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Other Eye Conditions

Pregnancy and Eye Diseases (Preeclampsia) (Pregnancy-and-Eye-Diseases-Preeclampsia)

Pregnancy causes widespread physiological effects throughout the body, including an increase in circulating blood volume (approximately 40–50%), dramatic hormonal changes (elevated estrogen, progesterone, and cortisol), and alterations in immune status. These changes directly and indirectly affect the eyes, leading to various ophthalmic events ranging from physiological changes to pathological changes that can threaten life or vision 1).

Ophthalmic changes associated with pregnancy can be broadly divided into reversible physiological changes and pathological changes requiring active intervention.

The main ophthalmic changes related to pregnancy are summarized below.

CategoryMain changes/diseasesNotes
Physiological changesDecreased intraocular pressure (mean 2–3 mmHg)Progesterone enhances aqueous humor outflow
Physiological changesCorneal edema and curvature changesMay cause contact lens intolerance
Physiological changesTemporary myopia and refractive changesOften resolves postpartum
Physiological changesDry eye tendencyTear film instability due to hormonal changes
Pathological changesPregnancy-induced hypertension (preeclampsia)Affects about 3–5% of pregnant women2). Visual symptoms are a serious sign.
Pathological changesWorsening of diabetic retinopathy (DR)Worsens during pregnancy in about 10–30% of patients with pre-existing DR7)
Pathological changesCentral serous chorioretinopathy (CSC)Common in the third trimester; elevated cortisol is involved12)

The decrease in intraocular pressure during pregnancy is a favorable change for glaucoma management, but it also provides an opportunity to review the safety of current eye drops. Refractive surgery (LASIK, ICL, etc.) is contraindicated during pregnancy due to refractive instability and should be considered only after at least 6 months postpartum when refraction has stabilized3).

Q Can vision change during pregnancy?
A

Yes. Hormonal changes can alter corneal shape, lens thickness, and intraocular pressure, causing temporary refractive changes (a tendency toward myopia). Corneal edema or curvature changes may also cause discomfort with contact lenses. These changes often resolve after delivery, but if a change in eyeglass prescription is made due to refractive changes during pregnancy, re-evaluation after delivery is necessary.

Fundus photograph of hypertensive retinopathy in preeclampsia
Fundus photograph of hypertensive retinopathy in preeclampsia
Wood F. Hypertensive retinopathy fundus photograph. Wikimedia Commons. 2009. Figure 1. Source ID: commons.wikimedia.org/wiki/File:Hypertensiveretinopathy.jpg. License: CC BY 3.0.
Fundus photograph of hypertensive retinopathy showing narrowing of retinal arteries, silver-wire arterioles, flame-shaped hemorrhages, and cotton-wool spots (soft exudates). This corresponds to retinal changes due to preeclampsia discussed in section “2. Main Symptoms and Clinical Findings.”

Ocular symptoms during pregnancy vary depending on the underlying disease.

Related to preeclampsia:

  • Blurred vision (haziness)
  • Scintillations (flashing lights) and photopsia
  • Scotomas and visual field defects
  • Transient visual disturbances
  • Accompanying headache and edema (systemic symptoms)

The above visual symptoms are signs of worsening preeclampsia and are risk indicators for eclampsia 6). Prompt consultation with an obstetrician and ophthalmologist is recommended.

During exacerbation of diabetic retinopathy:

CSC (central serous chorioretinopathy) related:

  • Central scotoma and metamorphopsia
  • Decreased vision (usually mild to moderate)
  • Micropsia

Symptoms due to physiological changes:

  • Contact lens discomfort or poor fit
  • Dry eye symptoms (dryness, foreign body sensation, redness)
  • Mild blurred vision (due to corneal edema)

Clinical findings confirmed by the physician

Section titled “Clinical findings confirmed by the physician”

Preeclampsia

Retinal arteriolar changes: Arteriolar narrowing and silver-wire arterioles (evaluated based on the Keith-Wagener-Barker classification).

Hemorrhages and exudates: Flame-shaped hemorrhages and cotton-wool spots (soft exudates).

Elschnig spots: Yellow-white lesions due to choroidal infarction. A sign of poor prognosis.

Serous retinal detachment: Often bilateral. Choroidal ischemia → RPE damage → subretinal fluid accumulation.

