CHILDREN S ORTHOPAEDICS

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1 CHILDREN S ORTHOPAEDICS Cost-effectiveness of universal ultrasound screening compared with clinical examination alone in the diagnosis and treatment of neonatal hip dysplasia in Austria M. Thaler, R. Biedermann, J. Lair, M. Krismer, F. Landauer From the Medical University of Innsbruck, Innsbruck, Austria Between 1978 and 1997 all newborns in the Austrian province of Tyrol were reviewed regarding hip dysplasia and related surgery. This involved a mean of 8257 births per year (7766 to 8858). Two observation periods were determined: 1978 to 1982 (clinical examination alone) and 1993 to 1997 (clinical examination and universal ultrasound screening). A retrospective analysis compared the number and cost of interventions due to hip dysplasia in three patient age groups: A, 0 to < 1.5 years; B, 1.5 to < 15 years; and C, 15 to < 35 years. In group A, there was a decrease in hip reductions from a mean of 25.2 (SD 2.8) to 7.0 (SD 1.4) cases per year. In group B, operative procedures decreased from a mean of 17.8 (SD 3.5) to 2.6 (SD 1.3) per year. There was a 75.9% decrease in the total number of interventions for groups A and B. An increase of in the overall cost per year for the second period (1993 to 1997) was seen, mainly due to the screening programme. However, there was a marked reduction in costs of all surgical and non-surgical treatments for dysplastic hips from (1978 to 1982) to (1993 to 1997). We believe the small proportional increase in costs of the universal ultrasound screening programme is justifiable as it was associated with a reduction in the number of non-surgical and surgical interventions. We therefore recommend universal hip ultrasound screening for neonates. M. Thaler, MD, Resident R. Biedermann, MD, Associate Professor J. Lair, MD, Resident M. Krismer, MD, Professor, Head of Department Department of Orthopaedic Surgery Medical University of Innsbruck, Anichstrasse 65, 6020 Innsbruck, Austria. F. Landauer, MD, Consultant Department of Orthopaedic Surgery Private Medical University Salzburg, Müllner Hauptstrasse 48, A-5020 Salzburg, Austria. Correspondence should be sent to Dr F. Landauer; f.landauer@salk.at 2011 British Editorial Society of Bone and Joint Surgery doi: / x.93b $2.00 J Bone Joint Surg [Br] 2011;93-B: Received 22 September 2010; Accepted after revision 14 April 2011 Developmental dysplasia of the hip (DDH), with its potential for early osteoarthritis, is the most common congenital defect in newborns, with an incidence of approximately 1.4 per 1000 births in Caucasions. 1-3 In recent decades the traditional clinical screening for DDH has increasingly included ultrasonography. 4,5 Although several studies have described sonography as the most reliable diagnostic method, 6-9 there is no consensus regarding its universal use Some authors recommend selective ultrasound for cases with risk factors or clinical signs of dysplasia or dislocation. 14 Some countries, such as Austria, have established universal screening programmes for the newborn 15 while others prefer selective screening for hip dysplasia. 16 Neither method carries iatrogenic risk and irrespective of which is used, early diagnosis through screening and early treatment have lowered the overall number of subsequent operations. 17,18 However, there is ongoing debate about the preferred screening method. Whereas reports from countries with an established universal ultrasound screening programme encourage its use, 19 others do not confirm its superiority. 14 There is little published data concerning cost analysis when comparing clinical examination alone with clinical examination and ultrasound screening In the Austrian province of Tyrol, clinical examination alone was performed between 1978 and Between 1983 and 1988, a nationwide ultrasound screening programme according to Graf 6 was developed throughout Austria and since 1988 ultrasound screening has been performed for all newborn babies. The aim of this study was to investigate the influence of the screening method on the costs incurred by the healthcare system due to DDH. Patients and Methods In our hospital, between 1978 and 1982, a routine clinical examination according to Ortolani 23 and Barlow 24 was performed in all babies within the first week of life by a trained paediatric orthopaedic surgeon. In a case of suspected DDH, radiological examination was 1126 THE JOURNAL OF BONE AND JOINT SURGERY

