Operative versus non-operative treatment for 2-part proximal humerus fracture : a multicenter randomized controlled trial

RESEARCH ARTICLE Operative versus non-operative treatment for 2-part proximal humerus fracture: A multicenter randomized controlled trial Antti P. LaunonenID 1 *, Bakir O. SumreinID 1 , Aleksi ReitoID 2 , Vesa Lepola 1 , Juha PalonevaID 2 , Kenneth B. Jonsson 3 , Olof WolfID 3 , Peter Stro ¨m 3 , Hans E. BergID 4,5 , Li Fella ¨nder-Tsai 4,5 , Karl-Åke Jansson 4,5 , Daniel FellID 4,5 , Inger Mechlenburg 6,7 , Kaj DøssingID 8 , Helle ØstergaardID 8 , Aare Ma ¨rtsonID 9 , Minna K. LaitinenID 1 , Ville M. Mattila 1 , as the NITEP group 1Faculty of Medicine and Health Technology, University of Tampere and Tampere University Hospital, Tampere, Finland, 2Department of Orthopaedics, Central Finland Central Hospital, Jyva¨skyla¨, Finland, 3Department of Orthopaedics, Institute of Surgical Sciences, Uppsala University Hospital, Uppsala, Sweden, 4Division of Orthopedics and Biotechnology, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden, 5Department of Orthopedics, Karolinska University Hospital, Huddinge, Sweden, 6Department of Orthopaedic Surgery, Aarhus University Hospital, Aarhus, Denmark, 7Department of Clinical Medicine, Aarhus University, Aarhus, Denmark, 8Orthopedics Department, Viborg Regional Hospital, Viborg, Denmark, 9Department of Traumatology and Orthopedics, Tartu University Hospital and Tartu University, Tartu, Estonia *[email protected] Abstract Background Although increasingly used, the benefit of surgical treatment of displaced 2-part proximal humerus fractures has not been proven. This trial evaluates the clinical effectiveness of surgery with locking plate compared with non-operative treatment for these fractures. Methods and findings The NITEP group conducted a superiority, assessor-blinded, multicenter randomized trial in 6 hospitals in Finland, Estonia, Sweden, and Denmark. Eighty-eight patients aged 60 years or older with displaced (more than 1 cm or 45 degrees) 2-part surgical or anatomical neck proximal humerus fracture were randomly assigned in a 1:1 ratio to undergo either operative treatment with a locking plate or non-operative treatment. The mean age of patients was 72 years in the non-operative group and 73 years in the operative group, with a female sex distribution of 95% and 87%, respectively. Patients were recruited between February 2011 and April 2016. The primary outcome measure was Disabilities of Arm, Shoulder, and Hand (DASH) score at 2-year follow-up. Secondary outcomes included Constant–Murley score, the visual analogue scale for pain, the quality of life questionnaire 15D, EuroQol Group’s 5dimension self-reported questionnaire EQ-5D, the Oxford Shoulder Score, and complications. The mean DASH score (0 best, 100 worst) at 2 years was 18.5 points for the operative treatment group and 17.4 points for the non-operative group (mean difference 1.1 [95% CI −7.8 to 9.4], p = 0.81). At 2 years, there were no statistically or clinically significant betweenPLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 1 / 14 a1111111111 a1111111111 a1111111111 a1111111111 a1111111111 OPEN ACCESS Citation: Launonen AP, Sumrein BO, Reito A, Lepola V, Paloneva J, Jonsson KB, et al. (2019) Operative versus non-operative treatment for 2part proximal humerus fracture: A multicenter randomized controlled trial. PLoS Med 16(7): e1002855. https://doi.org/10.1371/journal. pmed.1002855 Academic Editor: Helen Handoll, Teesside University, UNITED KINGDOM Received: December 2, 2018 Accepted: June 19, 2019 Published: July 18, 2019 Copyright: ©2019 Launonen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Data Availability Statement: Study data cannot be shared publicly because of confidentiality requirements under Swedish and Finnish law. Deidentified patient data are available from the NITEP group and from Tampere University Hospital (contact via http://nitep.eu/en/contact/ or www.pshp.fi,heli.pehrm[email protected]) for researchers who meet the criteria for access to confidential data. group differences in any of the outcome measures. All 3 complications resulting in secondary surgery occurred in the operative group. The lack of blinding in patient-reported outcome assessment is a limitation of the study. Our assessor physiotherapists were, however, blinded. Conclusions This trial found no significant difference in clinical outcomes at 2 years between surgery and non-operative treatment in patients 60 years of age or older with displaced 2-part fractures of the proximal humerus. These results suggest that the current practice of performing surgery on the majority of displaced proximal 2-part fractures of the humerus in older adults may not be beneficial. Trial registration ClinicalTrials.gov NCT01246167. Author summary Why was this study done? • Proximal humerus fractures (PHFs) are among the most common fractures in older adults. The risks for suffering a PHF increase with age, especially after the age of 60 years. • Non-operative treatment of non-displaced PHF is uniformly approved, but the treatment of displaced 2-part PHF remains controversial. Recently, several studies have reported