Literature DB >> 25551782

Preliminary Results of Multiple Epiphyseal Drilling and Autologous Bone Marrow Implantation for Osteonecrosis of the Femoral Head Secondary to Sickle Cell Disease in Children.

Eduardo N Novais1, Wudbhav N Sankar, Lawrence Wells, Patrick M Carry, Young-Jo Kim.   

Abstract

BACKGROUND: Sickle cell disease (SCD) is the most common cause of osteonecrosis of the femoral head (ONFH) during childhood. The natural history of ONFH in SCD is poor with progression to femoral head collapse and deformity that ultimately may lead to hip osteoarthritis. Multiple epiphyseal drilling with autologous bone marrow implantation may enhance the mechanism of osteogenic repair. The purpose of this study was to describe early clinical and radiographic outcomes in pediatric patients with ONFH secondary to SCD after multiple epiphyseal drilling and AMBI.
METHODS: Nine boys and 2 girls (14 hips) with a mean age of 12.7 years (range, 9.7-18 y) at the time of surgery were evaluated. All patients were followed for at least 1 year after surgery and the mean duration of follow-up was 25 months (range, 12-47 mo). Clinical outcome was assessed by the pain domain from the Children's Hospital Oakland Hip Evaluation Scale and by hip range of motion. The extent of femoral head involvement was assessed by measuring the arc of necrosis and the amount of collapse on anteroposterior and frog lateral radiographs. The University of Pennsylvania system was used to assess the osteonecrosis stage. Wilcoxon signed-rank tests were used to compare radiographic and clinical variables.
RESULTS: Compared with preoperative measures, multiple epiphyseal drilling with AMBI resulted in significant improvement in pain (P=0.0010), internal hip rotation (P=0.0005), external hip rotation (P=0.0010), and flexion (P=0.0015). The amount of lateral collapse (P=0.4609), anterior collapse (P=0.4258), and the arc of necrosis (P=0.2251) were not significant after surgery. The majority of the hips had either improvement in the Steinberg stage of disease (4/14 hips) or no further progression (7/14 hips) at the latest follow-up. There were no surgical complications.
CONCLUSIONS: Multiple epiphyseal drilling with autologous bone marrow cell implantation allows for short-term clinical improvement and limits radiographic progression of ONFH associated with SCD in children with minimal morbidity.

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Year:  2015        PMID: 25551782     DOI: 10.1097/BPO.0000000000000381

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  6 in total

1.  Regenerative therapies increase survivorship of avascular necrosis of the femoral head: a systematic review and meta-analysis.

Authors:  Luca Andriolo; Giulia Merli; Carlos Tobar; Sante Alessandro Altamura; Elizaveta Kon; Giuseppe Filardo
Journal:  Int Orthop       Date:  2018-02-06       Impact factor: 3.075

Review 2.  Operative Management of Avascular Necrosis of the Femoral Head in Skeletally Immature Patients: A Systematic Review.

Authors:  Filippo Migliorini; Gerardo La Padula; Francesco Oliva; Ernesto Torsiello; Frank Hildebrand; Nicola Maffulli
Journal:  Life (Basel)       Date:  2022-01-26

Review 3.  Nontraumatic Osteonecrosis of the Femoral Head: Where Do We Stand Today?: A 5-Year Update.

Authors:  Michael A Mont; Hytham S Salem; Nicolas S Piuzzi; Stuart B Goodman; Lynne C Jones
Journal:  J Bone Joint Surg Am       Date:  2020-06-17       Impact factor: 6.558

4.  IGF-1 polymorphisms modulate the susceptibility to osteonecrosis of the femoral head among Chinese Han population.

Authors:  Jun Wang; Hongyun Liu; Qiliang Zhang
Journal:  Medicine (Baltimore)       Date:  2019-06       Impact factor: 1.817

5.  Management of osteonecrosis of the femoral head in children with sickle cell disease: results of conservative and operative treatments at skeletal maturity.

Authors:  C Mallet; A Abitan; C Vidal; L Holvoet; K Mazda; A-L Simon; B Ilharreborde
Journal:  J Child Orthop       Date:  2018-02-01       Impact factor: 1.548

Review 6.  Why, Who, When, and How? Rationale for Considering Allogeneic Stem Cell Transplantation in Children with Sickle Cell Disease.

Authors:  Françoise Bernaudin
Journal:  J Clin Med       Date:  2019-09-22       Impact factor: 4.241

  6 in total

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