Hip fracture patients often have an impaired nutritional status at the time of fracture, which can result in a higher complication rate, prolonged rehabilitation time and increased mortality. A study was designed to evaluate the effect of nutritional intervention on nutritional status, functional status, total length of stay, postoperative complications and cost-effectiveness.
Open-labelled, multi-centre, randomized controlled trial in hip fracture patients aged 55 years and above. The intervention group receives dietetic counselling (by regular home visits and telephone calls) and oral nutritional supplementation for three months after surgery. The control group receives usual dietetic care as provided by the hospital. Outcome assessment is performed at three and six months after hip fracture.
Patient recruitment has started in July 2007 and has ended in December 2009. First results are expected in 2011.
In the elderly, the incidence of hip fractures is high and it will increase in the nearby future due to the changes in the age demographics, the increased life expectancy and the continuous improvement of health care [1, 2]. Hip fractures are one of the most common reasons for hospital admission and transfers to nursing home . Only 37% of the hip fracture patients will return to their pre-fracture functional status, leading to high health care costs and a major burden on health care utilization. These costs are not only determined by acute hospital costs, but even more by the long term costs such as recovery in rehabilitation clinics, the need for home care and the increased burden on informal care givers [4, 5].
At the time of hospitalization for a hip fracture, the prevalence of malnutrition ranges from 2%  to 63% . Poor nutritional status in hip fracture patients is associated with impaired muscle function, disability , loss of independency, lower mental function, decreased quality of life , delayed wound healing, higher complication rate [9, 10], prolonged rehabilitation time [8, 9, 11] and increased mortality both during and after hospital admission [9, 12–16]. During hospital admission, the nutritional status can deteriorate further due to increased energy expenditure caused by metabolic stress, combined with a low intake due to the lack of appetite, nausea and psychological factors.
In the past decades, several studies have been conducted to determine the effectiveness of various types of nutritional intervention in elderly hip fracture patients on the length of stay, mortality, complications, nutritional and functional status. Results of these studies are inconsistent and the evidence for nutritional supplementation remains limited . Oral nutritional supplementation is the simplest type of nutritional intervention for hip fracture patients to improve the energy and protein intake and nutritional status, although compliance is often poor . Personal attention from a dietetic assistant can improve compliance with and tolerance of nutritional supplements  and help to establish a prolonged effect of the nutritional intervention.
The aim of the present study is to investigate the effect of intensive dietary intervention, comprising a combination of dietetic counselling and oral nutritional supplementation during hospitalization and after discharge, on the nutritional status, total length of stay and health care costs after hip fracture. We hypothesize that the combination of dietetic counselling and oral nutritional supplementation in hip fracture patients will improve patients' energy and protein intake, improve their nutritional status, reduce the number of complications and total length of stay in hospital and rehabilitation clinics, and lower health care costs.
Study design, general outline and randomization
Figure 1 shows the design of the study, which is an open-label, randomized controlled, multi-centre trial. Patient allocation to intervention or control group is performed after stratification for hospital, gender, and age (55-74 years vs. 75 years and above). Patients allocated to the intervention group receive dietetic counselling and oral nutritional supplementation for 3 months following surgery. The control group receives usual nutritional care. Patients are enrolled within 5 days after surgical treatment of hip fracture, and baseline measurements are performed immediately after enrolment. Outcome measurements are performed at the patient's home at three and six months following hip fracture. The study has been approved by the Medical Ethical Committee of Maastricht University Medical Centre and Maastricht University and is conducted according to the Declaration of Helsinki.
Study population and recruitment of the study population
For patient recruitment, a daily inventory is made of hip fracture patients admitted to the surgical and orthopaedic wards of three hospitals in South-Limburg in The Netherlands: Maastricht University Medical Centre, Maastricht (MUMC); Atrium Medical Centre, Heerlen (AMC); and Orbis Medical Centre, Sittard (OMC). Based on this inventory, eligible candidates are invited to participate and written informed consent is obtained within 5 days after surgery. Inclusion criteria are aged 55 years and above and hospital admission for surgical treatment of hip fracture. Patients are excluded if they have a pathological or periprosthetic fracture; disease of the bone metabolism (e.g. M Paget, M Kahler, hyperparathyroidism); life expectancy of less than 1 year due to underlying disease (e.g. cancer); use oral nutritional supplements before hospital admission; are unable to speak Dutch; live outside the region of South-Limburg, or are bedridden before the hip fracture. Patients who suffer from dementia or who are cognitively impaired according to the Abbreviated Mental Test (AMT) (a score of less than 7) are also excluded [20, 21].
