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BMJ 2007;334:366-368 (17 February), doi:10.1136/bmj.39063.501377.BE
Andrew J Lindford, clinical fellow, Shehan Hettiaratchy, specialist registrar, Fabrizio Schonauer, consultant
Department of Plastic and Reconstructive Surgery, Queen Victoria Hospital, East Grinstead RH19 3DZ
Correspondence to: S Hettiaratchy, Department of Plastic and Reconstructive Surgery, Charing Cross Hospital, London W6 8RF shehan_h{at}hotmail.com
Postpartum splinting can completely correct congenital ear deformities and obviate the need for later surgery
Congenital ear deformities are common and usually corrected surgically in childhood. Ear deformities are often first noticed by parents or non-specialist personnel such as midwives, general practitioners, and health visitors. Splinting of ear deformities in the early neonatal period has been shown to be a safe and effective non-surgical treatment.12345678 The splint is made from a wire core segment in a 6-French silastic tube and held in place with adhesive skin closure strips. It is applied with no anaesthesia for three to four weeks.1 We present three cases that show how different congenital ear deformities can be treated non-surgically, thereby obviating the need for surgery.
Case 1: constricted ear
A male child was born at full term with bilateral constricted ears. No family history of ear deformity existed. In this deformity, the rim of the ear looks as if it has been tightened, rather like a purse string that has been pulled closed.19 We initiated splinting three days after birth and the programme was continued for one month. By 10 days the upper pole had expanded and a good result was seen at six months' follow-up (fig 1
).
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Congenital ear deformities are defined as either malformations (microtia, cryptotia) or deformations. Ear deformation implies a normal chondrocutaneous component with an abnormal architecture.10 Deformed ears are categorised as constricted (fig 1
), Stahl's (fig 2
), or prominent (fig 3
). The causes of these deformities are variable. Abnormal development and functioning of the intrinsic and extrinsic muscles of the ear may generate deforming forces. External forces applied to the ears, such as malpositioning of the head during the prenatal and neonatal periods, may also contribute.10
Although ear deformities are anecdotally common, their true incidence is unknown. Around 5% of the white population are thought to have prominent ears, but this may be an underestimate as most reports do not include less severe anomalies.
Although some of these deformities resolve spontaneously, a large proportion do not. In today's society, which puts great emphasis on appearance, the pressure on parents to seek surgical treatment if their child has an ear deformity can be great.
Several surgical techniques are available to treat these conditions. Although the results are often good, they can be unpredictable, especially for more complex deformities.
Splinting of ears in the early neonatal period has been advocated as an effective non-surgical treatment12345678 that often produces better results than surgery. The best results are achieved and the shortest period of splintage is needed when treatment is started immediately after birth. Moulding of the ears is possible then because maternal oestrogens render the ear of the neonate soft and malleable.45 After the first few days of life the ear becomes stiffer and less amenable to moulding, which makes splinting less effective.
Many kinds of splints and moulding materials have been described (table
). Methods other than the one we used include self adhering foam designed to prevent skin damage from splints,3 temporary stopping (dental material) in combination with surgical tapes,4 dental bite and impression waxes,5 lead-free soldering wire inserted within an 8-French suction catheter, and thermoplastic material.11 Splint kits are now also available from various online sources.
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The potential for splinting congenital ear deformities in early neonatal life needs to be better publicised. Tan and Gault12 reported that parents are the first to notice the deformity at birth in 61% of babies with prominent ears. They should be offered the possibility of splinting to correct these deformities. Postpartum clinical screening and non-surgical treatment are effective for congenital dislocation of the hip joint and congenital club feet. We recommend that similar measures should be taken for congenital ear deformities to obviate the need for surgical correction later in childhood. It is vital that neonatal paediatricians, obstetricians, general practitioners, and midwives are educated about early detection and how to initiate treatment themselves.
The delay incurred by referring to a plastic surgeon may result in a missed opportunity to treat these deformities. If successful, an effective splinting programme could consign the surgical correction of all but the most severe ear deformities to the past.
Competing interests: None declared.
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