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Fırat Üniversitesi Sağlık Bilimleri Tıp Dergisi
2019, Cilt 33, Sayı 1, Sayfa(lar) 047-050
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Kapalı Redüksiyon ve Pelvipedal Alçı Uygulanan DDH Hastalarda MPV Avasküler Nekroz için Belirteç midir?
İsmail Hakkı KORUCU, Burkay Kutluhan KAÇIRA
Necmettin Erbakan University, Faculty of Meram Medicine, Department of Orthopedics, Konya, TURKEY
Anahtar Kelimeler: Kapalı redüksiyon, avasküler nekroz, ortalama trombosit hacmi
Özet
Amaç: Kapalı redüksiyon (KR) ve pelvipedal alçılama (PPA) gelişimsel kalça displazisinde iyi bir seçenektir. Komplikasyon oranları %79’lara ulaşabilmektedir ve avaskuler nekroz (AVN) özellikle problemlidir. AVN’nin tam nedeni bilinmemektedir ve çok faktörlüdür. Trombosit aktivitesi, trombosit hacmi yani ortalama trombosit hacmi (OTH) olarak ölçülür. Çalışmanın amacı trombosit hacim değişimlerinin femur başına etkilerinin olup olmadığını araştırmaktır.

Gereç ve Yöntem: N.E. Üniversitesi Meram Tıp Fakültesi hastanesinde 2013 ila 2017 yılları arası KR PPA yapılan hastalar retrospektif incelendi. Ameliyat öncesi sonrası ve 1. ay tam kan sayımları ve MPV incelendi. Hastalar yaşlara göre 4 gruba ayrıldı; Grup 1 doğum–6. ay, Grup 2 7–12. ay, Grup 3 13–18. ay ve Grup 4 18 ay sonrası.

Bulgular: Hastalar ortalama 40.5 ay (16–66) takip edildi. 39 hastanın 43 kalçası KR ve PPA ile tedavi edildi. AVN 8 hastada görüldü (%18.6) AVN li hastalarda erken ameliyat sonrası dönemde MPV artmış bulundu.

Sonuç: MPV, KR ve PPA uygulanan GKD li hastalarda önceden tahmin etmemize yararlı olabilir. Erken ameliyat sonrası dönem MPV yüksekliği olan hastaların AVN gelişimi açısından daha yakın takibi önerilir.

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    Developmental dysplasia of the hip (DDH) has an estimated incidence of 1.5–20 per 1000 births 1. The aim of treatment for DDH is to obtain a stable and concentric reduction in the hip. Closed reduction (CR) and spica cast immobilization under general anesthesia areprovide a good reduction 2,3. Complication rates have been reported as high as 79%, and avascular necrosis (AVN) has proven to be particularly problematic. This major complication has a reported incidence of up to 47% and can result in limblength discrepancy, joint incongruity, persistent subluxation, coxa valga, and other sequelae 4. Altough many factors play role on developing AVN, the exact etiology of AVN is unknown but likely multifactorial. Among of them thrombotic activity is important 5.

    Thrombocyte volume has been defined as a marker of thrombocyte activation and function and it is measured as mean platelet volume (MPV). MPV shows the mean volume of circulating thrombocytes and it is one of the routine parameters in complete blood count. Increased thrombocyte volüme is associated with thrombocyte activation.

    There is a relation between AVN and high trombositic activity 6. We hypothesized that AVN after treated with closed reduction and spica casting DDH is related to MPV.

    The aim of this study was to investigate whether thrombocyte volume changes affect the femoral head’s development after closed reduction of DDH.

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    We reviewed the medical records of all patients who underwent closed reduction of the hip for DDH at Necmettin Erbakan University Meram School of Medicine Hospital from 2013 to 2017. Inclusion criteria were diagnosed with DDH and treated with closed reduction and spica cast under general anesthesia, diagnosis of AVN according to the criteria given by Salteret et al. 7’s. Exclusion criteria was diagnosed with neuromuscular, malformation, deformity, syndromic disorders, and other similar diagnoses and underwent a surgical procedure requiring opening of the capsule of the hip joint within 1 year after the initial closed reduction.

    All patients with DDH was operated by the same surgeon. Under general anesthesia hips were reduced closed fashion and spica cast immobilisation was performed. The range of motion within safe zone limits were checked for all hips. The spica cast was applied with the hip held in 100° of flexion and 70° of abduction, but never in forcedabduction. Spica cast duration was 3 months. No traction was applied to any patient preoperatively.