The nutritional intervention is a combination of dietetic counselling and oral nutritional supplements for three months. The intervention starts during hospital admission and continues after discharge during the stay at the rehabilitation clinic or at the patient's home. During hospitalization, the study dietician visits the patient twice. At the first visit, two to five days after surgery and immediately after baseline measurements, the dietician interviews the patient regarding medical and social status, and pre-fracture mobility. The dietician also performs a 24-hour recall and takes a general dietary history of the patients' diet before hospitalization. Next, the patient receives the nutritional supplement, a milk-based supplement providing 21 kJ (500 kcal) and 40 g of protein. The dietician advices the patient on the consumption of the supplement and arranges extra care or services to optimize the food intake if necessary. Before hospital discharge, the dietician visits the patient for the second time. During this visit, a 24-hour recall is performed and the consumption of the nutritional supplement is evaluated. Furthermore, arrangements are made to continue the dietetic advice and the consumption of the nutritional supplement at home or during the stay at the rehabilitation clinic. At home or during the stay in a rehabilitation clinic, the dietician visits the patient three times (one week, two weeks and six weeks after discharge) and makes five telephone calls with the patient (three, four, five, eight and ten weeks after discharge). During these visits, food intake and supplement use is assessed by a 24-hour dietary recall, and tailor-made dietetic advice is given to optimize the amount and composition of the diet. As soon as the patient meets nutritional requirements with a normal diet, the use of the nutritional supplement is stopped. Compliance with the nutritional supplement is evaluated by the 24-hour dietary recalls, patients' registration of the consumption in a diary and by collecting the capsules of the cans of the nutritional supplement during the home visits.
Patients allocated to the control group receive usual care as provided in the hospital, rehabilitation clinic or at home, i.e. dietetic care or nutritional supplements are only provided on demand of the medical doctor in charge.
The primary outcome measure is total length of stay in hospital and rehabilitation clinics including hospital readmissions. Secondary outcome measures, assessed at three and six months after hip fracture, are nutritional status, functional status, quality of life, complication rate and one-year mortality.
Assessment of nutritional status includes total food and supplement intake, measurement of body composition, muscle strength and biochemical parameters in blood. Anthropometric measurements are body weight, height, thickness of biceps, triceps, sub scapula and supra-iliac skin fold, and circumference of mid-arm, waist and hip. Body composition is measured by bio-electrical impedance spectroscopy. Biochemical parameters include albumin, pre-albumin, CRP, haemoglobin and hematocrit in blood.
Functional status is measured by the Groningen Activity Restriction Scale (GARS) , which assesses disability with regard to (instrumental) activities of daily living, and by the Harris Hip Score to evaluate changes in hip function.
Quality of life is measured using the EuroQoL [23, 24] and the Medical Outcomes Study 36-item Short-Form Health Survey [25, 26]. Mental state and depression is assessed by the Mini-Mental State Examination (MMSE) and the Hospital Anxiety and Depression Scale (HADS) [27, 28]. To measure fatigue, the Checklist Individual Strength (CIS)  is used.
Pre-fracture information on co-morbidity, medication use and fracture history is obtained by interviewing the patient. Information on type of hip fracture, surgical treatment, admission and discharge dates, and post-operative complications are obtained from medical charts.
The costs analysis will compare the costs of the nutritional intervention and the usual care over a 6-month period . Medical and non-medical costs are obtained from a 3-month retrospective standardized costing questionnaire. Health care costs will be estimated according to the Dutch guideline for cots-analysis in health care research . Incremental costs between the strategies will be related to a difference in outcome during 6 months follow up and being expressed in a incremental cost-effectiveness ratio. Statistical uncertainty will be assessed using bootstrap simulations .
A process evaluation is carried out to evaluate whether the nutritional intervention follows the protocol, with regard to the dietetic counselling and the consumption of the nutritional supplement. The feasibility of the nutritional intervention program is evaluated through summative evaluation with the identified stakeholders being patients and health care providers (medical doctors, dieticians, nurses). Experiences and opinions on feasibility, barriers and stimulating or facilitating factors for implementing the nutritional intervention in the transmural care are identified from the stakeholders' perspective. Data are collected by structured interviews with patients and in-depth interviews in a representation of patients and health care providers. A subsample of health care providers is asked to participate in a focus group meeting. The results of the process evaluation will be used as a basis for successful implementation of the nutritional intervention program in the transmural care for hip fracture patients.
