Comm Eye Health Vol. 32 No. 105 2019 pp 21-22. Published online 13 May 2019.

Pharmacological interventions in myopia management

Tim Fricke

Senior Research Fellow and Paediatric Optometrist: Brien Holden Vision Institute, Sydney, Australia.

Helena Hurairah

Consultant Ophthalmologist (Paediatrics and Strabismus): Brunei Eye Centre, RIPAS Hospital, Bandar Seri Begawan, Brunei, Darussalam.

Yuqin Huang

Lecturer and Optometrist: Ngee Ann Polytechnic, Singapore.

Suit May Ho

Education Program Manager and Optometrist: Brien Holden Vision Institute, Melbourne, Australia.

Girl putting spectacles on spectacles on while sitting in the classroom
Myopia can get worse very quickly. Drugs such as low-dose atropine can help. CAMBODIA © Dean Saffron, courtesy of Brien Holden Vision Institute Foundation
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Daily low-dose atropine has been shown to result in a reduction of >50% in myopia progression over 3 years – with little to no rebound effect.

The long-term burden of myopia on the health care system, the global economy and individual quality of life requires that we do what we can to avoid or delay myopia onset and, when myopia is present, that we provide optical correction and do our best to slow its progression. Behaviour modifications such as increased time outdoors and reduced near work appear useful in avoiding or at least delaying onset of myopia, but have not been shown to slow progression once myopia is present. There is evidence that optical interventions (p. 19) and the pharmacological options presented here can reduce myopia progression in children. This may reduce the risk of vision impairment later in life from complications such as retinal detachment and myopic macular degeneration.

Daily low-concentration atropine

Atropine is known for its cycloplegic and pupil dilation effects. It cannot correct the blurred vision caused by myopia, but appears to have myopia control effects that are probably mediated in the retina or sclera. This means that doses too small to cause side effects or other symptoms can still reduce myopia progression.

High quality (large cohort, randomised, masked and controlled) trials of 0.01%, 0.025% and 0.05% atropine eye drops have demonstrated significant myopia control effects over 1 year of daily use.1,2

Comparison of the ATOM studies suggests that 0.01% atropine reduces myopia progression (measured as spherical progression) by >50% over 3 years (2 years of use, then 1 of non-use).1 At present, it is less clear to what extent 0.01% atropine reduces myopia progression in terms of axial length. This is an important distinction, because we suspect that axial length is a stronger determinant than spherical equivalent of the lifelong risk of complications such as retinal detachment and myopic macular degeneration. However, further studies are required to confirm this.

With 0.01% atropine, there was little to no rebound effect (i.e., increased myopia progression) during the year of non-use.1 The potential rebound effects of the other low concentrations (0.025% and 0.05%) are not yet known.1,2

Depending on uveal pigmentation and individual sensitivity, all three dosages (0.01%, 0.025% and 0.05%) have subclinical effects on pupil size and accommo-dation, and are therefore very well tolerated.1,2

Low-concentration atropine: unresolved questions

Unsettlingly, we do not know exactly how atropine reduces myopia progression. Atropine has a dose-related effect on accommodation, pupil size, dopamine levels in the retina, and scleral fibroblast activity. Any or all of these mechanisms potentially explain atropine’s myopia progression effect, as this effect also appears to be atropine dose-related, as does post-treatment rebound. However, retinal dopamine levels and/or scleral fibroblast activity appear the most likely candidates.

Low-concentration atropine: the challenges

Low-concentration atropine needs to be compounded in most countries, making it too expensive for many people who would benefit from it. It is also commonly an ‘off-label’ use – meaning reduction in myopia progression was not the reason atropine was approved for use in most countries, which can cause insurance and payment issues. Absence of a local compounding pharmacy can be overcome – compounding pharmacists commonly post or courier drops to patients, even between countries, depending on drug importation rules. The biggest problem remains cost. Pharmaceutical companies have not shown an interest in commercially manufacturing low-concentration atropine because of regulatory hurdles in countries they are most likely to make profits in. This may change if preferred dosage and axial length effectivity questions are resolved.

We have not observed any significant complications from daily low concentrations of atropine, and none have been reported. However, given the potential complications of atropine generally, caution is warranted. Practitioners should note contra-indications (e.g., Down’s Syndrome or spastic paralysis), provide patient information (including critical information about complications), advise sun protection if prescribing concentrations above 0.02%, and advise to return immediately or attend a hospital emergency department if signs of adverse reactions are observed.