2 COST-EFFECTIVENESS OF UNIVERSAL ULTRASOUND SCREENING COMPARED WITH CLINICAL EXAMINATION 1127 added. After discharge, all infants with abnormal clinical signs or risk factors of positive family history or breech birth were re-examined at the age of six to eight weeks and an x-ray taken if clinically suspicious and, if necessary, infants were treated in our hospital. Those infants with unremarkable findings at this time were followed up by an orthopaedic surgeon for a further period of between six and eight weeks. A nationwide ultrasound screening programme was developed between 1983 and Since then, ultrasound screening using the Graf method 6 combined with clinical examination is part of a National Health Programme plan (NHP) for newborns and babies. All are screened within a week of birth by a trained paediatric orthopaedic surgeon. After discharge, all infants with unremarkable hips are routinely followed up by an orthopaedic surgeon for six to eight weeks as part of the NHP plan, while those with abnormal clinical or sonographic findings or risk factors (positive family history, breech birth) are also reviewed clinically at the age of six to eight weeks, and undergo further sonographic evaluation of the hips. For the study, two observation periods were determined. Period I (clinical examination alone) was between 1 January 1978 and 31 December Period II (universal ultrasound and clinical examination) was between 1 January 1993 and 31 December In period I, infants ( males, females) were included, compared with ( males, females) in period II. The period between 1983 and 1993 was excluded to minimise bias due to the learning experience associated with the introduction of the ultrasound screening programme. A retrospective analysis of the two periods was performed regarding surgical treatment and costs. During the overall observation period the indications for surgery did not change. However, new operations such as the periacetabular osteotomy were introduced. 25 For all patients, the treatment protocol recommended by Graf 15 was used. Patients with hip dysplasia secondary to conditions such as neuromuscular disorders or Perthes' disease were excluded. According to age-dependent treatment principles, three patient samples were determined encompassing the following age ranges: group A, 0 to < 1.5 years; group B, 1.5 to < 15 years; and group C, 15 to < 35 years of age. The annual birth rate in the province was recorded, as published by Statistics Austria. 26 From the hospital database we obtained the number of clinical follow-up examinations per child, the number of open and closed reductions, the number and type of operation per child and group of children and number of splinting devices used. The costs for operative and conservative treatment, ultrasound examination and clinical investigations were obtained from the national health insurance fund. The costs of the splints were provided by the manufacturer. The Pavlik harness 27 (Danner, Innsbruck, Austria) (average two per child) was used between between 1978 and 1982 and the Tuebinger bandage 28 (Ottobock, Duderstadt, Germany) (one per child) between 1993 and The costs of hospital admissions for closed reductions and open operations were calculated on the basis of the procedures undertaken, duration of hospital stay and specialty-specific costs per in-patient day. It was calculated that a single closed reduction cost 3000, which included the operating theatre occupancy, anaesthesia, theatre staff, and number and type of staff involved during casting, and clinical and radiological follow-up. In a similar way it was calculated that the mean cost of a single operation, such as varus derotation or pelvic osteotomy, was Arthroplasty of the hip was not included. The costs of hospital in-patient admissions were based on national reference costs for surgical procedures, clinical and radiological follow-ups and hospital-specific costs per in-patient day. The mean costs for outpatient consultations were assumed to be 500 per child for both observation periods, including staff in attendance, clinical follow-up examinations and radiological follow-ups. The overall cost of ultrasound examination in hospital was This was derived from the time and personnel per investigation and cost of equipment. The overall cost of ultrasonographic examinations by orthopaedic surgeons at outpatient visits was This was calculated according to reimbursements from the national health insurance. The data were processed using the Statistical Package for Social Sciences v.13 (SPSS Inc., Chicago, Illinois). Results From 1978 to 1997 there were live births representing a mean of 8257 per year (7766 to 8858). According to the Austrian Ministry of Health, 96% of all newborns were included during both study periods. 