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1.
Int Urogynecol J ; 32(5): 1151-1156, 2021 May.
Article in English | MEDLINE | ID: mdl-32696187

ABSTRACT

INTRODUCTION AND HYPOTHESIS: The aim of this study was to assess the impact of botulinum toxin injection in women with myofascial pelvic pain (MFPP) syndrome of the pelvic floor who had failed conservative treatment. METHODS: This was a retrospective descriptive observational study of 48 consecutive patients receiving botulinum toxin to the pelvic floor for MFPP syndrome in a tertiary teaching hospital over an 8-year period. Trigger points were identified, and botulinum toxin was injected into the pelvic floor at the trigger points in doses ranging from 50 to 200 units. The patient-reported global impression of improvement scale was used to evaluate the success at follow-up, and adverse effects were recorded. RESULTS: Forty-six women attended for follow-up at 3-6 months. Of these, 34 (74%) reported an improvement in their symptoms (slightly better, much better, very much better), 12 (26%) had no change, and no patients reported worsening of symptoms. One patient (2%) reported transient postoperative faecal incontinence, which resolved after 2 weeks. There appeared to be no difference in outcome between the doses. CONCLUSIONS: Botulinum toxin injection into the pelvic floor of women with MFPP appears to be beneficial in those who have failed conservative treatment. Prospective studies, including dose-finding studies, are now required.


Subject(s)
Botulinum Toxins, Type A , Myofascial Pain Syndromes , Neuromuscular Agents , Female , Humans , Pain Measurement , Pelvic Pain , Prospective Studies , Retrospective Studies , Treatment Outcome
2.
Post Reprod Health ; 21(4): 151-7, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26545976

ABSTRACT

OBJECTIVE: In 2010, our hospital, in line with National guidance, changed advice on antibiotic prescribing for UTI to reduce use of cephalosporins in favour of penicillins. We hypothesized that this change in policy would have no impact on the pattern of antibiotic resistance of the organisms causing UTI. STUDY DESIGN: Audit review of all urine samples sent to BWH from 2009 to 2013 and positive cultures showing Enterobacteriaceae were then tested for antibiotic susceptibility. RESULTS: There has been an increase in the resistance of both Co-amoxiclav and Ciprofloxacin since 2009. Co-amoxiclav and trimethoprim now have similar resistance rates. Ciprofloxacin resistance has risen fairly quickly in the last four years from 1% to 8%. Resistance to nitrofurantoin has remained low. Gentamicin resistance remained stable and very low, second best to meroponem. IMPACT: The results have been fed back to commissioners and internally and are being used as part of the guideline updating process. CONCLUSIONS: Hospital protocols for treating infections should be reviewed and updated based on accurate local data. These data should be used for formulating regional specific protocols. Our results suggest that meroponem and ciprofloxacin should be reserved for microbiologically proven resistance to other antibiotics.


Subject(s)
Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial , Enterobacteriaceae Infections/drug therapy , Enterobacteriaceae/drug effects , Urinary Tract Infections/drug therapy , Amoxicillin-Potassium Clavulanate Combination/pharmacology , Ciprofloxacin/pharmacology , Clinical Audit , England , Female , Gentamicins/pharmacology , Health Policy , Humans , Meropenem , Microbial Sensitivity Tests , Nitrofurantoin/pharmacology , Practice Guidelines as Topic , Thienamycins/pharmacology , Trimethoprim/pharmacology , Urinary Tract Infections/microbiology
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