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Nordic Innovative Trials to Evaluate osteoPorotic Fractures (NITEP) Collaboration: The Nordic DeltaCon Trial protocol-non-operative treatment versus reversed total shoulder arthroplasty in patients 65 years of age and older with a displaced proximal humerus fracture: a prospective, randomised controlled trial

Launonen, AP (författare)
Tampere Univ Hosp, Tampere, Finland
Fjalestad, T (författare)
Oslo Univ Hosp, Oslo, Norway
Laitinen, MK (författare)
Tampere Univ Hosp, Tampere, Finland
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Lahdeoja, T (författare)
Helsinki Univ Hosp, Helsinki, Finland
Ekholm, C (författare)
Sahlgrens Univ Hosp, Gothenburg, Sweden
Wagle, T (författare)
Oslo Univ Hosp, Oslo, Norway
Mattila, VM (författare)
Tampere Univ Hosp, Tampere, Finland
Sumrein, BO (författare)
Tampere Univ Hosp, Tampere, Finland
Paloneva, J (författare)
Jyvaskyla Cent Hosp, Jyvaskyla, Finland
Lehtimaki, K (författare)
Turku Univ Hosp, Turku, Finland
Thillemann, T (författare)
Aarhus Univ Hosp, Aarhus, Denmark
Berg, H (författare)
Karolinska Institutet,Karolinska Univ Hosp, Stockholm, Sweden
Wolf, Olof (författare)
Uppsala universitet,Ortopedi
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 (creator_code:org_t)
2019-01-29
2019
Engelska.
Ingår i: BMJ open. - : BMJ. - 2044-6055. ; 9:1, s. e024916-
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The proximal humerus fracture (PHF) is one of the most common fractures in the elderly. The majority of PHFs are treated non-operatively, while 15%–33% of patients undergo surgical treatment. Recent randomised controlled trial (RCT) and meta-analyses have shown that there is no difference in outcome between non-operative treatment and locking plate or hemi-arthroplasty. During the past decade, reverse total shoulder arthroplasty (RTSA) has gained popularity in the treatment of PHF, although there is a lack of RCTs comparing RTSA to non-operative treatment.MethodsThis is a prospective, single-blinded, randomised, controlled, multicentre and multinational trial comparing RTSA with non-operative treatment in displaced proximal humeral fractures in patients 65–85 years. The primary outcome in this study is QuickDASH-score measured at 2 years. Secondary outcomes include visual analogue scale for pain, grip strength, Oxford shoulder score, Constant score and the number of reoperations and complications.The hypothesis of the trial is that operative treatment with RTSA produces better outcome after 2 and 5 years measured with QuickDASH.Ethics and disseminationIn this protocol, we describe the design, method and management of the Nordic DeltaCon trial. The ethical approval for the trial has been given by the Regional Committee for Medical and Health Research Ethics, Norway. There have been several examples in orthopaedics of innovations that result in failure after medium-term follow-ups . In order to prevent such failures and to increase our knowledge of RSTA, we feel a large-scale study of the effects of the surgery on the outcome that focuses on the complications and reoperations is warranted. After the trial 2-year follow-up, the results will be disseminated in a major orthopaedic publication.Trial registration numberNCT03531463; Pre-Results.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Ortopedi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Orthopaedics (hsv//eng)

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