7 With the introduction of ultrasound hip screening, the rate of splintage dropped from a mean of 170 cases per year (147 to 190) in period I to a mean of 90 per year (82 to 105) in period II. When comparing the age at which treatment was instigated between the two periods, there was a decrease in hip reductions from a mean of 25.2 (SD 2.8) cases per year in period I to a mean of 7.0 (SD 1.4) in period II in group A. In group B, there was a decrease in surgical procedures for dysplastic hips from a mean of 17.8 (SD 3.5) to a mean of 2.6 (SD 1.3) per year for periods I and II, respectively. A slight reduction in the number of operations for dysplastic hips was seen in the oldest patients of group C (Fig. 1). In period I, a total of 105 pelvic osteotomies and varus derotation osteotomies were performed, compared with 76 operations for the same indications in period II. Since the introduction of universal hip ultrasound screening, the decrease in the number of interventions for groups A and B (combined age range 0 to < 15 years) was 75.9% (Table I). The comparison of costs between the periods showed an overall increase in the costs of screening and treatment for DDH of per year between 1993 and 1998, which was mainly due to VOL. 93-B, No. 8, AUGUST 2011

3 1128 M. THALER, R. BIEDERMANN, J. LAIR, M. KRISMER, F. LANDAUER Cases per year Closed reductions Open reductions Group B (VDRO/pelvic osteotomies) Group C (VDRO/pelvic osteotomies) Fig. 1 Interventions for hip dysplasia during the two periods for three patient samples group A: 0 to < 1.5 years (closed and open reductions), group B: 1.5 to < 15 years (VDRO: varus derotation osteotomy, pelvic osteotomies), group C: 15 to < 35 years (VDRO, pelvic osteotomies). Table I. Comparison of total number of surgical interventions between the two observation periods (VDRO, varus derotation osteotomy) Age group 1978 to to 1997 A (0 to < 1.5 years) Closed reductions Open reductions 14 7 B ( 1.5 to < 15 years) Acetabular osteotomies/vdros C ( 15 to 35 years) Acetabular osteotomies/vdros Table II. Comparison of mean costs in Euros between the study periods 1978 to to 1997 Service Cost (Euros per year) Service Cost (Euros per year) Pavlik harness Tuebinger bandage Clinical follow-up Clinical follow-up examinations examinations Closed reduction Closed reduction Surgery Surgery Ultrasound screening Total costs of interventions Total costs the ultrasound programme (Table II). However, there was a considerable cost reduction regarding operative and non-operative treatment for dysplastic hips from (1978 to 1982) to (1993 to 1997). Discussion The economic evaluation of treatment regimes is of increasing importance in times of escalating healthcare budgets. It is proposed that early diagnosis of DDH allows THE JOURNAL OF BONE AND JOINT SURGERY

4 COST-EFFECTIVENESS OF UNIVERSAL ULTRASOUND SCREENING COMPARED WITH CLINICAL EXAMINATION 1129 comparably cheap treatment with a simple brace 18,29 and that delayed diagnosis carries a greater risk for surgical treatment at a later stage. 17,30,31 It is reported that 15% of all infants have more than one risk factor for DDH 14 and risk factors are seen in 40% of newborns with a clinically detectable abnormality of the hip. 11,32 Previous studies have shown a low incidence of late-detected hip dysplasia after ultrasound screening of newborns. In a group of infants Marks, Clegg and al-chalabi 33 found no case and Rosendahl, Markestad and Lie 34 reported one case of late detection in a selective ultrasound screening group, two in a group screened only clinically, but no cases in a universal ultrasound screening group. When evaluating the cost-effectiveness of hip ultrasound screening, Gray et al 21 showed significantly lower costs of splinting and lower costs to the family associated with surgery compared with the clinical examination group. The advantages of ultrasound screening are direct observation and dynamic assessment in the evaluation of the newborn hip. However, knowledge and practice are needed to obtain reliable results and false-positive results lead to overtreatment. 10,34-36 In our study, the splintage rate controversially dropped with the introduction of hip ultrasound whereas clinical examination alone was associated with a higher treatment rate. The mean decrease in hip reductions was due to successful primary splintage in cases of sonographically detected abnormal hips. In a prospective randomised trial, after a follow-up of six to 11 years, Holen et al 14 found no statistically significant difference for latedetected hip dysplasia between children receiving ultrasound screening (n = 1) and those having clinical examination alone (n = 5). Consequently, they considered universal ultrasound screening unnecessary, but recommended selective ultrasound screening for neonates with abnormal or suspicious clinical findings and those with risk factors for hip dysplasia. These authors presented data only for latedetected hip dysplasia and no intermediate findings, such as the number of additional clinical follow-ups or the number of splinting devices, were described. Furthermore, they used the ultrasound screening method as described by Terjesen et al 5 and Holen et al, 37 whereas recent studies have shown better intra-observer reliability for the Graf method, 38 which is strictly standardised, 39 but requires teaching and experience to avoid misdiagnosis. 