.3 years; p 0.26), and more often have preexisting gastrointestinal illness and longer duration of time from the first CDI to bacteriotherapy (221.6 days vs. 175.3 days; p 0.18). Treatment success was 80% in the subgroup of patients with no known gastrointestinal illness and first C. difficile episode less than 6 months before bacteriotherapy. The most common adverse events were abdominal pain (10.9%) and worsening diarrhoea (4.3%). One patient was hospitalized 10 days after treatment with appendicitis, fever, and Escherichia coli bacteremia. The results from this study indicate that rectal bacteriotherapy is a viable alternative to faecal microbiota transplantation in patients with relapsing C. difficile-associated diarrhoea.


Subject(s)
Biological Therapy/methods , Clostridioides difficile , Clostridium Infections/therapy , Feces/microbiology , Adult , Aged , Aged, 80 and over , Bacteria , Clostridium Infections/epidemiology , Denmark/epidemiology , Female , Hospitalization/statistics & numerical data , Humans , Male , Middle Aged , Recurrence , Retrospective Studies , Risk Factors , Treatment Outcome , Young Adult
2.
BJOG ; 115(11): 1405-10, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18717669

ABSTRACT

OBJECTIVE: The objective of this study was to examine whether the use of nicotine replacement therapy (NRT) during pregnancy increases the risk of stillbirth. DESIGN: Cohort study with prospective data. SETTING: Denmark 1996-2002. POPULATION: A total of 87,032 singleton pregnancies enrolled in the Danish National Birth Cohort for which information on NRT use as well as smoking was available. METHODS: Outcome of pregnancy was identified by register linkage, with <1% loss to follow up. We conducted Cox regression analyses to estimate the hazard ratio (HR) and 95% CI of stillbirth according to the use of NRT, type of NRT use and a combination of NRT use and smoking. MAIN OUTCOME MEASURES: Stillbirth, defined as delivery of a dead fetus after 20 completed weeks of gestation. RESULTS: A total of 495 pregnancies (5.7 in 1000 births) ended in stillbirth, 8 of which were among NRT users (4.2 in 1000 births). After adjustment for confounders, women who used NRT during pregnancy had a HR of 0.57 (95% CI 0.28-1.16) for stillbirth compared with those who did not use NRT. Smoking during pregnancy was associated with an increased risk of stillbirth (HR 1.46, 95% CI 1.17-1.82), while women who both smoked and used NRT had a HR of 0.83 (95% CI 0.34-2.00) compared with nonsmoking women who did not use NRT. CONCLUSION: Our study does not indicate that use of NRT during pregnancy increases the risk of stillbirth.


Subject(s)
Nicotine/adverse effects , Nicotinic Agonists/adverse effects , Pregnancy Complications/etiology , Smoking Prevention , Stillbirth , Adult , Cohort Studies , Denmark/epidemiology , Female , Humans , Maternal Age , Nicotine/administration & dosage , Nicotinic Agonists/administration & dosage , Pregnancy , Pregnancy Complications/epidemiology , Pregnancy Complications/prevention & control , Risk Factors , Smoking/adverse effects , Smoking/epidemiology
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