a significant increase in the surgical treatment of 2-part PHF, mainly due to the introduction of locking plates suitable for treating osteoporotic bone. • In this study, we investigated whether surgery with a locking plate is superior to nonoperative treatment with a collar-cuff and early physiotherapy in the treatment of 2-part PHF involving the surgical neck. What did the researchers do and find? • We randomly allocated 88 patients aged 60 years or older with displaced 2-part PHF into 2 groups. One group underwent surgery with a locking plate and the other conservative (non-operative) treatment. • We recorded the Disabilities of Arm, Shoulder, and Hand (DASH) score, other measures of shoulder function and quality of life, and complications at 2-year follow-up. • We found no significant or clinically important between-group differences in all outcomes. A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 2 / 14 Funding: This research study received a grant from the Academy of Finland (www.aka.fi; ref 275481, ML) for the Finland branch of the consortium and the overall maintenance of the trial. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Competing interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: OW declared a consultancy for Anatomica, and a paid presentation for DePuy Synthes and Link Sweden. AR declared a paid lecture (Orion Ltd.). The other authors have declared that no competing interests exist. Abbreviations: AE, adverse event; CS, Constant– Murley score; DASH, Disabilities of Arm, Shoulder, and Hand; MCID, minimal clinically important difference; OSS, Oxford Shoulder Score; PHF, proximal humerus fracture; PROM, patientreported outcome measure; SAE, serious adverse event; VAS, visual analogue scale for pain. What do these finding mean? • This trial provides no evidence that surgery is superior to non-operative treatment in the treatment of displaced 2-part PHF involving the surgical neck in older adults. • These results suggest that the current practice of performing surgery on the majority of displaced 2-part proximal fractures of the humerus in older adults may not be beneficial. Introduction Proximal humerus fractures (PHFs) are among the most common fractures in the older adult population [1,2]. In a Swedish nationwide study, the person-based incidence of PHF in adults was 175 per 100,000 person-years in women and 68 per 100,000 person-years in men [3]. The risk for having a PHF increases with age, especially after the age of 60 years [3,4]. The majority of PHFs are associated with a low-energy fall [4]. According to the published literature, minimally displaced or 2-part fractures constitute between 77% and 84% of all fractures [2,5]. Additionally, in another study, 76% are classified as AO Foundation/Orthopaedic Trauma Association (AO/OTA) A-class fractures [6], for which non-operative treatment can be considered. Fracture comminution and displacement, especially in 3and 4-part fractures, on the other hand, are considered to be potential indications for operative treatment [7]. Recently, several studies have reported a substantial increase in surgery and claim it has now become current practice in the treatment of PHF, especially among the people aged over 60 years [3,8]. This increase has been mainly due to the introduction of locking plates, even though proper evidence of the superiority of surgery is lacking [8]. A few randomized controlled trials have compared operative treatment (plating or hemi-endoprosthesis) with nonoperative treatment in displaced 3and 4-part fractures [9–12]. The PROFHER trial, in which the majority of the fractures were displaced according to Neer criteria, also included 2-part fractures [12]. The study showed no differences between operative treatment and non-operative treatment based on a patient-reported outcome measure (PROM) or quality of life score. Based on the most recent Cochrane review as well as on other meta-analyses, no statistically or clinically significant difference in PROMs between operative and non-operative treatment has been observed [13–15]. It could be hypothesized that patients with displaced (defined by Neer criteria as more than 1 cm or 45 degrees) 2-part fractures [16] would benefit from operative treatment with a locking plate, but there is a scarcity of knowledge of the treatment outcomes associated with displaced 2-part fractures. We therefore conducted a multicenter, randomized, controlled efficacy trial that compared operative treatment with a locking plate with non-operative treatment in patients aged 60 years or over with 2-part displaced PHFs [17]. Methods Study design This PHF trial was a superiority, multicenter NITEP (Nordic Innovative Trial to Evaluate osteoPorotic fractures) group trial. The trial was conducted at 6 hospitals in 4 Northern European countries (Finland, Sweden, Denmark, and Estonia) [17]. All collaborating hospitals are A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 3 / 14 emergency hospitals that routinely treat trauma patients. A specialized upper extremity team at each participating hospital provided the allocated treatment for the randomized patients, who were recruited between February 2011 