Sample size/power calculation
Nutritional intervention in hip fracture patients can result in an estimated reduction in total length of hospital and rehabilitation stay by 31.3% (SD: 59.0%). A sample of 75 patients per treatment arm is sufficient to detect this effect with a power of 90% and a two tailed alpha of 0.05. To detect a between-group difference in weight of 2.13 kg (SD: 3.72 kg), a number of 61 patients per treatment arm is sufficient using the same power and alpha.
The intervention effects of primary and secondary outcome measures will be analyzed according to the intention-to-treat principle. In addition, a secondary per protocol analysis will be performed in patients with adequate compliance. After initial univariate analyses of differences in the primary outcome between the intervention and control group, multivariate analyses will be used to adjust for potential confounders such as age, gender, baseline values of nutritional status, physical disability, co-morbidity, and mental state including depression.
Patient recruitment has started in July 2007 and has ended in December 2009. Follow-up of the patients is to be completed in June 2010, except for data of one-year mortality. First results are expected in 2011. We expect that this study will answer the question whether nutritional intervention in hip fracture patients improves their nutritional and functional status, resulting in a shorter length of stay in hospital and rehabilitation clinics, fewer postoperative complications, lower mortality, and cost-effectiveness.
This study was funded by the Netherlands Organization for Health Research and Development (ZonMw 80-007022-98-07510). The authors like to thank Angela Hendrikx and Marionne Vaessen for valuable assistance in data acquisition. We are also grateful to the dieticians, nurses, trauma surgeons, orthopaedic surgeons and other staff members from the participating clinical centres: Maastricht University Medical Centre, Maastricht, Atrium Medical Centre, Heerlen, and Orbis Medical Centre, Sittard, for their continuous support.
Department of Epidemiology, Maastricht University Medical Centre
Department of Dietetics, Maastricht University Medical Centre
Department of Trauma surgery, Maastricht University Medical Centre
Department of Orthopaedic Surgery, Maastricht University Medical Centre
Department of Health Organization, Policy and Economics, Maastricht University Medical Centre, and Institute of Health Policy and Management, Erasmus University Rotterdam
Department of Orthopaedic Surgery, Orbis Medical Centre
Department of Surgery, Atrium Medical Centre
Barrett-Connor E: The economic and human costs of osteoporotic fracture.Am J Med 1995,98(2A):3S-8S.PubMedView Article
De Laet CE, Pols HA: Fractures in the elderly: epidemiology and demography.Baillieres Best Pract Res Clin Endocrinol Metab 2000,14(2):171–179.PubMedView Article
Cummings SR: Treatable and untreatable risk factors for hip fracture.Bone 1996,18(3 Suppl):165S-167S.PubMedView Article
Haentjens P, Autier P, Barette M, Boonen S: Costs of care after hospital discharge among women with a femoral neck fracture.Clin Orthop Relat Res 2003, (414):250–258.
Nurmi I, Narinen A, Luthje P, Tanninen S: Cost analysis of hip fracture treatment among the elderly for the public health services: a 1-year prospective study in 106 consecutive patients.Arch Orthop Trauma Surg 2003,123(10):551–554.PubMedView Article
Maffulli N, Dougall TW, Brown MT, Golden MH: Nutritional differences in patients with proximal femoral fractures.Age Ageing 1999,28(5):458–462.PubMedView Article
Murphy MC, Brooks CN, New SA, Lumbers ML: The use of the Mini-Nutritional Assessment (MNA) tool in elderly orthopaedic patients.Eur J Clin Nutr 2000,54(7):555–562.PubMedView Article
Lumbers M, Driver LT, Howland RJ, Older MW, Williams CM: Nutritional status and clinical outcome in elderly female surgical orthopaedic patients.Clin Nutr 1996,15(3):101–107.PubMedView Article
Paillaud E, Bories PN, Le Parco JC, Campillo B: Nutritional status and energy expenditure in elderly patients with recent hip fracture during a 2-month follow-up.Br J Nutr 2000,83(2):97–103.PubMed
Patterson BM, Cornell CN, Carbone B, Levine B, Chapman D: Protein depletion and metabolic stress in elderly patients who have a fracture of the hip.J Bone Joint Surg Am 1992,74(2):251–260.PubMed
Bastow MD, Rawlings J, Allison SP: Undernutrition, hypothermia, and injury in elderly women with fractured femur: An injury response to altered metabolism?The Lancet 1983,321(8317):143–146.View Article
Bachrach-Lindstrom M, Johansson T, Unosson M, Ek AC, Wahlstrom O: Nutritional status and functional capacity after femoral neck fractures: a prospective randomized one-year follow-up study.Aging (Milano) 2000,12(5):366–374.
