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Autologous myoblasts and fibroblasts versus collagen for treatment of stress urinary incontinence in women: a randomised controlled trial
Oleh:
Strasser, Hannes
;
Marksteiner, Rainer
;
Margreiter, Eva
;
Pinggera, Germar Michael
;
Mitterberger, Michael
;
Frauscher, Ferdinand
;
Ulmer, Hanno
;
Fussenegger, Martin
;
kofler, Kurt
;
Bartsch, Georg
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
The Lancet (keterangan: ada di Proquest) vol. 369 no. 9580 (Jun. 2007)
,
page 2179.
Ketersediaan
Perpustakaan FK
Nomor Panggil:
L01.K.2007.03
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Summary Background Preclinical studies have suggested that transurethral injections of autologous myoblasts can aid in regeneration of the rhabdosphincter, and fibroblasts in reconstruction of the urethral submucosa. We aimed to compare the effectiveness and tolerability of ultrasonography-guided injections of autologous cells with those of endoscopic injections of collagen for stress incontinence. Methods Between 2002 and 2004, we recruited 63 eligible women with urinary stress incontinence. 42 of these women were randomly assigned to receive transurethral ultrasonography-guided injections of autologous myoblasts and fibroblasts, and 21 to receive conventional endoscopic injections of collagen. The first primary outcome measure was an incontinence score (range 0-6) based on a 24-hour voiding diary, a 24-hour pad test, and a patient questionnaire. The other primary outcome measures were contractility of the rhabdosphincter and thickness of both the urethra and rhabdosphincter. Analysis was by intention to treat. This trial is registered with Controlled-Trials. com, number CCT¬NAPN-16630. Findings At 12-months' follow-up, 38 of the 42 women injected with autologous cells were completely continent, compared with two of the 21 patients given conventional treatment with collagen. The median incontinence score decreased from a baseline of6.0 (IQR 6.0-6.0; where 6 represents complete incontinence), to 0 (0-0) for patients treated with autologous cells, and 6.0 (3.5-6.0) for patients treated with collagen (p
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