    Demographic data were obtained, including sex, side of DDH, side of AVN of the femoral head, age at reduction, interval between the reduction and presence of AVN, the presence of the femoral head ossific nucleus. Hips were classified on the basis of Tönnis’s classification 8. The pelvis X-rays at final follow up were evaluated andgraded on the basis of Kalamchi and MacEwen (9)’s classification. Pre- and early postoperative and at first month complete blood counts (CBC) were collected and recorded MPV values. At the final follow up duration MPV value also was recorded.

    We divided all patients in four groups in terms of age as Group 1 birth to 6th month, Group 2 7th to 12 month, Group 3 13th to 18 month and Group 4 older than 18 month. The data collected were processed for statistical analysis using the SPSS statistical software package, version 16.0.

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    Patients are followed up 40.5 months (16-66). Demographic and baseline data are presented in Table 1 39 patients were included and 43 hips were treated with closed reduction and spica cast. AVN was occured in 8 patients (18.6%) and shown in Table 2. No patients had bilateral AVN.


    Büyütmek İçin Tıklayın
    Table 1: Demographic and baseline data


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    Table 2: Results of AVN based on the classification of Kalamchi and MacEwen 9

    MPV values of the patients with AVN or no AVN are presented in Table 3. In patients with AVN, MPV increased at early postoperative period and first month. This increase was statistically significant (P<0.05). Between the patients with AVN and noAVN, MPV levels were observed as also statistically significant (P<0.05).

    There was not relation between MPV and other parameters (age, sex, side, Kalamchi and MacEwen 9 types, presence of the femoral head ossific nucleus, Tönnis classification).


    Büyütmek İçin Tıklayın
    Table 3: MPV values

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    Our study showed that MPV can be a predictive value for AVN for DDH patients who were treated with closed reduction and hip spica casting. Especially, at the early postoperative period, MPV increasing was significant.

    Several studies have been tried to determinepredictive values in an effort to predict the severity of AVN or growth disturbance 5. These studies have cited various possible risk factors of AVN, including age, gender, laterality, absence of proximal femoral ossific nucleus, use ofpre-reduction traction, preliminary/history of hip abduction bracing, adductor tenotomy, and hip abduction angle incast 7,11-16. AVN is still the main concern following the treatment of DDH by closed reduction and cast immobilization. The reported rate of AVN ranges from 0 to 67%. Brougham et al. 15 reported on 184 patients who underwent closed reduction of 210 hip dislocations and noted AVN in 99 (of 210 affected hips, 47%). In the studies of Herold et al. (450 hips) 17, Gregosiewicz et al. (1211 hips) 18 and Kruczynskiet al. (823 hips) 19, the reported incidences of AVN were12, 21, and 14%, respectively, and the mean AVN rate ofthese studies was 17%. In our study AVN rate was found %18.6. Risk of AVN was unaffected by age, gender, laterality, previous use of hip abduction orthosis, or adductor tenotomy 15,19,21.

    There is no study in the literature including relationship between femoral head AVN and MPV. Increase of platelet count and activation may be important on hypercoagulopathy. 16 Any inflammatory stress generation during closed reduction and hip spica casting can trigger coagulobility. The increase in MPV was related to an increase in pro-inflammatory cytokine levels. TNF-α and IL-6 are the cytokines that cause osteonecrosis, and they are linked with enhanced oxidative stress, which contributes to platelet activation 20. This pathogenesis may explain the increase of MPV in the early postoperative period. MPV levels increased in all AVN patients. According to us, this finding is very important to explain the relation of MPV with AVN.

    The most important limitations of our study are its retrospective natüre and small sample size.

    In conclusion, MPV can be considered as a predictive parameter for avascular necrosis in patients with DDH who treated with closed reduction and spica cast. Checking the MPV levels in early postoperative period close follow-up can be an indicator for developing AVN.

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    1) Patel H. Canadian Task Force on Preventive Health Care Preventive health care, 2001 update: Screening and management of developmental dysplasia of the hip in newborns. CMAJ 2001; 164:1669-1677.

    2) Cooper AP, Doddabasappa SN, Mulpuri K. Evidence-based management of developmental dysplasia of the hip. Orthop Clin N Am 2014; 45: 341-354.

