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Age and Ageing 2006 35(6):646; doi:10.1093/ageing/afl113
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© The Author 2006. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Drops and falls

SIR—Congratulations on the fascinating case report by Carey highlighting falls caused by ß-blocker eyedrops for glaucoma [1].

We recently saw an 87-year-old man who collapsed in the eye clinic waiting room. He was using twice-daily ß-blocker eyedrops (levobunolol 0.5%) to treat glaucoma complicating corneal graft surgery. An ECG in 2006, before his operation, showed first-degree heart block and a pulse rate of 57 bpm. Several weeks later, he collapsed in the eye outpatient clinic and was unresponsive with a pulse rate of <30 bpm and blood pressure of 100/60 mmHg. ECG showed no acute changes. He recovered after basic resuscitation, and his ß-blocker eyedrops were stopped.

Ten weeks later, his pulse rate had improved to 63 bpm, but he volunteered his satisfaction at not falling over since his change of eyedrops, whereas previously he had daily falls!

Numerous cardiovascular side-effects are attributed to the use of ß-blocker eyedrops including falls, arrhythmia, syncope and myocardial infarction [2]. Glynn et al. found that the commonest cause of falls in elderly glaucoma patients was ß-blocker eyedrops [3].

Systemic absorption of topical ß-blocker eyedrops occurs via the nasal mucosa after passage through the nasolacrimal canal and via pulmonary absorption of inhaled drug particles. These routes avoid hepatic first-pass metabolism giving a high plasma ß-blocker concentration that correlates well with haemodynamic impairment [4]. Vuori and Kaila [5] reported persisting high levels of systemic ß-receptor occupancy 12 h after a single ß-blocker eyedrop; they also noted a slower rate of decline of ß-receptor occupancy in older patients.

Topical ß-blockers need to be considered in any case of falls, and we would like to draw attention to the newer fixed combination eyedrops whose names give no suggestion as to their ß-blocker (0.5% timolol) component (CosoptTM, Combigan®, Xalacom®, DuoTravTM and Ganfort®). Physicians need to specifically ask their patients whether they use eyedrops as many simply fail to recognise them as ‘medication’.

Alexander Spratt*, Lola Ogunbowale, Anthony Khawaja and Wendy Franks

Glaucoma Research Unit, Moorfields Eye Hospital, City Road, London, EC1V 2PD, UK

* To whom correspondence should be addressed at: alexspratt{at}gmail.com

References

  1. Carey B. Atishoo! Atishoo! We all fall down! Age Ageing 2006; 35: 446–7.[Abstract/Free Full Text]
  2. Nelson WL, Fraunfelder FT, Sills JM, Arrowsmith JB, Kitisky JN. Adverse respiratory and cardiovascular events attributed to timolol ophthalmic solution, 1978–85. Am J Ophthalmol 1986; 102: 606–11.[Web of Science][Medline]
  3. Glynn RJ, Seddon JM, Krug JH Jr et al. Falls in elderly patients with glaucoma. Arch Ophthalmol 1991; 109: 205–10.[Abstract/Free Full Text]
  4. Nieminen T, Uusitalo H, Turjanmaa V et al. Association between low plasma levels of ophthalmic timolol and haemodynamics in glaucoma patients. Eur J Clin Pharmacol 2005; 61: 369–74.[CrossRef][Web of Science][Medline]
  5. Vuori M, Kaila T. Plasma kinetics and antagonist activity of topical ocular timolol in elderly patients. Graefe’s Arch Clin Exp Ophthalmol 1995; 223: 131–4.[CrossRef]

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