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Volumn 118, Issue 4, 2011, Pages 771-773

To mesh or not to mesh: Current debates in prolapse repair fueled by the u.s. food and drug administration safety notification

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL DECISION MAKING; CLINICAL EFFECTIVENESS; DEVICE APPROVAL; DEVICE RECALL; DEVICE SAFETY; EDITORIAL; FOLLOW UP; FOOD AND DRUG ADMINISTRATION; GOLD STANDARD; HUMAN; MESH SLING; OUTCOME ASSESSMENT; PELVIC ORGAN PROLAPSE; POSTERIOR INTRAVAGINAL SLINGPLASTY; PRIORITY JOURNAL; PROSTHESIS LOOSENING; PUBOVAGINAL SLING; REOPERATION; RETRACTOR; SACROCOLPOPEXY; STRESS INCONTINENCE; SURGICAL RISK; TISSUE GRAFT; TISSUE REPAIR;

EID: 80053372825     PISSN: 00297844     EISSN: None     Source Type: Journal    
DOI: 10.1097/AOG.0b013e318230b1f4     Document Type: Editorial
Times cited : (9)

References (10)
  • 1
    • 0031127072 scopus 로고    scopus 로고
    • Epidemiology of surgically managed pelvic organ prolapse and urinary incontinence
    • DOI 10.1016/S0029-7844(97)00058-6, PII S0029784497000586
    • Olsen AL, Smith VJ, Bergstrom JO, Colling JC, Clark AL. Epidemiology of surgically managed pelvic organ prolapse and urinary incontinence. Obstet Gynecol 1997;89:501-6. (Pubitemid 27133519)
    • (1997) Obstetrics and Gynecology , vol.89 , Issue.4 , pp. 501-506
    • Olsen, A.L.1    Smith, V.J.2    Bergstrom, J.O.3    Colling, J.C.4    Clark, A.L.5
  • 2
    • 80053355832 scopus 로고    scopus 로고
    • Epidemiologic evaluation of reoperation for surgically treated pelvic organ prolapse and urinary incontinence
    • Clark AL, Gregory T, Smith VJ, Edwards R. Epidemiologic evaluation of reoperation for surgically treated pelvic organ prolapse and urinary incontinence. Am J Obstet Gynecol 2001;184:1357-64.
    • (2001) Am J Obstet Gynecol , vol.184 , pp. 1357-1364
    • Clark, A.L.1    Gregory, T.2    Smith, V.J.3    Edwards, R.4
  • 6
    • 79955726540 scopus 로고    scopus 로고
    • Medical device recalls and the FDA approval process
    • Zuckerman DM, Brown P, Nissen SE. Medical device recalls and the FDA approval process. Arch Intern Med 2011;171:1006-11.
    • (2011) Arch Intern Med , vol.171 , pp. 1006-1011
    • Zuckerman, D.M.1    Brown, P.2    Nissen, S.E.3
  • 7
    • 79959309665 scopus 로고    scopus 로고
    • Medical device recalls: Get it right the first time: Comment on "medical device recalls and the FDA approval process
    • Redberg RF, Dhruva SS. Medical device recalls: get it right the first time: comment on "medical device recalls and the FDA approval process." Arch Intern Med 2011;171: 1011-2.
    • (2011) Arch Intern Med , vol.171 , pp. 1011-1012
    • Redberg, R.F.1    Dhruva, S.S.2
  • 8
    • 78149376593 scopus 로고    scopus 로고
    • Medical devices and the FDA approval process; Balancing safety and innovation; Comment on prevalence of fracture and fragment embolization of bard retrievable vena cava filters and clinical implications including cardiac perforation and tamponade
    • Redberg RF. Medical devices and the FDA approval process; balancing safety and innovation; comment on prevalence of fracture and fragment embolization of bard retrievable vena cava filters and clinical implications including cardiac perforation and tamponade. Arch Intern Med 2010;170:1831-3.
    • (2010) Arch Intern Med , vol.170 , pp. 1831-1833
    • Redberg, R.F.1
  • 10
    • 80053344124 scopus 로고    scopus 로고
    • American Urogynecologic Society Retrieved August 1, 2011
    • American Urogynecologic Society. AUGS response: FDA safety communication. Available at: https://www.augs.org/AUGSResponseFDASafetyAnnouncement/tabid/698/ Default. aspx. Retrieved August 1, 2011.
    • AUGS Response: FDA Safety Communication


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.