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EONS Poster diplay

3736 - EONS Poster - “It may not affect you” -- Lived experiences and support needs of women who developed peripheral neuropathy following chemotherapy treatment for cancer.

Date

22 Oct 2018

Session

EONS Poster diplay

Topics

Management of Systemic Therapy Toxicities;  Supportive Care and Symptom Management

Tumour Site

Presenters

Mary Tanay

Citation

Annals of Oncology (2018) 29 (suppl_8): viii698-viii701. 10.1093/annonc/mdy278

Authors

M.A. Tanay1, J. Armes2

Author affiliations

  • 1 Faculty Of Nursing, Midwifery And Palliative Care, King's College London, Se1 8WA - London/GB
  • 2 Faculty Of Health And Medical Sciences, University of Surrey, GU2 7XH - Surrey/GB

Resources

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Abstract 3736

Background

Some cancer drugs cause chemotherapy-induced peripheral neuropathy (CIPN) or damage to the nerves. CIPN affects the hands and feet, with patients reporting symptoms such as numbness, tingling, pain and muscle weakness. The nature of symptoms depends on the chemotherapy agents and drug dose that patients receive. Options to minimise the severity of symptoms may involve dose reduction, delay or discontinuation of chemotherapy. This study explored lived experiences of women who developed peripheral neuropathy following cancer chemotherapy treatment.

Methods

The study was conducted in the United Kingdom and was advertised through cancer charity websites and social media accounts. Using set eligibility criteria, purposeful convenience sampling was carried out. Women diagnosed with breast or ovarian cancer who experienced or are still experiencing neuropathy following chemotherapy treatment were recruited. Semi-structured recorded telephone interviews were conducted (n = 15). Interpretative phenomenological analysis (IPA) was used to analyse data.

Results

The analysis resulted to four main themes: struggle to process CIPN information, information and trust when making treatment decisions, experience of symptom reporting and challenges of mitigating CIPN symptoms. Similar to previous studies, participants used analogies to describe CIPN symptoms such as ‘like walking on pebbles, sand, needles or gravel’.

Conclusions

Findings suggest that interventions to improve understanding of CIPN symptoms by patients and clinicians are needed in practice. A broader insight of patients’ experiences of CIPN helps progress development of interventions to enhance communication, assessment and management of CIPN symptoms.

Clinical trial identification

Legal entity responsible for the study

King's College London.

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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