Worsening of Diabetic Retinopathy

Increase in microaneurysms: Worsening of existing lesions or new appearance.

Macular edema: Serous or cystoid edema confirmed on OCT.

Neovascularization: Indicates progression from nonproliferative to proliferative DR.

Vitreous hemorrhage: Can cause sudden vision loss due to progression of proliferative DR.

CSC

Serous retinal detachment: Shallow serous retinal detachment localized to the macula.

OCT findings: Subretinal fluid accumulation is clearly visualized.

Fluorescein angiography: Performed only when necessary. Patterns include diffuse or pinpoint leakage.

Cortical Blindness (PRES)

Visual acuity: Transient complete to severe vision loss (bilateral).

Fundus findings: Often normal or only mildly abnormal.

Imaging: MRI/CT shows vasogenic edema in the occipital lobe (coordinate with neurology/obstetrics).

Course: Usually reversible with appropriate blood pressure control and MgSO₄ administration.

Q Is it dangerous to have flickering vision or blurred vision during pregnancy?
A

Flashes of light (photopsia) and blurred vision may be signs of worsening preeclampsia. Especially when accompanied by headache, swelling of the limbs, and elevated blood pressure, there is a risk of progression from preeclampsia to eclampsia (seizures). If these symptoms appear, it is important to immediately consult an obstetrician and also undergo an ophthalmological evaluation.

Optical coherence tomography (OCT) image of central serous chorioretinopathy (CSC) that commonly occurs during pregnancy
Optical coherence tomography (OCT) image of central serous chorioretinopathy (CSC) that commonly occurs during pregnancy
Neches R. Central serous retinopathy OCT scan. Wikimedia Commons. 2010. Figure 1. Source ID: commons.wikimedia.org/wiki/File:Central_serous_retinopathy.jpg. License: CC BY-SA 3.0.
Optical coherence tomography (OCT) shows serous retinal detachment (elevation of the neurosensory retina) and separation from the retinal pigment epithelium (RPE) in the macula. This corresponds to CSC (central serous chorioretinopathy) during pregnancy, discussed in the section “3. Causes and Risk Factors.”

Preeclampsia is a condition characterized by persistent systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg after 20 weeks of gestation 4). The following mechanisms are important in the development of its ocular manifestations.

  • Systemic vascular endothelial damage → spasm and ischemia of retinal arteries
  • Overproduction of anti-angiogenic factors (sFlt-1) → decreased activity of VEGF and PlGF (placental growth factor)
  • Decreased VEGF/PlGF activity → reduced choroidal perfusion → breakdown of the RPE (retinal pigment epithelium) barrier
  • Breakdown of the RPE barrier → fluid accumulation under the retinaserous retinal detachment
  • Vasogenic edema of the occipital lobe → PRES → cortical blindness (reversible) 6)

Risk factors for preeclampsia:

  • Primipara
  • Multiple pregnancy
  • Advanced maternal age (≥35 years)
  • High BMI (25 or higher)
  • History of hypertension, diabetes, or kidney disease
  • History of preeclampsia in a previous pregnancy

Worsening of Diabetic Retinopathy During Pregnancy

Section titled “Worsening of Diabetic Retinopathy During Pregnancy”

Pregnancy is an independent risk factor for progression of diabetic retinopathy (DR), and caution is especially needed in diabetic patients with pre-existing DR 7, 8).

The following mechanisms are involved in the worsening:

  • Increased insulin resistance during pregnancy → amplified blood glucose fluctuations
  • Increased circulating blood volume → increased retinal blood flow → stress on existing microvascular lesions
  • Elevated growth factors (IGF-1, growth hormone, prolactin) → promotion of angiogenesis
  • Rapid improvement in HbA1c → oxygen supply-demand mismatch in retinal ischemic areas → early worsening (transient deterioration) 9)

Risk factors for worsening of DR during pregnancy:

  • Severity of DR before pregnancy (the more severe, the more likely to worsen)
  • High HbA1c before pregnancy
  • Rapid improvement in HbA1c during pregnancy
  • Complication of preeclampsia
  • Type 1 diabetes

CSC (central serous chorioretinopathy) and pregnancy

Section titled “CSC (central serous chorioretinopathy) and pregnancy”

Elevated endogenous cortisol during pregnancy (especially in the third trimester) is thought to increase choroidal vascular permeability and induce CSC. Pregnancy-associated CSC often resolves spontaneously after delivery, but persistent cases can affect vision 12).

