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The Validity of Registered Synchronous Peritoneal Metastases from Colorectal Cancer in the Danish Medical Registries.
Ravn, Sissel; Christiansen, Christian F; Hagemann-Madsen, Rikke H; Verwaal, Victor J; Iversen, Lene H.
Afiliação
  • Ravn S; Department of Surgery, Aarhus University Hospital, Aarhus, Denmark.
  • Christiansen CF; Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.
  • Hagemann-Madsen RH; Department of Pathology, Lillebaelt Hospital, Vejle, Denmark.
  • Verwaal VJ; Department of Surgery, Aarhus University Hospital, Aarhus, Denmark.
  • Iversen LH; Department of Surgery, Aarhus University Hospital, Aarhus, Denmark.
Clin Epidemiol ; 12: 333-343, 2020.
Article em En | MEDLINE | ID: mdl-32273772
ABSTRACT

INTRODUCTION:

Treatment options for peritoneal metastases (PM) from colorectal cancer (CRC) have increased, their efficiency should be monitored. For this purpose, register-based data on PM can be used, if valid.

PURPOSE:

We aimed to evaluate the completeness and positive predictive value (PPV) of synchronous peritoneal metastases (S-PM) registered among CRC patients in the Danish National Patient Register (DNPR) and/or the Danish National Pathology Register (the DNPatR) using the Danish Colorectal Cancer Group database (DCCG) as a reference. PATIENTS AND

METHODS:

We identified Danish patients with newly diagnosed primary CRC in the DCCG during 2014-2015. S-PM were routinely registered in the DCCG. We excluded patients with non-CRC cancers and identified S-PM using all three registries. We estimated the completeness and the PPV of registered S-PM in the DNPR, the DNPatR and the DNPR and/or the DNPatR (DNPR/DNPatR) in combination using the DCCG as the reference. We stratified by age, gender, WHO performance status, tumour location and distant metastases to liver and/or lungs.

RESULTS:

We identified 9142 patients with CRC in DCCG. In DCCG, 366 patients were registered with S-PM, among whom 213 in DCCG only, whereas 153 in DCCG and in at least one of DNPR and/or DNPatR. In DNPR/DNPatR, S-PM was registered with a completeness of 42% [95% CI 37-47] and a PPV of 60% [95% CI 54-66]. In the DNPR only, the completeness was 32% [95% CI 27-37] and the PPV 57% [95% CI 50-64]. The completeness in the DNPatR was 19% [95% CI 15-23] and the PPV was 76% [95% CI 68-85]. In the DNPR/DNPatR patients aged <60 years (57% [95% CI 46-69]), patients with WHO performance status 0 (46% [95% CI 37-54]) and patients with no distant metastases (58% [95% CI 50-65]) were registered with a higher completeness.

CONCLUSION:

Our algorithm demonstrates that the DNPR/DNPatR captures less than half of CRC patients with S-PM. Potential candidates for curative treatment options are registered with a higher completeness. Clinicians should be encouraged to register the presence of S-PM to increase the validity of register-based S-PM data.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article