Literature DB >> 22597705

Feasibility of evaluating quality cancer care using registry data and electronic health records: a population-based study.

Adele Caldarella1, Gianni Amunni, Catia Angiolini, Emanuele Crocetti, Francesco Di Costanzo, Angelo Di Leo, Francesco Giusti, Andrea Lopes Pegna, Paola Mantellini, Lucio Luzzatto, Eugenio Paci.   

Abstract

OBJECTIVE: To evaluate the quality of patients care, a set of indicators of the standards of cancer care were defined. PARTICIPANTS: We developed a set of indicators to assess the implementation in daily practice of recommendation produced by a regional network (Istituto Toscano Tumori). This set was tested in a retrospective study in the resident population of the Tuscany Region; the regional health system is organized on 12 local health authorities which refer to three macro areas (Area Vasta). The study included incident colorectal, lung and breast cancer cases listed in 2004 for the Tuscan Cancer Registry, a population-based registry which collected tumor cases diagnosed in all residents in Tuscany. Electronic data from registry database were used to determine the compliance with each indicator for patients in 2004. To validate the results, an ad hoc clinical survey including the same geographical area for the year 2006 was performed. INTERVENTION: None. MAIN OUTCOME MEASURES: The proportion of patients who fulfilled each of the indicators.
RESULTS: Our study showed the feasibility of the evaluation of the quality of cancer care using cancer registry population-based data and major computerized information systems. The estimation of the selected indicators confirmed a good homogeneity among areas, and globally revealed a good intraregional performance.
CONCLUSIONS: Further work is needed to develop specific quality measures, particularly about structural data and to continually revise indicators of quality of care. Data from a cancer registry, however, can be useful to evaluate quality of cancer care.

Entities:  

Mesh:

Year:  2012        PMID: 22597705     DOI: 10.1093/intqhc/mzs020

Source DB:  PubMed          Journal:  Int J Qual Health Care        ISSN: 1353-4505            Impact factor:   2.038


  6 in total

1.  New accountability, new challenges: improving treatment reporting to a tumor registry.

Authors:  Nina A Bickell; Jill Wellner; Rebeca Franco; Ann Scheck McAlearney
Journal:  J Oncol Pract       Date:  2013-05       Impact factor: 3.840

Review 2.  Benchmarking and audit of breast units improves quality of care.

Authors:  P A van Dam; L Verkinderen; J Hauspy; P Vermeulen; L Dirix; M Huizing; S Altintas; K Papadimitriou; M Peeters; W Tjalma
Journal:  Facts Views Vis Obgyn       Date:  2013

3.  Compliance with clinical guidelines for breast cancer management: A population-based study of quality-of-care indicators in France.

Authors:  Anne Cowppli-Bony; Brigitte Trétarre; Emilie Marrer; Gautier Defossez; Laetitia Daubisse-Marliac; Gaelle Coureau; Pamela Minicozzi; Anne-Sophie Woronoff; Patricia Delafosse; Florence Molinié
Journal:  PLoS One       Date:  2019-10-23       Impact factor: 3.240

Review 4.  Quality indicators for radiation oncology.

Authors:  Susan V Harden; Kim-Lin Chiew; Jeremy Millar; Shalini K Vinod
Journal:  J Med Imaging Radiat Oncol       Date:  2022-03       Impact factor: 1.667

5.  Analysis and visualization of disease courses in a semantically-enabled cancer registry.

Authors:  Angel Esteban-Gil; Jesualdo Tomás Fernández-Breis; Martin Boeker
Journal:  J Biomed Semantics       Date:  2017-09-29

6.  Electronic health records and patient registries in medical oncology departments in Spain.

Authors:  N Ribelles; I Alvarez-Lopez; A Arcusa; J I Chacon; J de la Haba; J García-Corbacho; J Garcia-Mata; C Jara; J M Jerez; M Lázaro-Quintela; L Leon-Mateos; N Ramirez-Merino; A Tibau; A Garcia-Palomo
Journal:  Clin Transl Oncol       Date:  2021-04-17       Impact factor: 3.405

  6 in total

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