Control de la miopía: ahora es el momento ophtalmic & physiological optics 34 (2014)
Ophthalmic & Physiological Optics ISSN 0275-5408
Myopia control: the time is now
For over a century parents have asked clinicians if anything
Refractive development is regulated by visual feedback and
can be done to slow the progression of myopia in their chil-
the process can be manipulated by optical interventions.9,10
dren. Most practitioners shrug their shoulders, add another
Because of the prominence of central vision in primates, it
0.50 DS to the child's prescription and see him or her in
has generally been assumed that signals from the fovea
a year. The tide has now turned. A number of treatments
determine the effects of vision on refractive development,11
have been shown to cut progression rates in half and a
however, experiments in laboratory animals demonstrate
motivated clinician could expand his or her practice to
that ocular growth and emmetropisation are mediated by
incorporate myopia control.
local retinal mechanisms12,13 and that foveal vision is notessential for many vision-dependent aspects of refractivedevelopment.14,15 The peripheral retina, in isolation, can
Optical methods of myopia control
effectively regulate emmetropisation and mediate many of
Progressive addition spectacle lenses (PALs) produce a sta-
the effects of vision on the eye's refractive status.14 More-
tistically significant but clinically irrelevant 11–13% slowing
over, when there are conflicting visual signals between the
of myopia progression based on 2 and 3 year randomized
fovea and the periphery, peripheral vision can dominate
clinical trials.1,2 Other clinical trials of PALs and flat-top
refractive development.16 Collectively, these results suggest
bifocals in hypothetically high-risk groups have found simi-
that optical treatment strategies for myopia that manipulate
larly modest treatment effects.3–5 Larger treatment effects
peripheral vision offer promise.
from spectacle lenses have been reported recently usingexecutive bifocals.6,7 Myopic Chinese Canadian children
Myopia control using peripheral retinal hyperopic
were randomly assigned to one of three treatments: single-
vision lenses, executive bifocals, or executive bifocals withbase-in prism in the near segment of each lens. After
Sankaridurg et al.17 reported the impact of novel spectacle
3 years the treatment effect was 39% and 51% for bifocals
lens designs intended to reduce peripheral hyperopic de-
without and with prism, respectively, although the axial
focus. Myopic Chinese children were randomised to wear-
elongation was similar for each of the two bifocal treatment
ing either one of three novel spectacle lens designs or
groups. The aforementioned studies of multifocal spectacle
conventional, single-vision spectacle lenses for 1 year. For
lenses have been predicated on the hypothesis that myopia
the entire group, no statistically significant reduction in
progression may be slowed by the reduction in accommo-
myopia progression was observed with the novel designs
dative lag by a reading addition. Based on this hypothesis,
although, in children under 12 years with a parental history
one might expect that all multifocal modalities would pro-
of myopia, progression was 30% lower than with control
duce similar effect sizes, but PALs have the smallest effect
spectacles. With spectacles the eye moves behind the lens
and executive bifocals the largest, with flat-top D-segments
and this may diminish the effectiveness of the treatment. If
falling in between. In other words, the larger the near por-
the peripheral hyperopic defocus is manipulated with an
tion, the greater the treatment effect. Taken together, these
optical device whose position remains essentially fixed rela-
studies support an alternative mechanism, that a reduction
tive to the visual axis, greater benefits may be accrued.
in peripheral retinal hyperopic defocus slows myopia pro-
Modern overnight corneal reshaping or orthokeratology
gression and that interventions that reduce peripheral
(Ortho-K) is effective for temporary myopic reduction18
hyperopic defocus should be developed. Indeed, a number
and there was anecdotal evidence that these lenses may slow
of treatments based on this hypothesis have already been
myopia progression in children. Cho et al.19 and Walline
evaluated. These are discussed below, but first the compel-
et al.20 both conducted 2-year case series with historical
ling evidence from animal models of myopia is reviewed.
controls (soft lenses and spectacles, respectively) and foundthat wearing overnight corneal reshaping contact lenses sig-nificantly slowed axial elongation by 46% and 56%, respec-
Evidence for optical methods from animal studies
tively. These preliminary findings were validated by Cho
In his 2010 Prentice Award Lecture at the Annual Meeting
and Cheung21 who reported a 43% treatment effect in a
of the American Academy of Optometry, Earl Smith
2 year randomised clinical trial. Overnight corneal reshap-
reviewed over a decade of careful research demonstrating
ing contact lenses produce a flattening of the central cor-
the viability of optical methods of myopia control.8
nea, leaving the peripheral cornea largely unchanged. One
2014 The Author Ophthalmic & Physiological Optics 2014 The College of Optometrists
Ophthalmic & Physiological Optics 34 (2014) 263–266
effect of this is a change in corneal spherical aberration
myopia.34,36 Time spent outdoors in childhood is not asso-
resulting in foveal vision being corrected to near emmetr-
ciated with rates of myopia progression,37,38 nor does it
opia while the peripheral retina is relatively myopic.22–24
appear to be related to myopia stabilisation.39 A prelimin-
Thus the retardation of myopia progression produced by
ary clinical trial in China has suggested that the incidence
overnight corneal reshaping contact lenses provides seren-
of myopia can be lowered by a program of outdoor activ-
dipitous support for the peripheral hyperopic defocus
ity,37 although, even with incentives, children may be reluc-
tant to persist with such a program.40 Regardless,
Sankaridurg et al.25 reported intriguing results with a
practitioners should encourage parents to have their young
novel contact lens designed specifically to reduce relative
children spend more time outdoors. This can be part of a
peripheral hyperopia. Progression was 34% less than for
broader public health message in the light of increasing
single-vision spectacles. Walline et al.26 recently reported
rates of childhood obesity.