and April 2016. The patients were informed about the treatment options during a pre-interviewing session, and all eligible patients gave their written informed consent before the randomization and initialization of the allocated treatment. The trial protocol was approved by the Regional Ethics Committee of Tampere University Hospital. In addition, the ethical committees of all participating hospital districts granted their ethical approval, and each hospital provided trial authorization before starting recruitment. Furthermore, independent steering and monitoring committees inspected the trial. The trial was designed by members of the protocol committee, and details of the trial design and methods have been published elsewhere [17]. In the protocol [17], 2 trial strata were described. Stratum I comprised 2-part fractures and stratum II comprised 3and 4-part fractures. It was foreseen in the original protocol that stratum I would commence first, and therefore the reporting was planned separately for each protocol. At present, stratum II is still in the recruitment phase (159 of 218 patients recruited by 2 April 2019), which is scheduled to be completed during 2019. The analysis and reporting of these patients will start after the 2-year follow-up period. The trial protocol was signed by the principal investigator at each participating hospital in order to respect the approved treatment strategies. The protocol was held in an Investigator Site File (ISF), and good clinical practice was the guiding principal in maintaining the study. The local investigators and the trial manager gathered the data. We used a prospective, randomized, open-label, blinded-endpoint design, where patients knew their allocation, but the persons who collected and analyzed the data and the authors were unaware of the study-group allocation of the patients. The authors vouch for the accuracy and completeness of the reported data and analyses, and the fidelity of the study to the protocol. The authors wrote the manuscript and made the decision to submit the manuscript for publication. This study is reported as per the Consolidated Standards of Reporting Trials (CONSORT) guideline (S1 CONSORT Checklist). Patients Patients aged 60 years or over with displaced 2-part low-energy PHF (in which the fracture line emerges through the surgical or anatomical neck) occurring less than 2 weeks before allocation and treatment onset were eligible for inclusion. Displacement was defined by Neer classification (displacement more than 1 cm or 45 degrees, with bony contact) [16]. Pre-allocation radiograph along with computed tomography (CT) confirmed the classification. Furthermore, 2 upper extremity trauma surgeons reviewed each patient before randomization to confirm the classification. Detailed inclusion and exclusion criteria are presented in S1 Appendix. Randomization and blinding Randomization was performed at the patient level. Eligible patients were randomly assigned in a 1:1 ratio to undergo operative treatment with a locking plate or non-operative treatment. After enrollment, patients underwent randomization by means of a telephone call from the treating surgeon to the coordinating center’s research nurse. Sealed envelopes were used, and the pre-trial randomization sequence was generated with 10 blocks according to center and stratified by age (60 to 70 years, more than 70 years) due to the association between age and the measured outcomes. The trial was semi-blinded, and the outcome assessors—trained physiotherapists who otherwise did not take part in the study—were unaware of which treatment group patients belonged to, and patients were encouraged not to reveal their treatment group. In addition, patients wore a T-shirt to cover any scars on their shoulder. A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 4 / 14 Surgical and postoperative procedures The treatments in the operative and non-operative groups were standardized [17]. Patients who received operative treatment with a Philos locking plate (Synthes, Solothurn, Switzerland) were operated on by an upper extremity trauma surgeon. The operating surgeon had a minimum of 5 years’ experience in shoulder trauma, and thus any learning curve problems in the treatment were avoided. After treatment, both groups received the same physiotherapy described in more detail in S2 Appendix. A collar-cuff or sling was worn for 3 weeks to reduce pain, and pendulum movements were initiated from the first day possible (non-operative patients immediately and surgery patients from first post-op day). Elbow, wrist, and fingers were mobilized, and the use of the injured upper extremity in daily activities was encouraged. After 3 weeks, active range-of-motion exercises were initiated under the supervision of a physiotherapist. Both groups were offered supervised physiotherapy rehabilitation sessions. At the follow-up visits, the patients were asked about the number of sessions received. Outcome measures The primary outcome was Disabilities of the Arm, Shoulder, and Hand (DASH) score measured at 2-year follow-up. The DASH is a PROM with 36 questions on coping in different everyday-life tasks [18]. The scale ranges from 0 