    3) Kotlarsky P, Haber R, Bialik V, Eidelman M Developmental dysplasia of the hip: What has changed in the last 20 years? World J Orthop 2015; 6: 886-901.

    4) Murray T, Cooperman DR, Thompson GH, Ballock RT. Closed reduction fortreatment of developmental dysplasia of the hip in children. Am J Orthop (Belle Mead NJ) 2007; 36: 82-84.

    5) Sibiński M, Synder M, Domzalski M, Grzegorzewski A. Risk factors foravascular necrosis after closed hip reduction in developmental dysplasiaof the hip. Ortop Traumatol Rehabil 2004; 6: 60-66.

    6) Martin JF, Shaw T, Heggie J, Penington DG. Measurement of the density of human platelets and its relationship to volume. Br J Haematol 1983; 54: 337-352.

    7) Salter RB, Kostuik J, Dallas S. Avascular necrosis of the femoral head asa complication of treatment for congenital dislocation of the hip in young children: A clinical and experimental investigation. Can J Surg 1969; 12: 44-61.

    8) Tonnis D. Congenital Dysplasia and Dislocation of the Hip in Children and Adults. Berlin: Springer-Verlag, 1987.

    9) Kalamchi A, MacEwen GD. Avascular necrosis following treatment ofcongenital dislocation of the hip. J Bone Joint Surg Am 1980; 62: 876-888.

    10) Casaletto JA, Perry DC, Foster A, Bass A, Bruce CE. The height-to-widthindex for the assessment of femoral head deformity following osteonecrosisin the treatment of developmental dysplasia. J Bone Joint Surg Am 2009; 91: 2915-2921.

    11) Gage JR, Winter RB. Avascular necrosis of the capital femoral epiphysis as a complication of closed reduction of congenital dislocation of the hip. A critical review of twenty years’ experience at Gillette Children’s Hospital. J Bone Joint Surg Am 1972; 54: 373-388

    12) Fogarty EE, Accardo NJ Jr. Incidence of avascular necrosisof the femoral head in congenital hip dislocation related to thedegree of abduction during preliminary traction. J Pediatr Orthop 1981; 1: 307-311.

    13) Clarke NM, Jowett AJ, Parker L. The surgical treatmentof established congenital dislocation of the hip: Results of surgeryafter planned delayed intervention following the appearanceof the capital femoral ossific nucleus. J Pediatr Orthop 2005; 25: 434-439.

    14) Segal LS, Boal DK, Borthwick L, et al. Avascular necrosis after treatment ofDDH: The protective influence of the ossific nucleus. J Pediatr Orthop 1999; 19: 177-184.

    15) Brougham DI, Broughton NS, Cole WG, Menelaus MB Avascular necrosis following closed reduction of congenital dislocation of the hip. Review of influencing factors and long-term follow-up. J Bone Joint Surg Br 1990; 72: 557-562.

    16) Bauvois B, Mothu N, Nguyen J, et al. Specific changes in plasma concentrations of matrix metalloproteinase-2 and -9, TIMP-1 and TGF-beta 1 in patients with distinct types of primary glomerulonephritis. Nephrol Dial Transplant 2007; 22: 1115-1122.

    17) Herold HZ. Avascular necrosis of the femoral head in congenitaldislocation of the hip. Isr J Med Sci 1980; 16: 295-300.

    18) Gregosiewicz A, Wosko I. Risk factors of avascular necrosisin the treatment of congenital dislocation of the hip. J Pediatr Orthop 1988; 8: 17-19.

    19) Kruczynski J. Avascular necrosis of the proximal femurin developmental dislocation of the hip. Incidence, risk factors, sequelae and MR imaging for diagnosis and prognosis. ActaOrthop Scand Suppl 1996; 268: 1-48

    20) Broudy VC, Lin NL, Fox N, et al. Thrombopoietin stimulates colony-forming unit-megakaryocyte proliferation and megakaryocyte maturation independently of cytokines that signal through the gp130 receptor subunit. Blood 1996; 88: 2026-2032.

    21) Köse N, Ömeroğlu H, Özyurt B, et al. Üç-dört haftalık bebeklerde yürütülen ultrasonografik kalça taraması programında üç yıllık deneyimimiz. Acta Orthop Traumatol Turc 2006; 40: 285-290.

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