that daily wear distance-centre multifocal soft contactlenses slowed myopia progression by 50% in a 2 year
The future is now
study, although this was with respect to a historicalcontrol group and the reduction in axial elongation was
Readers should anticipate additional evidence on clinical
only 29%. Thus two contact lens modalities, that pro-
myopia control to be forthcoming. Optical therapies will be
duce similar peripheral optical profiles,22 offer promise
refined, particularly for contact lenses, and additional clini-
for myopia control, although practitioners will want to
cal trials will enhance our understanding of the underlying
make their own assessment of the low but finite risks
mechanisms. Given the effectiveness of atropine, commer-
associated with wear.27
cial development of designer myopia drugs has likelystalled, although a sustained release device would be anattractive alternative to daily drug installation.41 Finally,
the mechanism underlying the benefits of outdoor activity
Atropine is probably the most effective treatment to slow
remain unclear42 with Vitamin D,43 light levels and spectral
myopia progression with a mechanism of action that is reti-
composition44 all potentially playing a role. The latter
nal or scleral and not accommodative.28 It is used exten-
could prompt changes in classroom lighting—perhaps rep-
sively in Asian countries, but there has been general
resenting the ocular equivalent of fluoride for teeth. In the
resistance to its widespread adoption in the West given its
meantime, now is the time for clinicians to offer treatment
side effects of cycloplegia and photophobia. A recent clini-
options to their young patients. Depending on your scope
cal trial has demonstrated that the lower concentrations of
of practice, overnight corneal reshaping contact lenses,
0.1% and 0.01% can slow progression by 68% and 59%,
multifocal soft lenses, executive bifocals, or atropine are all
respectively.29 At a concentration of 0.01% accommodation
worthy of consideration. The children deserve something
is relatively unaffected and symptoms absent30 making this
other than an additional
an attractive option that is gaining traction in the US. Theeffect size of low dose atropine is equal or larger than thatreported for selective muscarinic antagonists31 which, com-
bined with the expense associated with drug development,
Portions of this editorial were included in the author's
will likely inhibit the commercialisation of new anti-myo-
George Giles Lecture at the College of Optometrists'
Optometry Tomorrow 2013 conference in Nottingham,UK.
Behavioural approaches
Slowing myopia by changing a child's behaviour has a
dubious history including the SeeClearly Method (http://
In the past 2 years the author has been a consultant for the
en.wikipedia.org/wiki/See_Clearly_Method) and the Bates
following companies who may have an interest in the tech-
Method32 and recent attempts to control myopia by vision
nology discussed: Alcon, Bausch & Lomb, Brien Holden
training have failed.33 Furthermore, in spite of widely held
Vision, and Paragon Vision Sciences.
beliefs that near work causes myopia, several well-designedlarge-scale studies have failed to find a compelling associa-
Mark A. Bullimore
tion between the amount of near work undertaken by a
College of Optometry, University of Houston,
child and the incidence or progression of myopia.34,35 In
contrast, recent studies have found a strong evidence that
E-mail address: [email protected]
more time spent outdoors lowers the risk of developing
2014 The Author Ophthalmic & Physiological Optics 2014 The College of Optometrists
Ophthalmic & Physiological Optics 34 (2014) 263–266
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Mark A. Bullimore
Mark A. Bullimore is an independent regulatory consultant based in Boulder, Colorado. He received his Optometry degreeand PhD in Vision Science from Aston University in Birmingham, England. He was a Professor at The Ohio State UniversityCollege of Optometry for 15 years and taught a number of courses, including geometric optics and ophthalmic optics. Previ-ously, he spent 8 years at the University of California at Berkeley and is currently Adjunct Professor at the University ofHouston College of Optometry. His research interests include myopia, low vision, presbyopia, and refractive surgery. Hereceived grants from the National Institutes of Health to study adult myopia progression.
Mark is an Associate Editor of Ophthalmic and Physiological Optics and the former Editor-in-Chief of Optometry and VisionScience. He is former President and Development Director of the American Optometric Foundation, a philanthropic organi-sation devoted to the advancement of optometric education and research. He served a 4-year term on the U.S. Food andDrug Administration's Ophthalmic Devices Panel and is a consultant for a number of ophthalmic, surgical, and pharmaceu-tical companies.
2014 The Author Ophthalmic & Physiological Optics 2014 The College of Optometrists
Ophthalmic & Physiological Optics 34 (2014) 263–266
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Guido Clemente Solari Montenegro FACTORES DE RIESGO FÍSICO RELACIONADOS CON EL DOLOR LUMBAR: ANALISIS BIBLIOGRÁFICO DE LA SITUACION. PROF. DR. GUIDO C. SOLARI M. ACADEMICO, PROF. ASOCIADO DEPARTAMENTO DE KINESIOLOGIA UNIVERSIDAD DE ANTOFAGASTA 1.- Definición y Clasificación del SDL El lumbago o lumbalgia son términos que permiten hacer referencia al
Ministry of Health and Social Development of the Russian Federation Transfer Factors Use in METHODOLOGICAL LETTER MINISTRY OF HEALTH AND SOCIAL DEVELOPMENT OF THE RUSSIAN FEDERATION Director of Medical Service and the Department of Treatment Developmentfor Health Recovery Resorts (Kurortology) (Signed and Sealed) 30.07.04 No. 14/231 TRANSFER FACTORS USE IN AND SOMATIC DISEASES