to 100, with a low number indicating better function. The minimal clinically important difference (MCID) on the DASH has been estimated to be 10 to 15 [19–21]. Secondary outcomes included Constant–Murley score (CS) [22], the visual analogue scale for pain (VAS; 0 to 100 mm) [23], the quality of life questionnaire 15D [24], the EuroQol Group’s 5-dimension self-reported questionnaire EQ-5D(-3L) (with normal values from Finland) [25], and the Oxford Shoulder Score (OSS) [26]. The CS has a known wide interobserver variation, and therefore we arranged pre-trial training for the investigators in order to harmonize the measurements. The follow-up questionnaires included a separate section on adverse events (AEs), defined as untoward medical occurrences that may or may not have a causal relationship with the treatment administered. AEs were classified as serious AEs (SAEs) if they necessitated hospitalization or prolonged inpatient hospital care, or if they were life-threatening or resulted in death. Complications were also recorded (infection, nerve damage, bleeding, malor non-union, hardware problems). The data were collected during the research visits at 3 months, 6 months, 12 months, and 24 months. The baseline and follow-up data acquired from the patients were stored in paper portfolios that were analyzed after the last patient’s 2-year follow-up visit in April 2018. The portfolios included the patients’ baseline characteristics, patient questionnaires, validated questionnaires, and case report files that contained information about allocation group, crossovers (treatment another than the randomized allocation), AEs, and SAEs. Ethical approval Primary approval was received from the Regional Ethics Committee of Tampere University Hospital, ETL-code R10127. Participation was voluntary. All data are anonymous. Statistical analysis The trial was powered to detect a MCID in the DASH score of at least 10 points with a standard deviation (SD) of 15 (effect size d= 0.67) points. The initial planned sample size was 74 patients, which, at a 5% significance level, would provide 80% power to detect an effect size of 0.67 for the comparison of the 2 different treatment methods. Because the anticipated loss to follow-up was higher than the originally expected 10%, it was decided to raise the number of A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 5 / 14 recruited patients from 81 to 88, resulting in 44 patients per group. This and other changes to protocol are summarized in S3 Appendix. The baseline characteristics were analyzed with descriptive statistics. Although we stated in the original trial protocol published in 2012 that subgroup analysis with respect to smoking, fracture type, and other diseases would be carried out, this was not done due to the rarity of these baseline characteristics in our sample. For the primary analysis, the primary and secondary outcomes at 2 years were compared between study groups with 95% confidence intervals. The principal analysis of the trial was performed after all participants had completed the 2-year follow-up. Trial analyses were conducted according to a prespecified statistical plan with the use of R software, version 3.5. All analyses were on an intention-to-treat basis and included all randomized patients in the groups to which they were randomized. Six patients were lost immediately after the allocation or were missing data from all the time points, and these patients were excluded from all the analyses. For the remaining patients, each outcome was treated as a time series in the individual patients, and the methods of linear interpolation and last observation carried forward were used to impute the missing data. A per protocol analysis was also conducted as a sensitivity analysis for the primary outcome. Continuous outcomes were compared using the Student t test. For each comparison, the homogeneity of variance was tested using Levene’s test meeting the assumption of the Student ttest. Due to the skewness of the PROMs, we also used Mann– Whitney U test to compare the ranks between groups. All appropriate statistical tests were 2-sided. Before revealing the randomization code, the writing committee (APL, VMM, MKL, and BOS) developed and recorded 2 interpretations of the results based on a blinded review of the primary outcome data (treatment A compared with treatment B). Thus, we aimed to decrease the possible researcher bias when interpreting the results. Only after the members of the writing committee had agreed that there would be no further changes in the interpretations, and unanimous consensus over the analysis reached, was the randomization code revealed, the correct interpretation chosen, and the manuscript finalized. Patient and public involvement There was no patient involvement during the designing, recruiting, or conducting of the trial. However, after publication and dissemination of the results, patient organizations, health policy makers, and the general public will be informed of the important findings of the trial by means of congresses, social media, and general newsfeeds. Results Between February 2011 and April 2016, a total of 88 patients with PHF with surgical