Mechanisms of intraocular pressure reduction and corneal changes

Section titled “Mechanisms of intraocular pressure reduction and corneal changes”
  • Progesterone promotes aqueous humor outflow (relaxation of Schlemm’s canal)
  • Decreased episcleral venous pressure due to increased circulating blood volume
  • Corneal edema and curvature changes: water retention in the corneal stroma due to hormonal fluctuations

In ophthalmic evaluation during pregnancy, it is important to select examination methods that consider fetal safety.

Examination methodSafety during pregnancyRecommended scenarios
Dilated fundus examination (tropicamide/phenylephrine)Safe (lacrimal sac compression recommended)Can be performed in all cases. DR: every trimester
OCT (Optical Coherence Tomography)SafeEssential for evaluating serous retinal detachment and macular edema
Intraocular pressure measurementSafeGlaucoma follow-up
Fluorescein angiography (FA)Generally avoided (FDA category C)Only when absolutely necessary. Explain risks and benefits thoroughly
ICG angiographyConsidered contraindicatedAvoid during pregnancy (transfers into breast milk)
Visual field testSafeEvaluation of cortical blindness and optic nerve diseases
Refraction test / corneal topographySafeMonitoring of refractive changes (decision to change correction)

Screening Protocol for Diabetic Retinopathy

Section titled “Screening Protocol for Diabetic Retinopathy”

In pregnant women with diabetes and DR, fundus examination should be performed according to the following schedule:

  • Before pregnancy (when planning pregnancy): Detailed fundus examination. If DR is present, perform laser treatment etc. in advance.
  • Early pregnancy (first trimester): Confirm baseline values.
  • Mid-pregnancy (second trimester): Evaluate for progression of DR.
  • Late pregnancy (third trimester): Final evaluation before delivery.
  • Postpartum: Re-evaluate within 3–6 months after delivery (DR that progressed during pregnancy may improve postpartum) 9)
  • Fundus examination: Evaluation of hypertensive fundus changes according to the Keith-Wagener-Barker classification.
  • OCT: Detection and quantitative evaluation of serous retinal detachment and retinal edema.
  • If cortical blindness is suspected: MRI/CT to confirm occipital lobe edema (coordinate with neurology).
Q Will the dilating drops used for fundus examination during pregnancy affect the baby?
A

Standard doses of mydriatic agents (tropicamide/phenylephrine eye drops) are considered safe for use during pregnancy when administered appropriately. However, it is recommended to minimize systemic absorption by gently pressing the lacrimal sac (inner corner of the eye) after instillation. For pregnant women with diabetic retinopathy, dilated fundus examination is essential to prevent vision loss, and the benefits far outweigh the risks.

The definitive treatment for preeclampsia is delivery (childbirth). Most ocular complications resolve spontaneously after delivery11).

Antihypertensive therapy: The following antihypertensive drugs can be safely used during pregnancy:

  • Methyldopa: Most established safety data. One of the first-line agents.
  • Labetalol: Alpha/beta blocker. Available for intravenous and oral use.
  • Nifedipine (extended-release): Calcium channel blocker. Oral administration.

Contraindicated antihypertensives:

  • ACE inhibitors (captopril, enalapril, etc.): Teratogenic and fetal toxic; contraindicated in pregnancy4).
  • ARBs (candesartan, olmesartan, etc.): Similarly contraindicated in pregnancy.

Management of ocular complications:

  • Serous retinal detachment: Often resolves spontaneously after delivery; additional ophthalmic treatment is usually unnecessary11).
  • Cortical blindness (PRES): Usually reversible with appropriate antihypertensive therapy (target blood pressure: systolic 140–150 mmHg) and MgSO₄ (magnesium sulfate) administration.

