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Br J Ophthalmol 2004;88:1197-1200 doi:10.1136/bjo.2003.029397
  • Clinical science
    • Extended reports

The use of porous polyethylene (Medpor) lower eyelid spacers in lid heightening and stabilisation

  1. J Tan1,
  2. J Olver2,
  3. M Wright3,
  4. R Maini2,
  5. C Neoh1,
  6. A J Dickinson1
  1. 1Royal Victoria Infirmary, Newcastle upon Tyne, UK
  2. 2Western Eye Hospital, London, UK
  3. 3Velindre NHS Trust, Cardiff, UK
  1. Correspondence to: A Jane Dickinson Eye Department, Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne NE1 4LP, UK; Jane.Dickinsonncl.ac.uk
  • Accepted 14 January 2004

Abstract

Background/aims: The management of lower eyelid retraction can be challenging, and established techniques to correct it are not always successful. Previous reports have suggested a role for the ultrathin high density porous polyethylene lower eyelid spacer (Medpor LES) in such patients. The authors report the experience of three surgeons implanting Medpor LES over 1 year, and ascertain whether such implants are a safe and effective alternative to autogenous spacers.

Methods: A prospective, interventional, non-comparative case series of consecutive patients. Surgical indications for Medpor LES were noted. Preoperative and postoperative lower marginal reflex distance (L-MRD), vertical palpebral aperture (PA), lagophthalmos, and scleral show inferior to the limbus (LSS) were recorded, together with major and minor complications.

Results: 32 patients (35 eyelids) had a Medpor LES inserted, 22/32 under local anaesthetic, and nine with adjunctive procedures. Mean follow up was 22 months (range 15–28 months). The Medpor LES was effective in reducing the palpebral aperture (p<0.001) and lagophthalmos (p = 0.04) and raising the lower eyelid height by reducing both L-MRD (p  =  0.006) and LSS (p<0.001). However there were major complications in 7/32 patients and minor complications in 8/32, most requiring further surgery. Final outcome was good in 24/35 eyelids and satisfactory in 5/35.

Conclusions: Despite a good or satisfactory final outcome in the majority of patients, the value of this technique is limited by complications, and should be reserved for those unsuitable for safer techniques.

Footnotes

  • Conflicting interests: none.

  • This paper was presented in part at the meetings of the British Oculoplastic Surgery Society, Manchester, May 2002, and the European Society Ophthalmic Plastic Reconstructive Surgery, Munster, September 2002.

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