neck involvement were randomly assigned to undergo either operative treatment with a locking plate or non-operative treatment. In total, 44 patients were assigned to undergo operative treatment with a locking plate and 44 to non-operative treatment (Fig 1). The characteristics of the study population at the time of enrollment are shown in Table 1. Primary outcome measure The mean DASH score at 2 years was 18.5 (SE 3.1) points for the operative treatment group and 17.4 (SE 2.8) points for the non-operative group. The between-group difference was 1.1 points (95% CI −7.8 to 9.4, p = 0.81). Detailed results are shown in Fig 2 and Table 2. At 2 years, there were no statistical or clinically significant between-group differences in the study groups. Sensitivity analysis using the available data showed similar results (S4 Appendix). A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 6 / 14 Fig 1. Participant flow diagram of the NITEP study. https://doi.org/10.1371/journal.pmed.1002855.g001 A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 7 / 14 When stratified by age, the between-group difference in mean DASH score (with ttest) at 2 years in patients aged 60–70 years was −0.2 (95% CI −10.1 to 9.7, p = 0.97). The between-group difference in mean DASH score at 2 years in patients aged more than 70 years was 1.7 (95 CI −11.2 to 14.5, p = 0.79). An additional secondary sensitivity analysis, requested by an external reviewer, showed no significant between-group difference in the number of patients with a DASH score difference of 10 points or more between baseline and 24 months (p = 0.30); see S4 Appendix. Secondary outcomes At 2 years, we found no statistical or clinically significant between-group differences in study groups for the CS (mean 68.0 points [SE 3.2] in the operative treatment group compared with 66.0 points [SE 3.3] in the non-operative group; between-group difference 2.0 [95% CI −5.6 to 9.6], p = 0.6). For the OSS, the mean was 40.2 points (SE 1.5) in the operative treatment group compared with 41.5 points (SE 1.4) in the non-operative group (between-group difference −1.3 [95% CI −5.3 to 2.8], p = 0.54). For the EQ-5D, the mean was 0.87 points (SE 0.02) in the operative treatment groups compared with 0.89 points (SE 0.02) in the non-operative group (betweengroup difference −0.02 [95% CI −0.08 to 0.02], p = 0.27). For the VAS, the mean was 11.5 points (SE 3.3) in the operative treatment group compared with 9.9 points (SE 2.7) in the non-operative group (between-group difference 1.6 [95% CI −6.8 to 9.9], p = 0.72). For the 15D, the mean was 0.862 points (SE 0.029) in the operative treatment groups compared with 0.879 points (SE 0.017) in the non-operative group (between-group difference −0.016 [95% CI −0.084 to 0.049], p = 0.6). For physiotherapy, the median number of visits was 4 in the operative group (range 0 to 25 visits) compared with 4 in the non-operative group (range 0 to 28 visits) (p = 0.38). Complications At 2 years, there were 3 complications. They all occurred in the operative group and required subsequent surgery. No other complications were detected. One patient fell and sustained a Table 1. Characteristics of 88 patients with a displaced 2-part proximal humerus fracture at baseline. Patient characteristic Surgical group n = 44 Non-operative group n = 44 Mean age (SD, range) 72 (7.4, 60–90) 73 (7.7, 60–86) Age group 60–69 years 17 20 70 years or above 27 24 Female sex 41 (95%) 39 (87%) Fracture type: Surgical neck 44 (100%) 44 (100%) Fracture on dominant side 15 (35%) 16 (36%) Smoking 3 7 Diabetes 9 7 Neurological diseases 1 2 Mean DASH score (SD)�17.1 (20.0) 15.9 (19.8) Mean OSS (SD)�41.7 (11.1) 40.5 (11.2) Mean EQ-5D score (SD)�0.87 (0.12) 0.85 (0.12) Mean 15D score (SD)�0.888 (0.087) 0.883 (0.090) Data are number (percent) unless otherwise indicated. �Baseline values measured before the fracture. DASH, Disabilities of Arm, Shoulder, and Hand; OSS, Oxford Shoulder Score. https://doi.org/10.1371/journal.pmed.1002855.t001 A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 8 / 14 peri-implant fracture distal to the tip of the plate. This fracture was treated with open reduction and internal fixation by long anatomical locking plate. Two patients had implant failures because proximal screws migrated into the joint. These patients were treated with revision operation, and the screws were changed. The mean time to revision operation was 5.5 months (range 1.3 to 12.4 months). In the non-operative group, there were no complications; however, the difference between the groups was not statistically significant (3 versus 0, p = 0.24). One patient died during the study period. The death was not related to the trial. No patient withdrew from the study because of adverse effects. Fig 2. Between-group differences in mean DASH score (0 best, 100 worst) from baseline to 24 months. Vertical lines represent 95% confidence intervals. DASH, Disabilities of Arm, Shoulder, and Hand. https://doi.org/10.1371/journal.pmed.1002855.g002 A randomised trial of operative versus non-operative treatment for two-part proximal humerus fracture PLOS Medicine | https://doi.org/10.1371/journal.pmed.1002855 July 18, 2019 9 / 14