Evidence map›Paper›PMID 26608635›Full record

ArticleBMJ open2015

Bereaved relatives' experiences during the incurable phase of cancer: a qualitative interview study.

Marleen N Wijnhoven, Wim E Terpstra, Ronald van Rossem, Carolien Haazer, Nicolette Gunnink-Boonstra, Gabe S Sonke, Hilde M Buiting

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In one paragraph

Article in BMJ open, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Marleen N WijnhovenDepartment of Registry & Research, Netherlands Comprehensive Cancer Organization, Utrecht, The Netherlands Department of Clinical Psychology, VU University, Amsterdam, The Netherlands.
Wim E TerpstraDepartment of Internal Medicine, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.
Ronald van RossemDepartment of Pulmonology, Reinier de Graafgroep, Delft, The Netherlands.
Carolien HaazerDepartment of Internal Medicine, Reinier de Graafgroep, Delft, The Netherlands.
Nicolette Gunnink-BoonstraDepartment of Internal Medicine, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.
Gabe S SonkeDepartment of Registry & Research, Netherlands Comprehensive Cancer Organization, Utrecht, The Netherlands Division of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Hilde M BuitingDepartment of Registry & Research, Netherlands Comprehensive Cancer Organization, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine bereaved relatives' experiences from time of diagnosis of incurable cancer until death with specific emphasis on their role in the (end-of-life) decision-making concerning chemotherapy.

designQualitative interview study.

settingHospital-based. PARTICIPANTS AND

methodsIn-depth interviews with 15 close relatives of patients who died from non-small cell lung cancer or pancreatic cancer, using a thematic content analysis.

resultsAll relatives reported that patients' main reason to request chemotherapy was the possibility to prolong life. Relatives reported that patients receiving chemotherapy had more difficulty to accept the incurable nature of their disease than patients who did not. They mostly followed the patients' treatment wish and only infrequently suggested ceasing chemotherapy (because of side effects) despite sometimes believing that this would be a better option. Relatives continuously tried to support the patient in either approaching the death or in attaining hope to continue life satisfactorily. Most relatives considered the chemotherapy period meaningful, since it sparked patients' hope and was what patients wanted. Cessation of chemotherapy caused a relief but coincided with physical deterioration and an increased caregivers' role; many relatives recalled this latter period as more burdensome.

conclusionsRelatives tend to follow patients' wish to continue or cease chemotherapy, without expressing their own feelings, although they were more inclined to opt cessation. They experience a greater caregiver role after cessation and their feelings of responsibility associated with the disease can be exhausting. More attention is needed to reduce relatives' distress at the end of life, also to fully profit from this crucial form of (informal) healthcare.

Indexed as

BereavementNeoplasmsCaregiversFamilyFemaleHumansInterviews as TopicMaleMiddle AgedQualitative ResearchTerminal CareCHEMOTHERAPYETHICS (see Medical Ethics)MEDICAL ETHICSONCOLOGYPALLIATIVE CARE

Identifiers

PMID26608635
PMCPMC4663398

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