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Using Process Indicators to Monitor Documentation of Patient-Centred Variables in an Integrated Oncology and Palliative Care Pathway-Results from a Cluster Randomized Trial.
Hjermstad, Marianne Jensen; Hamfjord, Julian; Aass, Nina; Dajani, Olav; Lundeby, Tonje; Wester, Torunn; Kaasa, Stein.
Afiliação
  • Hjermstad MJ; Department of Oncology, Oslo University Hospital, 4950 Oslo, Norway.
  • Hamfjord J; European Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, 4956 Oslo, Norway.
  • Aass N; Institute of Clinical Medicine, University of Oslo, 0318 Oslo, Norway.
  • Dajani O; Department of Oncology, Oslo University Hospital, 4950 Oslo, Norway.
  • Lundeby T; Faculty of Medicine, University of Oslo, 0372 Oslo, Norway.
  • Wester T; Department of Oncology, Oslo University Hospital, 4950 Oslo, Norway.
  • Kaasa S; European Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, 4956 Oslo, Norway.
Cancers (Basel) ; 13(9)2021 May 03.
Article em En | MEDLINE | ID: mdl-34063594
ABSTRACT

BACKGROUND:

Despite robust evidence from randomized controlled trials (RCTs) demonstrating clinical and patient-reported benefits of integrated oncology and palliative care, the tumour-centred focus is predominant. This single-centre process evaluation monitors documentation of required patient-centred variables during an RCT.

METHODS:

Performance status, patient self-reported symptoms, weight and summaries to general practitioners were assessed from June 2017 to July 2020 in three consultation types first oncological after study inclusion and palliative and oncological consultations during chemotherapy. Descriptive statistics were used to monitor if the pre-defined program fulfilment of ≥85% documentation was reached.

RESULTS:

435 consultations were monitored in 76 patients; 60.5% males, 86.8% with GI cancers; 76 (17.5%) were from the first oncological consultations, 87 (20.0%) and 272 (62.5%) from palliative or subsequent oncological consultations. Program fulfilment differed across consultation types with 94.8% in the palliative consultations (83.3-100%), relative to 65.8% (62.5-75.0%) and 69.2% (57.0-84.3%) for first and subsequent oncological consultations over time, respectively. Use of self-reported symptoms was consistently lower in the oncological consultations.

CONCLUSIONS:

The documentation level of required core variables was not satisfactory, notwithstanding their high clinical relevance and continuous reminders during study. Pre-trial optimization strategies are paramount to promote integration and reduce professional and personal barriers towards a more patient-centred focus.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Ano de publicação: 2021 Tipo de documento: Article