31 The results in other studies might have been influenced because patients were included during the learning period. 14 The best timing for hip ultrasound screening is debatable. Graf 39 recommends early screening to allow treatment during the peak growth of the acetabulum, which has a high potential of remodelling as form follows function. Conversely, early screening leads to more false positive results. 14 Hence, Grill and Müller 19 recommend the sixth to eighth week as the optimal time, which was implemented in the Austrian screening programme. According to the Austrian Ministry of Health, 96% of newborn babies are screened. This high rate is due to a pregnancy and early-childhood medical record book. Several investigations, including hip sonography, are compulsory and predetermined in the pregnancy and early-childhood medical record book and linked to a federal premium. The province of Tyrol has a mixed urban-rural population with one major city with over inhabitants in the centre. There are ultrasound facilities for hip screening of the newborn in each of the eight district hospitals in the county. Ultrasound screening at the age of six to eight weeks is performed by every orthopaedic surgeon in private practice in the county. A recent report 20 demonstrated that newborns screened with ultrasonography incurred significantly higher costs over the first two years compared with those who underwent clinical screening alone. The total hospital costs were lower for the infants screened with ultrasound, but the difference was not especially marked. The study also showed that ultrasound screening reduced the splintage rates, but was not associated with abnormal hip development or higher rates of surgical treatment by two years of age. 20 Differences between healthcare systems, with regard to their financing, management, clinical practice and costs, limit direct comparison among different countries without appropriate adjustments. However, our results should be of interest in countries without a universal hip screening programme. This study shows higher initial costs caused by the ultrasound screening, but also a significant reduction in the total number and overall costs of dysplastic hips undergoing operative and non-operative treatment. Similar findings were reported by Clegg et al, 22 who compared the surgical costs of three screening methods for DDH: universal clinical examination alone, universal clinical examination with selective ultrasound examination for newborn babies with risk factors, and universal ultrasound screening. The mean costs per 1000 live births were 5110 for clinical investigation alone, 3811 for selective ultrasound screening, and 468 for universal ultrasound screening. With the addition of the costs of surgical treatment, the overall costs were comparable among the different methods. In our view ultrasonographic evaluation reduces uncertainty and may reduce further costs to health services and affected families. Alongside this, important non-financial aspects, such as psychological factors, should be considered. Listen live Listen to the abstract of this article at No benefits have been received or will be received from a commercial party related directly or indirectly to the subject of this article. References 1. Felson DT, Zhang Y. An update on the epidemiology of knee and hip osteoarthritis with a view to prevention. Arthritis Rheum 1998;41: Harris WH. Etiology of osteoarthritis of the hip. Clin Orthop 1986;213: Mahan ST, Katz JN, Kim YJ. To screen or not to screen?: a decision analysis of the utility of screening for developmental dysplasia of the hip. J Bone Joint Surg [Am] 2009;91-A: Graf R, Tschauner C. Sonography of the infant hip: sources of error, progress and current clinical relevance. Radiologe 1994;34:30-8 (in German). VOL. 93-B, No. 8, AUGUST 2011

