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    AboutPolicies Privacy NoticeBlack Country Healthcare NHS Foundation TrustCoventry and Warwickshire Partnership NHS TrustDudley Group NHS Foundation TrustGeorge Eliot Hospital NHS TrustSandwell and West Birmingham NHS TrustSouth Warwickshire University NHS Foundation TrustUniversity Hospitals Birmingham NHS Foundation TrustUniversity Hospitals Coventry and Warwickshire NHS TrustWalsall Healthcare NHS Trust

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    Feasibility study of a randomised controlled trial of preoperative and postoperative nutritional supplementation in major lung surgery.

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    Author
    Kerr, Amy
    Lugg, Sebastian T
    Kadiri, Salma
    Swift, Amelia
    Efstathiou, Nikolaos
    Kholia, Krishna
    Rogers, Venessa
    Fallouh, Hazem
    Steyn, Richard
    Bishay, Ehab
    Kalkat, Maninder
    Naidu, Babu
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    Publication date
    2022-06-28
    Subject
    Nursing
    
    Metadata
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    Abstract
    Objectives: Malnutrition and weight loss are important risk factors for complications after lung surgery. However, it is uncertain whether modifying or optimising perioperative nutritional state with oral supplements results in a reduction in malnutrition, complications or quality of life. Design: A randomised, open label, controlled feasibility study was conducted to assess the feasibility of carrying out a large multicentre randomised trial of nutritional intervention. The intervention involved preoperative carbohydrate-loading drinks (4×200 mL evening before surgery and 2×200 mL the morning of surgery) and early postoperative nutritional protein supplement drinks two times per day for 14 days compared with the control group receiving an equivalent volume of water. Setting: Single adult thoracic centre in the UK. Participants: All adult patients admitted for major lung surgery. Patients were included if were able to take nutritional drinks prior to surgery and give written informed consent. Patients were excluded if they were likely unable to complete the study questionnaires, they had a body mass index <18.5 kg/m2, were receiving parenteral nutrition or known pregnancy. Results: All patients presenting for major lung surgery were screened over a 6-month period, with 163 patients screened, 99 excluded and 64 (41%) patients randomised. Feasibility criteria were met and the study completed recruitment 5 months ahead of target. The two groups were well balanced and tools used to measure outcomes were robust. Compliance with nutritional drinks was 97% preoperatively and 89% postoperatively; 89% of the questionnaires at 3 months were returned fully completed. The qualitative interviews demonstrated that the trial and the intervention were acceptable to patients. Patients felt the questionnaires captured their experience of recovery from surgery well. Conclusion: A large multicentre randomised controlled trial of nutritional intervention in major lung surgery is feasible and required to test clinical efficacy in improving outcomes after surgery. Trial registration number: ISRCTN16535341.
    Citation
    Kerr A, Lugg ST, Kadiri S, Swift A, Efstathiou N, Kholia K, Rogers V, Fallouh H, Steyn R, Bishay E, Kalkat M, Naidu B. Feasibility study of a randomised controlled trial of preoperative and postoperative nutritional supplementation in major lung surgery. BMJ Open. 2022 Jun 28;12(6):e057498. doi: 10.1136/bmjopen-2021-057498
    Type
    Article
    Handle
    http://hdl.handle.net/20.500.14200/4938
    Additional Links
    http://bmjopen.bmj.com/
    DOI
    10.1136/bmjopen-2021-057498
    PMID
    35768119
    Journal
    BMJ Open
    Publisher
    BMJ Publishing Group
    ae974a485f413a2113503eed53cd6c53
    10.1136/bmjopen-2021-057498
    Scopus Count
    Collections
    Thoracic Surgery

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