PEARLS AND RESOURCES Growth and DevelopmentZCongenital Conditions
Pearls
■ An embryologic alteration of the musculoskeletal system often is a superficial marker for embryologic alterations in other organ systems.
■ Deferring radiography until a minimum of 6 months in age, allowing bones to ossify, is generally a good idea.
■ Malformations of the radius are more common and associated with more syndromes than malformations of the ulna.
■ To be a clubfoot, there must be hindfoot varus and adduction.
■ Cavus feet always need an explanation and can be a superficial sign of an underlying neurologic diagnosis.
Resources
Paley D, Bhavee A, Herzenberg JE, et al. Multiplier method for predicting limb length discrepancy. J Bone Joint Surg Am. 2000;82:1432-1446.
Abel MF. Orthopedic Knowledge Update. Rosemont, IL: American Academy of Orthopedic Surgeons;2006.
Ponseti IV. Congenital Clubfoot: Fundamentals of Treatment. Oxford: Oxford University Press;1996.
Coleman SS, Chestnut WJ. A simple test for hindfoot flexibility in the cavovarus foot. Clin Orthop. 1977;123:60-62.
Robinson RO. Arthrogryposis multiplex congenita: feeding, language and other health problems. Neuropediatrics. 1990;21:177.
Brachial Plexus Palsy
Pearls
■ The most common risk factors for a baby having a birth brachial plexus palsy (BBPP) are shoulder dystocia, large birth weights, and multiparous mothers.
■ It is critical for the caregivers to have the baby/tod- dler see/use the arm with BBPP as much as possible to minimize learned disuse.
■ A key difference between acquired BPP and BBPP is pain in the former and no pain in the latter (at least after the first two weeks).
■ Neuropraxia has no permanent anatomical changes and will resolve; axonotmesis (partial) and neurotmesis (complete) anatomical severance each has long-lasting sequelae.
■ Sensory nerve conduction studies in someone from an insensate area with intact SNAP indicate a preganglionic lesion.
Resources
Asa J, Wilbourn MD. Plexopathies. Neurol Clin. 2007;25: 139-171.
Gilbert A, Pivato G, Kheiralla T. Long-term results of primary
repair of brachial plexus lesions in children. Microsurgery. 2006:26:334-342.
Lee MY, Nelson M, Lee CE. Evaluation and management of brachial plexus injury. In: Lazar RB, ed. Principles of Neurologic Rehabilitation. New York” McGraw-Hill;1998: 230.
Seddon HJ. Three types of nerve injury. Brain. 1943; 66:34.
Waters PM. Comparison of natural history, the outcome of microsurgical repair, and the outcome of operative reconstruction in brachial plexus birth palsy. J Bone J Surg Am. 1999;81:649-659.
Children With Rheumatic Disease
Pearls
■ Juvenile idiopathic arthritis (JIA) occurs in children before the age of 16 years, persists at least six weeks, and has had other known conditions excluded.
■ Treatment of children with JIA is a team approach that focuses on eliminating inflammation, promoting developmentally appropriate function and activity, and minimizing complications.
■ JIA or its treatment can cause local or systemic abnormalities, including micrognathia, leg-length inequalities, muscle atrophy, short stature, osteoporosis, and increased risk of infection.
■ Enthesitis, uveitis, rash, fever, or lymphadenopathy may be the earliest signs/symptoms in children with JIA and/or juvenile ankylosing spondylitis.
■ Pediatric physiatrists can play a key role in the comprehensive management of the child with rheumatic conditions to maximize age-appropriate function, prevent deformity, and manage pain.
Resources
Cassidy JT, Petty RE, Laxer RM, et al. Textbook of PediatricRheumatology. 5thed.Philadelphia:Elsevier; 2005.
Davis PJC, McDonagh JE.Principles of management of musculoskeletal conditions in children and young people. Best Pract Res Clin Rheumatol. 2006; 20(2):263-278.
Szer IS, Kimura Y, Malleson PN, et al. Arthritis in Children and Adolescents.
New York: Oxford University Press;2006.Wallace CA. Current management of juvenile idiopathic arthritis. Best Pract Res Clin Rheumatol. 2006; 20(2):279-300.
Burn Injuries
Pearls
■ Children under 5 are more likely to sustain scald or contact burns, while older children and adolescents are more likely to sustain burns from flames.
? Refer to a burn center when a child has chemical, electrical, or third-degree burns; partial-thickness burns to 10% total BSA; burns to sensitive body parts; inhalation injury; or complicating medical factors.
■ About 10% of burn admissions in children are related to child abuse, and about 10% of all child abuse cases include burn injuries.
■ Silicone dressings may help prevent hypertrophic scars in those at risk as well as to improve scar elasticity in already existing symptomatic scars.
■ The most common complication of burns is abnormal or hypertrophic scarring that may cause contractures and impaired function.
Resources
Celis MM, Suman EO, Huang TT, et al. Effect of a supervisedexercise and physiotherapy program on surgical interventions in children with thermal injury. J Burn Care Rehabil. 2003;24:57.
Martin-Herz SP, Patterson DR, Honari S, et al. Pediatric pain control practices of North American burn centers. J Burn Care Rehabil. 2003;24:26.
Mustoe TA, Cooter RD, Gold MH, et al. International clinical recommendations on scar management. Plast Reconstr Surg. 2002;110:560.
O'Brien L, Pandit A. Silicon gel sheeting for preventing and treating hypertrophic and keloid scars. The Cochrane Library. 2007;4.
Sheridan RL, Remensnyder JP, Schnitzer JJ, et al. Current expectations for survival in pediatric burns. Arch Pediatr Adolesc Med. 2000;154:245.
