Details der Publikation - Development of a North American coordinated registry network for surgical treatment of benign prostatic hyperplasia

Development of a North American coordinated registry network for surgical treatment of benign prostatic hyperplasia

Purpose To create a prospective, multicenter coordinated registry network (CRN) of robust “real world” data for benign prostatic hyperplasia (BPH) that links surgical practices to objective and subjective outcomes of patients who undergo surgery for the improvement in lower urinary tract symptoms (LUTS) secondary to BPH. Methods We gathered a group of BPH experts from various institutions to identify the minimum core data elements needed to assess BPH procedures. To achieve consensus on the data elements, we used a Delphi method adaptation, in which a series of surveys were answered by the expert panel individually and anonymously. Survey results were collected and analyzed. Questions for the following round were based on response analysis from the prior survey. This process was repeated until consensus was achieved. Results Participation rates in the first and second rounds were 100% and 90%, respectively. The expert panel reached consensus on 148 data elements out of the 182 proposed, capturing patient medical and surgical history, procedure, discharge, short- and long-term follow-up, device factors, surgery, and surgeon factors. Conclusion We have successfully developed a set of core data elements to support the study of BPH surgical therapies by gathering an expert panel on BPH and using the Delphi method. These data elements influence provider decisions about treatment and include important outcomes related to efficacy and safety..

Medienart:	E-Artikel

Erscheinungsjahr:	2022
Erschienen:	2022

Enthalten in:	Zur Gesamtaufnahme - volume:40
Enthalten in:	World journal of urology - 40(2022), 12 vom: 11. Okt., Seite 2991-2999

Sprache:	Englisch

Beteiligte Personen:	Martinez Diaz, Susana [VerfasserIn] Bhojani, Naeem [VerfasserIn] Elterman, Dean [VerfasserIn] Zorn, Kevin [VerfasserIn] Kaplan, Steven A. [VerfasserIn] Kohler, Tobias S. [VerfasserIn] Lerner, Lori B. [VerfasserIn] McVary, Kevin T. [VerfasserIn] Rutman, Matthew P. [VerfasserIn] Welliver, Charles [VerfasserIn] Te, Alexis E. [VerfasserIn] Sedrakyan, Art [VerfasserIn] Chughtai, Bilal [VerfasserIn]

Links:	Volltext [lizenzpflichtig]

Themen:	Benign prostatic hyperplasia surgical treatment Coordinated registry network Lower urinary tract symptoms Multicenter

RVK:	RVK Klassifikation ELIB24

Anmerkungen:	© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022

doi:	10.1007/s00345-022-04164-3

funding:
Förderinstitution / Projekttitel:

PPN (Katalog-ID):	OLC2132918317

Internformat


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520			\|a Purpose To create a prospective, multicenter coordinated registry network (CRN) of robust “real world” data for benign prostatic hyperplasia (BPH) that links surgical practices to objective and subjective outcomes of patients who undergo surgery for the improvement in lower urinary tract symptoms (LUTS) secondary to BPH. Methods We gathered a group of BPH experts from various institutions to identify the minimum core data elements needed to assess BPH procedures. To achieve consensus on the data elements, we used a Delphi method adaptation, in which a series of surveys were answered by the expert panel individually and anonymously. Survey results were collected and analyzed. Questions for the following round were based on response analysis from the prior survey. This process was repeated until consensus was achieved. Results Participation rates in the first and second rounds were 100% and 90%, respectively. The expert panel reached consensus on 148 data elements out of the 182 proposed, capturing patient medical and surgical history, procedure, discharge, short- and long-term follow-up, device factors, surgery, and surgeon factors. Conclusion We have successfully developed a set of core data elements to support the study of BPH surgical therapies by gathering an expert panel on BPH and using the Delphi method. These data elements influence provider decisions about treatment and include important outcomes related to efficacy and safety.
650		4	\|a Coordinated registry network
650		4	\|a Multicenter
650		4	\|a Benign prostatic hyperplasia surgical treatment
650		4	\|a Lower urinary tract symptoms
700	1		\|a Bhojani, Naeem \|4 aut
700	1		\|a Elterman, Dean \|4 aut
700	1		\|a Zorn, Kevin \|4 aut
700	1		\|a Kaplan, Steven A. \|4 aut
700	1		\|a Kohler, Tobias S. \|4 aut
700	1		\|a Lerner, Lori B. \|4 aut
700	1		\|a McVary, Kevin T. \|4 aut
700	1		\|a Rutman, Matthew P. \|4 aut
700	1		\|a Welliver, Charles \|4 aut
700	1		\|a Te, Alexis E. \|4 aut
700	1		\|a Sedrakyan, Art \|4 aut
700	1		\|a Chughtai, Bilal \|0 (orcid)0000-0002-0515-2578 \|4 aut
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Development of a North American coordinated registry network for surgical treatment of benign prostatic hyperplasia

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