Management of Diabetic Retinopathy During Pregnancy

Section titled “Management of Diabetic Retinopathy During Pregnancy”

Pre-pregnancy preparation (planned pregnancy recommended):

  • Reduce HbA1c as much as possible before pregnancy (ideal: HbA1c <6.5%)
  • Complete ophthalmic treatment for pre-existing DR and macular edema before pregnancy
  • If necessary, perform panretinal photocoagulation (PRP) before pregnancy

Treatment strategy during pregnancy:

  • Nonproliferative DR (NPDR): Regular fundus examinations each trimester. Consider photocoagulation if worsening occurs
  • Progression of proliferative DR (PDR): Panretinal photocoagulation (PRP) can be performed during pregnancy. Laser photocoagulation has established safety for the fetus
  • Diabetic macular edema (DME): Anti-VEGF agents are contraindicated during pregnancy (teratogenicity reported in animal studies). Reassess after delivery and initiate anti-VEGF therapy if needed9)
  • Glycemic control: Rapid improvement of HbA1c carries a risk of early worsening. Gradual improvement (decrease of about 0.5–1% per month) is desirable8)

Management of Central Serous Chorioretinopathy (CSC)

Section titled “Management of Central Serous Chorioretinopathy (CSC)”
  • Observation is the basic approach during pregnancy. Most cases resolve spontaneously after delivery
  • For persistent CSC at 3–6 months postpartum, consider photocoagulation (focal photocoagulation to leakage points) or photodynamic therapy (PDT)

Safety of Eye Drops During Pregnancy and Breastfeeding

Section titled “Safety of Eye Drops During Pregnancy and Breastfeeding”

For patients using eye drops (e.g., for glaucoma) who become pregnant or are breastfeeding, safety evaluation of the medication is necessary. The safety classification of major glaucoma eye drops is shown below13, 14).

Drug ClassRepresentative DrugAssessment During PregnancyAssessment During Breastfeeding
Prostaglandin analogsLatanoprost, bimatoprostContraindicated in principle (risk of uterine contractions)Caution
Beta-blockersTimolol, carteololCaution (risk of fetal bradycardia)Caution
Alpha-2 agonistsBrimonidineCaution (risk of central nervous system depression)Contraindicated during breastfeeding (risk of neonatal respiratory depression)
Carbonic anhydrase inhibitors (eye drops)Dorzolamide, brinzolamideCaution (teratogenicity in animal studies)Caution
Artificial tears / hyaluronic acidSodium hyaluronate eye dropsSafeSafe
Tropicamide (mydriatic)Mydrin PSafe (lacrimal sac compression recommended)Safe (lacrimal sac compression recommended)

If continuing beta-blocker eye drops (e.g., timolol), thoroughly perform lacrimal sac compression (press the inner corner of the eye for 1–2 minutes immediately after instillation) to minimize systemic absorption. Brimonidine during breastfeeding carries a risk of central nervous system depression in the newborn and should generally not be used while nursing.

Q Can I continue using glaucoma eye drops during pregnancy?
A

Safety varies greatly by medication. Prostaglandin analogs (e.g., latanoprost) may induce uterine contractions and are generally contraindicated during pregnancy. Beta-blockers (e.g., timolol) require caution for fetal bradycardia but may be continued with thorough lacrimal sac compression in some cases. Once pregnancy is confirmed, always consult your ophthalmologist and obstetrician to consider switching to a safe alternative. Neglecting glaucoma control can also lead to progression of visual field loss, so individualized assessment by a specialist is important.

6. Pathophysiology and detailed mechanisms

Section titled “6. Pathophysiology and detailed mechanisms”
Head MRI FLAIR image of posterior reversible encephalopathy syndrome (PRES) associated with preeclampsia
Head MRI FLAIR image of posterior reversible encephalopathy syndrome (PRES) associated with preeclampsia
Chawla R, Smith D, Marik PE. Near fatal posterior reversible encephalopathy syndrome complicating chronic liver failure. J Med Case Rep. 2009;3:6623. Figure 1. DOI: 10.1186/1752-1947-3-6623. License: CC BY 3.0.
Brain MRI FLAIR image shows multiple subcortical hyperintense areas in the bilateral occipital lobes, parietal lobes, and pons, indicating vasogenic edema due to posterior reversible encephalopathy syndrome (PRES). This corresponds to cortical blindness (PRES) discussed in section “6. Pathophysiology and Detailed Mechanisms.”

Mechanisms of Ocular Involvement in Preeclampsia

Section titled “Mechanisms of Ocular Involvement in Preeclampsia”

Ocular involvement in preeclampsia arises from a complex mechanism based on systemic endothelial dysfunction5, 6).