Developmental Conditions
Pearls
■ Observation is the rule in Legg-Calve-Perthes disease, with minimal pain, good ROM, and a strong lateral bony column.
■ Overweight, adolescent, altered gait, and hip pain— think slipped capital femoral epiphysis (SCFE).
■ Typical DDH, if not detected and aggressively treated prior to 18 months, portrays a much higher risk of lifelong disability and degenerative arthritis.
■ If idiopathic toe walking doesn't improve within a few months of aggressive conservative care, a lifelong presentation is likely present.
■ In-toeing in the otherwise able-bodied child generally gets better over time, with or without correction of the bony torsional abnormalities.
Resources
Barch JG: Instructional Course Lectures Pediatrics. Rosemont, IL: American Academy of Orthopedic Surgeons, 2006.
Catterall A. The natural history of Perthes disease. J Bone Joint Surg Br. 1971;53:37-53.
Shipman SA, Helfand M, Moyer VA, et al. Screening for developmental dysplasia of the hip: A systematic literature review for the US preventative services taskforce. Pediatrics. 2006;117(3):E557-E576.
Staheli LT. Fundamentals of Pediatric Orthopedics. 4th ed. Philadelphia, Lippincott, Williams and Wilkins, 2008.
Sutherland DH, Olshen R, Cooper L, et al. The development of mature gait. J Bone Joint Surg Am. 1980;62:336.
Scoliosis
Pearls
■ If pain is associated with scoliosis, check for other etiology, including neoplasm and infection. Scoliosis in children is typically not painful.
■ Steroids reduce the incidence of scoliosis in Duchenne’s muscular dystrophy, as well as delay loss of muscle strength and ambulation.
■ Surgical fusion into the pelvis is generally performed in the nonambulatory child and those with significant pelvic obliquity.
■ Atypical left thoracic curves in individuals with idiopathic scoliosis require investigation for spinal pathology, including MRI imaging.
■ Scoliotic curvatures 50 degrees or greater have a tendency to progress, averaging about a degree per year over a lifetime.
Resources
Dorman J. Pediatric Orthopaedics: Core Knowledge in Orthopedics. 1st ed. Philadelphia, Elsevier Mosby, 2005.
Driscoll SW, Skinner J.
Musculoskeletal complications of neuromuscular disease in children. Phys Med Rehabil Clin N Am. 2008; 19(1);163-94:viii.Larsson E, Normelli H, Oberg B. Long term follow-up of functioning after spinal surgery in patients with neuromuscular scoliosis. Spine. 2005. 30(19):2145-2152.
Murphy N, Firth S, Jorgensen T, Young P. Spinal surgery in children with idiopathic and neuromuscular scoliosis: What’s the difference? J Ped Orthop. 2006;23(2):211-220.
Toree-Healy A, Samdani AF. Newer technologies for the treatment of scoliosis in the growing spine. Neruosurg Clin N Am. 2007;18(4):697-705.
Leg Length Inequality
Pearls
■ Leg length discrepancy of 2 cm or less is common, treated with a shoe lift or observed, depending upon functional preference.
Resources
McCarthy JJ, MacEwen GD. Management of leg length and equality. J South Orthop Assoc. 2001;10(2):73-85; discussion 85.
Constitutional or Intrinsic Bone
Conditions
Pearls
■ Multiple epiphyseal dysplasia and Legg-Calve- Perthes disease both involve the capital femoral epiphysis, but Legg-Calve-Perthes disease is never symmetrical and rarely bilateral.
■ Involvement of the atlantoaxial and atlantooccipital articulations always need to be considered in conditions of constitutional bone.
■ Little people of adult age almost always have normal intellect and psychosocial being requiring treatment as such, despite a physical stature that might suggest otherwise.
■ Macrocephaly in individuals with achondroplasia needs to be followed carefully, including serial head circumferences and surgical referral for symptomatic hydrocephalus.
■ Despite atlantoaxial instability, progressive spasticity, and mental deterioration all common to individuals with a mucopolysaccharidoses syndrome, life expectancy can reach into the fifth decade.
Resources
Barbier O, Allington N, et al. Reflex sympathetic dystrophy in children: review of a clinical series and description of the particularities in children.
Acta Orthop Belg. 1999;65(1):91-97.Baujat G, Legeai-Mallet, et al. Achondroplasia: Best Practice and Research. Clinical Rheumatology. 2008;22(1):3-18.
Danielpour M, Wilcox WR, et al. Dynamic cervi- comedullary cord compression and alterations in cerebrospinal fluid dynamics in children with achondroplasia. J Neurosurg: Pediatrics. 2007;107:504-507.
Horton WA, Hall JG, et al. Achondroplasia. Lancet. 2008;370:162-172.
Newton AW, Vandeven AM. Update on child maltreatment. Curr Opin Pediatr. 2008;20(2):205-212.
Young G, Toretsky JA, et al: Recognition of common childhood malignancies. Am Fam Physician. 2000; 61:2144-2154.
Musculoskeletal Pain and Child Abuse
Pearls
■ Back pain in children, although relatively uncommon, if not improving within a couple weeks of conservative care needs aggressive investigation for potential life-threatening etiologies.
■ Multiple injuries in various stages of healing or those inconsistent with developmental level, blamed on siblings or unwitnessed, should increase suspicion for child abuse.
Resources
Griffin LY. Essentials of Musculoskeletal Care. 3rd ed. Rosemont, IL: American Academy of Orthopedic Surgeons, 2005.
Siambanes D, Martinez JW, Butler EW, et al. Influence of school backpacks on adolescent back pain. J Pediatr Orthop. 2004;24:211-217.
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