Bastow MD, Rawlings J, Allison SP: Benefits of supplementary tube feeding after fractured neck of femur: a randomised controlled trial.Br Med J (Clin Res Ed) 1983,287(6405):1589–1592.View Article
Hedstrom M: Hip fracture patients, a group of frail elderly people with low bone mineral density, muscle mass and IGF-I levels.Acta Physiol Scand 1999,167(4):347–350.PubMedView Article
Jallut D, Tappy L, Kohut M, Bloesch D, Munger R, Schutz Y, Chiolero R, Felber JP, Livio JJ, Jequier E: Energy balance in elderly patients after surgery for a femoral neck fracture.JPEN 1990,14(6):563–568.
Lumbers M, New SA, Gibson S, Murphy MC: Nutritional status in elderly female hip fracture patients: comparison with an age-matched home living group attending day centres.Br J Nutr 2001,85(6):733–740.PubMedView Article
Avenell A, Handoll HH: Nutritional supplementation for hip fracture aftercare in older people.Cochrane Database Syst Rev 2006, (4):CD001880.
Bruce D, Laurance I, McGuiness M, Ridley M, Goldswain P: Nutritional supplements after hip fracture: poor compliance limits effectiveness.Clin Nutr 2003,22(5):497–500.PubMedView Article
Duncan DG, Beck SJ, Hood K, Johansen A: Using dietetic assistants to improve the outcome of hip fracture: a randomised controlled trial of nutritional support in an acute trauma ward.Age Ageing 2006,35(2):148–153.PubMedView Article
Swain DG, Nightingale PG: Evaluation of a shortened version of the Abbreviated Mental Test in a series of elderly patients.Clin Rehabil 1997,11(3):243–248.PubMedView Article
Swain DG, O'Brien AG, Nightingale PG: Cognitive assessment in elderly patients admitted to hospital: the relationship between the shortened version of the Abbreviated Mental Test and the Abbreviated Mental Test and Mini-Mental State Examination.Clin Rehabil 2000,14(6):608–610.PubMedView Article
Kempen GI, Miedema I, Ormel J, Molenaar W: The assessment of disability with the Groningen Activity Restriction Scale. Conceptual framework and psychometric properties.Soc Sci and Med 1996,43(11):1601–1610.View Article
Tidermark J, Bergstrom G, Svensson O, Tornkvist H, Ponzer S: Responsiveness of the EuroQol (EQ 5-D) and the SF-36 in elderly patients with displaced femoral neck fractures.Qual Life Res 2003,12(8):1069–1079.PubMedView Article
Tidermark J, Zethraeus N, Svensson O, Tornkvist H, Ponzer S: Femoral neck fractures in the elderly: functional outcome and quality of life according to EuroQol.Qual Life Res 2002,11(5):473–481.PubMedView Article
Aaronson NK, Muller M, Cohen PD, Essink-Bot ML, Fekkes M, Sanderman R, Sprangers MA, te Velde A, Verrips E: Translation, validation, and norming of the Dutch language version of the SF-36 Health Survey in community and chronic disease populations.J Clin Epidemiol 1998,51(11):1055–1068.PubMedView Article
Ware JE Jr, Sherbourne CD: The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection.Med Care 1992,30(6):473–483.PubMedView Article
Scaf-Klomp W, Sanderman R, Ormel J, Kempen GI: Depression in older people after fall-related injuries: a prospective study.Age Ageing 2003,32(1):88–94.PubMedView Article
Zigmond AS, Snaith RP: The hospital anxiety and depression scale.Acta Psychiatr Scand 1983,67(6):361–370.PubMedView Article
Beurskens AJ, Bultmann U, Kant I, Vercoulen JH, Bleijenberg G, Swaen GM: Fatigue among working people: validity of a questionnaire measure.Occup Environ Med 2000,57(5):353–357.PubMedView Article
Drummond MF, Sculpher MJ, Torrance GW, O'Brien BJ, Stoddart GL: Methods for the economic evaluation of health care programmes. Third edition. Oxford: Oxford University Press; 2005.
Oostenbrink JB, Bouwmans CAM, Koopmanschap MA, Rutten FFH: Handleiding voor kostenonderzoek; methoden en standaard kostprijzen voor economische evaluaties in de gezondheidszorg. Amstelveen: Instituut voor Medical Technology Assessment, Erasmus MC in opdracht van College voor Zorgverzekeringen; 2004.
Briggs AH: Handling uncertainty in economic evaluation and presenting the results. In Economic evaluation in health care: merging theory with practice. Edited by: Drummond MF, McGuire A. Oxford: Oxford University Press; 2001:172–214.
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