Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pakeeza A. Alam"'
Autor:
Katarzyna Bochenska, Robert E. Gutman, Charelle M. Carter-Brooks, Meadow M. Good, Pakeeza A. Alam, Jenifer N. Byrnes, Emily N. B. Myer, Eshetu Tefera, Emily R W Davidson, Maria E. Florian-Rodriguez
Publikováno v:
International Urogynecology Journal. 32:2135-2142
Women with hereditary disorders of connective tissue (HDCT) are at increased risk of pelvic organ prolapse (POP) and stress urinary incontinence (SUI). We hypothesized that patients would have increased incidence and severity of perioperative complic
Autor:
Emily R W, Davidson, Pakeeza A, Alam, Jenifer N, Byrnes, Katarzyna, Bochenska, Maria, Florian-Rodriguez, Charelle M, Carter-Brooks, Emily N B, Myer, Eshetu A, Tefera, Meadow M, Good, Robert E, Gutman
Publikováno v:
International urogynecology journal. 32(8)
Women with hereditary disorders of connective tissue (HDCT) are at increased risk of pelvic organ prolapse (POP) and stress urinary incontinence (SUI). We hypothesized that patients would have increased incidence and severity of perioperative complic
Autor:
Eshetu Tefera, Pakeeza A. Alam, Lee A. Richter, Brett A Clark, Linda S Burkett, Nicola C White
Publikováno v:
Female Pelvic Medicine & Reconstructive Surgery. 24:161-165
OBJECTIVE The objective of this study was to compare disposable pads to Icon™ reusable underwear for the management of urinary incontinence on dimensions of quality of life and product performance. METHODS This randomized cross-over trial included
Autor:
Cheryl B. Iglesia, Pakeeza A. Alam
Publikováno v:
Obstetrics and Gynecology Clinics of North America. 43:131-139
Informed consent is the process in which a patient makes a decision about a surgical procedure or medical intervention after adequate information is relayed by the physician and understood by the patient. This process is critical for reconstructive p
Autor:
Pakeeza A. Alam, Cheryl B. Iglesia
Publikováno v:
The Innovation and Evolution of Medical Devices ISBN: 9783319970721
The process for introducing new surgical devices differs from drug evaluations. The US Food and Drug Administration (FDA) often clears medical devices through the 510(k) process, which evaluates safety by substantial equivalence to another device. Ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35c157c21a0a6045be6cd2c022cfb2a8
https://doi.org/10.1007/978-3-319-97073-8_9
https://doi.org/10.1007/978-3-319-97073-8_9
Publikováno v:
Female pelvic medicinereconstructive surgery. 26(9)
Objective The objective of this study was to perform a cost analysis assessing the economic feasibility of reusable underwear as alternative for disposable pads for women with mild to moderate urinary incontinence. Methods A consumer-perspective cost