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1.
Prog Urol ; 32(5): 319-325, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34920919

ABSTRACT

AIMS: Evaluation of repeated (at least 4) intra-detrusor injections of toxin botulinum A (IDI-TBA) for neurogenic bladder in a pediatric cohort. METHODS: Patients who underwent at least 4 IDI-TBA between 2005 and 2017 for neurogenic bladder related issues were included (detrusor overactivity and low compliance). Clinical and cystometric data were collected before and after the first injection and after the last injection. The primary endpoint was the proportion of patients with non-abnormal cystometry (no detrusor overactivity and normal compliance). Secondary outcomes were the evolution of the observed bladder capacity/expected ratio, surgical complications and acquired kidney impairment. RESULTS: From the 832 patients referred to our institution for neurogenic bladder, 48 underwent IDI-TBA, and 17 at least 4 injections. Among them, a total of 95 procedures were performed (median per patient 5 [4-8]). While the first injection had a significant effect for 82.3% patients, the last injection improved the medical condition for only 53.0% cases. The bladder capacity ratio, initially 36.1%, increased to 80.3% after the first injection but decreased to a level of 57.1% at last. After a median follow-up of 57 [34-102] months, no severe complications were reported but 11.8% of patients presented with repeated pyelonephritis. A bladder augmentation surgery was finally indicated for 35.3% cases. CONCLUSIONS: Despite a low complication rate and impressive cystometric results after the first injection, IDI-TBA efficacy decreased with time and repetition. These findings prone a long-term follow-up and a "à-la-carte" management of this specific population depending on the long-term response to IDI-TBA.


Subject(s)
Botulinum Toxins, Type A , Neuromuscular Agents , Urinary Bladder, Neurogenic , Urinary Bladder, Overactive , Administration, Intravesical , Botulinum Toxins, Type A/therapeutic use , Child , Female , Humans , Injections , Male , Neuromuscular Agents/adverse effects , Treatment Outcome , Urinary Bladder, Neurogenic/drug therapy , Urinary Bladder, Neurogenic/etiology , Urinary Bladder, Overactive/complications , Urinary Bladder, Overactive/drug therapy , Urodynamics
4.
Chromosome Res ; 9(6): 437-48, 2001.
Article in English | MEDLINE | ID: mdl-11592478

ABSTRACT

Extensive chromosome variation involving Robertsonian and non-Robertsonian changes were proposed to explain chromosomal evolution within killifishes of the aplocheiloid group belonging to the order Cyprinodontiforms. In the present work we describe the karyotypes of four Cynolebias species and analyze chromosome changes by means of mitochondrial phylogenetic studies, including 10 taxa of this genus. Diploid numbers varied from 48 to 44 and the number of chromosome arms from 50 to 54. Molecular phylogenetic analyses allow us to corroborate previous hypothesis about chromosome evolution in aplocheiloid fishes. The tree topology based on a combined dataset of mitochondrial cytochrome b and 12S genes shows that recent cladogenetic events within the genus Cynolebias could have occurred by allopatric or 'in-situ' differentiation involving chromosomal rearrangements. Our analyses of approximately 10% of mitochondrial genome can be helpful in determining these recent cladogenetic events but it showed limited phylogenetic resolution at intermediate levels of divergence. This can be explained in part by the high levels of DNA sequence divergence (ranging from 0.015 to 0.245) detected at intrageneric level. Different methodological approaches suggest that chromosomal changes in Cynolebias have occurred during their differentiation, supporting the hypothesis that the unresolved basal polytomy could be the result of rapid speciation events, like a true 'star polytomy'.


Subject(s)
Chromosomes/genetics , Killifishes/genetics , Mitochondria/genetics , Animals , Chromosome Banding , Cytochrome b Group/genetics , DNA, Mitochondrial/analysis , Evolution, Molecular , Karyotyping , Killifishes/classification , Phylogeny , RNA, Ribosomal/genetics
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