Given the current lack of evidence about the potential rebound effect of other concentrations of low-dose atropine, the only treatment regimen we can safely recommend is 0.01% atropine, one drop in each eye once a day (preferably at night, just before bed). We recommend reviewing patients one week after the initiation of atropine use to assess visual function (including distance visual acuity, refraction, accommodation accuracy, and pupil reactions) and to check for any adverse reactions.

After that, it is sensible to regularly review a child with progressive myopia as usual, e.g., every 6–12 months. The practitioner should have clear criteria for ceasing atropine management (e.g., a wash-out period after each 2 years of use, as used in the ATOM studies).2 Various groups are actively investigating the effects of a range of low-concentration atropine regimens on myopia progression. Recommendations may change as future studies are published.

Warning: avoid daily regular-concentration atropine

We do not recommend the use of daily regular-concentration atropine. Although 1% atropine is widely available, and high-quality randomised controlled trials of 0.1%, 0.5% and 1% atropine eye drops have demonstrated strongly significant myopia control effects over 2 years of daily use,1,3 there is a significant rebound effect. One year after ceasing 2 years of daily 1% atropine, study participants showed almost as much cumulative myopia progression as if atropine had never been used.1 Several options for reducing the rebound effect have been proposed (e.g. tapering atropine in either concentration or frequency of use), but none has been shown safe in prospective randomised controlled trials.


Daily, low-concentration atropine appears safe and beneficial, leading to a 59% reduction in myopia progression over 5 years as measured by spherical equivalent refraction. This has the potential to reduce the frequency of high myopia by over 73%6 and reducing the risk of visual impairment associated with higher myopia.

Even so, questions remain about the mechanism of action, efficacy (e.g., does it moderate progression of axial elongation?), the optimal dosage for myopia control, the effect of place and/or ethnicity on optimal dosage, and how atropine interacts with other myopia control interventions (e.g., does combining atropine with dual focus contact lenses or bifocal spectacles result in additive myopia control, does it multiply the effect, or do they interfere with each other?).

We advocate the evidence-based role of daily low-concentration atropine in moderating myopia progression so long as a clear administrative framework, patient safety protocols and drug cessation guidelines are employed.

In our opinion, this currently means considering prescription of 0.01% atropine for use in both eyes, once per day, at night, in appropriate patients.

Other pharmacological candidates


The use of pirenzepine 2% twice a day has been shown to have a significant myopia control effect over 2 years.4 There have been no studies about progression once treatment has stopped, so there is no information about a potential rebound effect. We are unaware of any jurisdictions in which pirenzepine is commercially available.


7-methylxanthine (7-mx) appears to exhibit a safe, significant myopia control effect in both animals and humans.5 As is the case with pirenzepine, there have been no studies about progression once treatment has stopped, so there is no information about a potential rebound effect. Denmark is the only jurisdiction we are aware of in which 7-mx is available and permitted for use.


1 Chia A, Lu QS, Tan D. Five-year clinical trial on Atropine for the Treatment of Myopia 2: Myopia Control with atropine 0.01% eyedrops. Ophthalmol 2016; 123: 391-399.

2 Yam JC, Jiang Y, Tang SM, Law AKP, et al. Low-concentration Atropine for Myopia Progression (LAMP) study: a randomized, double-blinded, placebo-controlled trial of 0.05%, 0.025%, and 0.01% atropine eye drops in myopia control.Ophthalmol 2019; 126: 113-124.

3 Chia A, Chua W-H, Cheung Y-B, Wong W-L, et al. Atropine for the Treatment of Childhood Myopia: safety and efficacy of 0.5%, 0.1%, and 0.01% doses (ATOM2). Ophthalmol 2012; 119: 347-354.

4 Siatkowski RM, Cotter SA, Crockett RS, Miller JM, et al. Two-year multicenter, randomized, double-masked, placebo-controlled, parallel safety and efficacy study of 2% pirenzepine ophthalmic gel in children with myopia. J AAPOS 2008; 12: 332-339.

5 Trier K, Munk Ribel-Madsen S, Cui D, Brogger Christensen S. Systemic 7-methylxanthine in retarding axial eye growth and myopia progression: a 36-month pilot study. J Ocular Biol, Diseases and Informatics 2008; 1: 85-93.

6. Brennan N. Predicted reduction in high myopia for various degrees of myopia control. Contact Lens and Anterior Eye. 2012;35S:14-5.