Literature DB >> 27637569

Orthopaedic manifestations of congenital indifference to pain with anhidrosis (Hereditary Sensory and Autonomic Neuropathy type IV).

Babar Kayani1, Mathew David Sewell2, Johnson Platinum1, Andre Olivier1, Timothy W R Briggs1, Deborah M Eastwood1.   

Abstract

BACKGROUND: Congenital indifference to pain with anhidrosis (CIPA) is a rare hereditary neuropathy, which is associated with defective sensation to noxious stimuli and autonomic dysfunction. The objective of the study was to report on the orthopaedic manifestations of this condition and provide an evidence-based approach for management.
METHODS: Retrospective review of 14 consecutive patients with CIPA referred to a single tertiary centre. Mean age of diagnosis was 2.5 years (range 0.5 to 11 years).
RESULTS: Patients presented with a range of orthopaedic problems including fractures, infections, growth disturbance, joint subluxation and Charcot joints affecting the limbs and spine. Conservative treatment with closed reduction and cast immobilisation was satisfactory for stress fractures of the lower extremity and Charcot joints. Posterior instrumented correction of scoliosis was associated with a high-risk of infection requiring reoperation for debridement and removal of posterior instrumentation. Growth disturbance leading to leg-length discrepancies were managed with shoe raises and corrective osteotomies. Aspiration and cultures may be used to differentiate between acute fracture and infection.
CONCLUSIONS: Preventative treatment strategies with appropriately padded shoe-wear, gait and posture modification, parental education regarding environmental thermoregulation, and behavioural support are essential for improving prognosis and reducing long-term complications.
Copyright © 2016 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anhidrosis; Autonomic neuropathy; Charcot joint; Dislocation; Fracture; Growth; Neuropathy; Orthopaedic

Mesh:

Year:  2016        PMID: 27637569     DOI: 10.1016/j.ejpn.2016.08.009

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  5 in total

1.  Office-Based Anesthetic and Oral Surgical Management of a Child With Hereditary Sensory Autonomic Neuropathy Type IV: A Case Report.

Authors:  Shamit Prabhu; Kevin Fortier; Lisa Newsome; Uday N Reebye
Journal:  Anesth Prog       Date:  2018

Review 2.  Charcot spinal arthropathy in patients with congenital insensitivity to pain: a report of two cases and review of the literature.

Authors:  Michael D Staudt; Christopher S Bailey; Fawaz Siddiqi
Journal:  Neurosurg Rev       Date:  2017-01-26       Impact factor: 3.042

Review 3.  Genetic pain loss disorders.

Authors:  Annette Lischka; Petra Lassuthova; Arman Çakar; Christopher J Record; Jonas Van Lent; Jonathan Baets; Maike F Dohrn; Jan Senderek; Angelika Lampert; David L Bennett; John N Wood; Vincent Timmerman; Thorsten Hornemann; Michaela Auer-Grumbach; Yesim Parman; Christian A Hübner; Miriam Elbracht; Katja Eggermann; C Geoffrey Woods; James J Cox; Mary M Reilly; Ingo Kurth
Journal:  Nat Rev Dis Primers       Date:  2022-06-16       Impact factor: 65.038

4.  A 10-year follow-up of asymptomatic Charcot hip joints caused by CIPA syndrome (congenital insensitivity to pain with anhidrosis) with failure of any surgical reconstructive treatment.

Authors:  Ioannis Delniotis; Benedikt Leidinger
Journal:  J Surg Case Rep       Date:  2019-05-28

Review 5.  Key concepts in children's footwear research: a scoping review focusing on therapeutic footwear.

Authors:  Matthew Hill; Aoife Healy; Nachiappan Chockalingam
Journal:  J Foot Ankle Res       Date:  2019-04-27       Impact factor: 2.303

  5 in total

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