5 1130 M. THALER, R. BIEDERMANN, J. LAIR, M. KRISMER, F. LANDAUER 5. Terjesen T, Bredland T, Berg V. Ultrasound for hip assessment in the newborn. J Bone Joint Surg [Br] 1989;71-B: Graf R. Classification of hip joint dysplasia by means of sonography. Arch Orthop Trauma Surg 1984;102: Krismer M, Klestil T, Morscher M, Eggl H. The effect of ultrasonographic screening on the incidence of developmental dislocation of the hip. Int Orthop 1996;12: Tönnis D, Storch K, Ulbrich H. Results of newborn screening for CDH with and without sonography and correlation of risk factors. J Pediatr Orthop 1990;10: Wientroub S, Grill F. Ultrasonography in developmental dysplasia of the hip. J Bone Joint Surg [Am] 2000;82-A: Castelein RM, Sauter AJ, de Vlieger M, van Linge B. Natural history of ultrasound hip abnormalities in clinically normal newborns. J Pediatr Orthop 1992;12: Clarke NM, Clegg J, Al-Chalabi AN. Ultrasound screening of hips at risk for CDH: failure to reduce the incidence of late cases. J Bone Joint Surg [Br] 1989;71-B: Riboni G, Bellini A, Serantoni S, Rognoni E, Bisanti L. Ultrasound screening for developmental dysplasia of the hip. Pediatr Radiol 2003;33: Schuler P, Feltes E, Kienapfel H, Griss P. Ultrasound examination for the early determination of dysplasia and congenital dislocation of neonatal hips. Clin Orthop 1990;258: Holen KJ, Tegnander A, Bredland T, et al. Universal or selective screening of the neonatal hip using ultrasound?: a prospective, randomised trial of 15,529 newborn infants. J Bone Joint Surg [Br] 2002;84-B: Graf R. Fundamentals of sonographic diagnosis of infant hip dysplasia. J Pediatr Orthop 1984;4: Boeree NR, Clarke NM. Ultrasound imaging and secondary screening for congenital dislocation and dysplasia of the hip. J Bone Joint Surg [Br] 1994;76-B: MacKenzie IG, Seddon HJ, Trevor D. Congenital dislocation of the hip. J Bone Joint Surg [Br] 1960;42-B: Tredwell SJ, Bell HM. Efficacy of neonatal hip examination. J Pediatr Orthop 1981;1: Grill F, Müller D. Results of hip ultrasonographic screening in Austria. Orthopade 1997;26:25-32 (in German). 20. Elbourne D, Dezateux C, Arthur R, et al; UK Collaborative Hip Trial Group. Ultrasonography in the diagnosis and management of developmental hip dysplasia (UK Hip Trial): clinical and economic results of a multicentre randomised controlled trial. Lancet 2002;360: Gray A, Elbourne D, Dezateux C, et al. Economic evaluation of ultrasonography in the diagnosis and management of developmental hip dysplasia in the United Kingdom and Ireland. J Bone Joint Surg [Am] 2005;87-A: Clegg J, Bache CE, Raut VV. Financial justification for routine ultrasound screening of the neonatal hip. J Bone Joint Surg [Br] 1999;81-B: Ortolani M. Un segno poco noto e sua importanza per la diagnosi precoce di prelussazione conenita dell anca. Pediatrica 1937;45: (in Italian). 24. Barlow TG. Early diagnosis and treatment of congenital dislocation of the hip. J Bone Joint Surg [Br] 1962;44-B: Ganz R, Klaue K, Vinh TS, Mast JW. A new periacetabular osteotomy for the treatment of hip dysplasias: technique and preliminary results, Clin Orthop 2004;418: No authors listed. Statistik Austria: demographische Indikatoren für Tirol. (date last accessed 15 June 2011). 27. Atalar H, Sayli U, Yavuz OY, Uras I, Dogruel H. Indicators of successful use of the Pavlik harness in infants with developmental dysplasia of the hip. Int Orthop 2007;31: Hefti F. Kongenitale Hütdysplasie und -luxation. In: Kinderorthopädie in der Praxis. Vol. 2. Heidelberg: Springer, 2009: Harding MG, Harcke HT, Bowen JR, Guille JT, Glutting J. Management of dislocated hips with Pavlik harness treatment and ultrasound monitoring. J Pediatr Orthop 1997;17: Trevor D. Congenital dislocation of the hip. Ann R Coll Surg Engl 1972;50: von Kries R, Ihme N, Oberle D, et al. Effect of ultrasound screening on the rate of first operative procedures for developmental hip dysplasia in Germany. Lancet 2003;362: Walter RS, Donaldson JS, Davis CL, et al. Ultrasound screening of high-risk infants: a method to increase early detection of congenital dysplasia of the hip. Am J Dis Child 1992;146: Marks DS, Clegg J, al-chalabi AN. Routine ultrasound screening for neonatal hip instability: can it abolish late-presenting congenital dislocation of the hip? J Bone Joint Surg [Br] 1994;76-B: Rosendahl K, Markestad T, Lie RT. Ultrasound screening for developmental dysplasia of the hip in the neonate: the effect on treatment rate and prevalence of late cases. Pediatrics 1994;94: Terjesen T, Holen KJ, Tegnander A. Hip abnormalities detected by ultrasound in clinically normal newborn infants. J Bone Joint Surg [Br] 1996;78-B: Kocher MS. Ultrasonographic screening for developmental dysplasia of the hip: an epidemiologic analysis (Part I). Am J Orthop (Belle Mead NJ) 2000;29: Holen KJ, Terjesen T, Tegnander A, et al. Ultrasound screening for hip dysplasia in newborns. J Pediatr Orthop 1994;81: Falliner A, Schwinzer D, Hahne HJ, Hedderich J, Hassenpflug J. Comparing ultrasound measurements of neonatal hips using the methods of Graf and Terjesen. J Bone Joint Surg [Br] 2006;88-B: Graf R. Hip ultrasonography: basic principles and current aspects. Orthopade 1994;26:14-24 (in German). THE JOURNAL OF BONE AND JOINT SURGERY

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