1.Success and Complication Rates After Sacral Neuromodulation for Fecal Incontinence and Constipation: A Single-center Follow-up Study
Bernhard WIDMANN ; Christian GALATA ; Rene WARSCHKOW ; Ulrich BEUTNER ; Onder ÖGREDICI ; Franc H HETZER ; Bruno M SCHMIED ; Stefan POST ; Lukas MARTI
Journal of Neurogastroenterology and Motility 2019;25(1):159-170
BACKGROUND/AIMS: The aim of this study was to evaluate the sustainability of sacral neuromodulation (SNM) success in patients with fecal incontinence (FI) and/or constipation. METHODS: This is a retrospective analysis of a prospective database of patients who received SNM therapy for FI and/or constipation between 2006 and 2015. Success rates, complications and reintervention rates were assessed after up to 10 years of follow-up. RESULTS: Electrodes for test stimulation were implanted in 101 patients, of whom 79 (78.2%) received permanent stimulation. The mean follow-up was 4.4 ± 3.0 years. At the end of follow-up, 57 patients (72.2%) were still receiving SNM. The 5-year success rate for FI and isolated constipation was 88.2% (95% confidence interval [CI], 80.1–97.0%) and 31.2% (95% CI, 10.2–95.5%), respectively (P < 0.001). In patients with FI, involuntary evacuations per week decreased > 50% in 76.1% of patients (95% CI, 67.6–86.2%) after 5 years. A lead position at S3 was associated with an improved outcome (P = 0.04). Battery exchange was necessary in 23 patients (29.1%), with a median battery life of 6.2 years. Reinterventions due to complications were necessary in 24 patients (30.4%). For these patients, the 5-year success rate was 89.0% (95% CI, 75.3–100.0%) compared to 78.4% (95% CI, 67.2–91.4%) for patients without reintervention. CONCLUSIONS: SNM offers an effective sustainable treatment for FI. For constipation, lasting success of SNM is limited and is thus not recommended. Reinterventions are necessary but do not impede treatment success.
Constipation
;
Electric Stimulation
;
Electrodes
;
Fecal Incontinence
;
Follow-Up Studies
;
Humans
;
Prospective Studies
;
Retrospective Studies
2.Integrating Culture-based Antibiotic Resistance Profiles with Whole-genome Sequencing Data for 11,087 Clinical Isolates.
Valentina GALATA ; Cédric C LACZNY ; Christina BACKES ; Georg HEMMRICH-STANISAK ; Susanne SCHMOLKE ; Andre FRANKE ; Eckart MEESE ; Mathias HERRMANN ; Lutz VON MÜLLER ; Achim PLUM ; Rolf MÜLLER ; Cord STÄHLER ; Andreas E POSCH ; Andreas KELLER
Genomics, Proteomics & Bioinformatics 2019;17(2):169-182
Emerging antibiotic resistance is a major global health threat. The analysis of nucleic acid sequences linked to susceptibility phenotypes facilitates the study of genetic antibiotic resistance determinants to inform molecular diagnostics and drug development. We collected genetic data (11,087 newly-sequenced whole genomes) and culture-based resistance profiles (10,991 out of the 11,087 isolates comprehensively tested against 22 antibiotics in total) of clinical isolates including 18 main species spanning a time period of 30 years. Species and drug specific resistance patterns were observed including increased resistance rates for Acinetobacter baumannii to carbapenems and for Escherichia coli to fluoroquinolones. Species-level pan-genomes were constructed to reflect the genetic repertoire of the respective species, including conserved essential genes and known resistance factors. Integrating phenotypes and genotypes through species-level pan-genomes allowed to infer gene-drug resistance associations using statistical testing. The isolate collection and the analysis results have been integrated into GEAR-base, a resource available for academic research use free of charge at https://gear-base.com.
Acinetobacter baumannii
;
genetics
;
isolation & purification
;
Bacteria
;
genetics
;
isolation & purification
;
Cell Culture Techniques
;
methods
;
Drug Resistance, Microbial
;
genetics
;
Escherichia coli
;
genetics
;
isolation & purification
;
Genome, Bacterial
;
Genotype
;
Humans
;
Internet
;
Microbial Sensitivity Tests
;
Phenotype
;
Whole Genome Sequencing

Result Analysis
Print
Save
E-mail