Autonomic Agents

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Would a drug that enhanced ciliary body muscle contraction improve accommodation for presbyopes?

No

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Vuity

  • 1.25% pilocarpine

  • FDA approved for the treatment of presbyopia

  • Mechanism of action: parasympathomimetic/cholinergic agonist that binds muscarinic receptors on the sphincter

  • Therapeutic effect: Causes pupillary miosis that increases the depth of focus to improve near visual acuity

  • Dosage: 1 gt BID OU

  • Can also dec. IOP via inc TM outflow

  • Reported ocular side effects:

    • 15% Browache/headache

    • 5% Accommodation inducing distance blur

    • 5% Conjunctival injection

    • Retinal detachment

    • Precautions: exercise caution with night driving

  • Potential Parasympathomimetic Systemic Side Effects:

    • bradycardia

    • bronchoconstriction

    • sweating, salivation

    • Abdominal cramping

  • Ideal Candidates:

    • Age ≤ 50

    • ADD ≤ 2.00 D

    • Emmetropic presbyopes

    • Single vision CL wearers

    • Multifocal CL dropouts/nonadapts

    • Can also be used in addition to multifocal CLs

    • No peripheral retinal disease (do DFE)

  • Supplied in 2.5ml bottle (1 month supply)

  • NO INSURANCE COVERAGE

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Qlosi

  • 0.4% pilocarpine (preservative free)

  • FDA approved for the treatment of presbyopia

  • Mechanism of action: A parasympathomimetic, cholinergic agonist that binds muscarinic receptors on the iris sphincter

  • Therapeutic effect: Causes pupillary miosis that increases the depth of focus to improve near VA

  • Dosage: 1 gt up to BID OU

  • Similar efficacy to Vuity

  • Side effects:

    • Headache 6.8%

    • Sting on instillation 5.8%

    • no retinal detachment risk

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VIZZ

  • 1.44% aceclidine (preservative free)

    • Muscarinic agonist, but more so for M3 on iris

  • FDA approved for the treatment of presbyopia

  • Mechanism of action: A parasympathomimetic, cholinergic agonist that SELECTIVELY binds iris sphincter muscarinic receptors

  • Therapeutic effect: Causes pupillary miosis that increases the depth of focus to improve near VA

  • Dosage: 2 gt QD OU

  • Highest efficacy of FDA presbyopia agents

  • Ocular Side Effects:

    • 20% Instillation irritation

    • 16% Dim vision

    • 13% Headache

    • 8% Conjunctival injection

    • Precautions: exercise caution with night driving

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Upneeq

  • 0.1% oxymetazoline hydrochloride

  • FDA approved for acquired blepharoptosis

  • Mechanism of action: Non-selective alpha adrenergic agonist that contracts Müller’s muscle

  • Therapeutic effect: Increases palpebral fissure by at least 1mm

  • Side effects in 1-5% of patients:

    • Punctate keratitis

    • Instillation irritation, conjunctival hyperemia

    • Blurred vision, headache, dry eye

  • Other potential side effects:

    • sympathomimetic side effects like increased BP

    • Angle closure glaucoma

    • Precautions: narrow angle patients

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Assessing Ptosis

  1. Assess degree of ptosis by measuring Margin Reflex Distance 1 (MRD1)

    1. mm from corneal light reflex to the center of the upper eyelid margin in primary gaze

      1. normal = 4-5mm

      2. A difference of ≥1mm = asymmetry

  2. Confirm diagnosis of benign acquired blepharoptosis by ruling out:

    1. Horner’s syndrome

    2. Myasthenia Gravis

    3. Oculomotor nerve palsy

    4. Chronic progressive external ophthalmoplegia

  3. Trial demonstration

    1. Ask to use patient’s phone to take baseline photo

    2. Instill 1 gt Upneeq OU

    3. Wait 20 minutes

    4. Retake patient photos and document change in MRD1

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