Excessive production of the anti-angiogenic factor sFlt-1 (soluble Flt-1) from the placenta increases in the circulation, capturing and inactivating VEGF (vascular endothelial growth factor) and PlGF (placental growth factor). This results in systemic endothelial dysfunction, leading to hypertension, proteinuria, and edema.

In the eye, the following cascade occurs:

  • Retinal arteries: Hypertension + endothelial dysfunction → arterial spasm → retinal ischemia → hemorrhage and exudates
  • Choroid: Reduced perfusion → dysfunction of the RPE (retinal pigment epithelium) pump → barrier breakdown
  • RPE barrier breakdown → fluid accumulation under the retinaserous retinal detachment
  • Cerebral vessels: Vasogenic edema in the occipital lobes → PRES (posterior reversible encephalopathy syndrome) → cortical blindness

Cortical blindness due to PRES (posterior reversible encephalopathy syndrome) is a transient, reversible condition resulting from occipital hyperperfusion and blood-brain barrier disruption, and it resolves with appropriate blood pressure control and anticonvulsant therapy.

Mechanisms of Diabetic Retinopathy Worsening During Pregnancy

Section titled “Mechanisms of Diabetic Retinopathy Worsening During Pregnancy”

Worsening of diabetic retinopathy (DR) during pregnancy involves multiple interacting mechanisms. Increased insulin resistance amplifies blood glucose fluctuations, while increased circulating blood volume (approximately 40–50%) raises retinal blood flow, placing stress on existing microvascular lesions7, 8).

Elevations in growth hormone, prolactin, and IGF-1 promote angiogenesis and stimulate VEGF production. Additionally, in patients with poor glycemic control before pregnancy, rapid improvement of HbA1c in early pregnancy can cause a temporary worsening of retinopathy, known as the early worsening phenomenon. This is thought to result from disruption of local oxygen supply-demand balance in retinal ischemic areas due to rapid glycemic improvement8).

Mechanisms of Central Serous Chorioretinopathy (CSC) During Pregnancy

Section titled “Mechanisms of Central Serous Chorioretinopathy (CSC) During Pregnancy”

Elevated endogenous cortisol increases choroidal vascular permeability. Cortisol acts via mineralocorticoid receptors on choroidal endothelial cells, leading to choroidal hyperperfusion and increased vascular permeability → RPE dysfunction → serous retinal detachment12).

Mechanism of intraocular pressure reduction during pregnancy

Section titled “Mechanism of intraocular pressure reduction during pregnancy”

Progesterone relaxes the trabecular meshwork around Schlemm’s canal, reducing intraocular pressure by facilitating aqueous humor outflow. Additionally, hemodilution due to increased circulating blood volume during pregnancy decreases blood viscosity, and changes in episcleral venous pressure also contribute to intraocular pressure reduction. In patients with normal-tension glaucoma, the decrease in intraocular pressure during pregnancy may favorably stabilize symptoms 1).

7. Latest research and future perspectives

Section titled “7. Latest research and future perspectives”

Use of anti-VEGF drugs during pregnancy: Anti-VEGF drugs such as ranibizumab and aflibercept have shown teratogenicity in animal studies and are currently contraindicated during pregnancy. However, there are sporadic case reports of emergency use to prevent vision loss in pregnant women with proliferative diabetic retinopathy or intraocular neovascularization. Systematic data on safety are currently insufficient, and further evidence accumulation is needed 12).

Early prediction using choroidal thickness as a biomarker: Choroidal thickness measured by OCT fluctuates during pregnancy and has been reported to change prior to the onset of preeclampsia. Research is ongoing into the potential of choroidal thickness as an early ophthalmic biomarker for preeclampsia 10).

Correlation between sFlt-1/PlGF ratio and ocular pathology: The sFlt-1/PlGF ratio, which is becoming established as a predictive marker for preeclampsia, is being investigated for its potential correlation with the severity of fundus lesions. Observational studies have shown that cases with high ratios have a higher frequency of serous retinal detachment and Elschnig spots 5).

Standardization of glaucoma management protocols during pregnancy: Glaucoma treatment during pregnancy currently relies on individualized approaches, and there is a need for evidence-based systematic protocols. Selective laser trabeculoplasty (SLT) may be applicable during pregnancy as an alternative to pharmacotherapy, and further investigation is expected 13).


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