U.S. flag

An official website of the United States government

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-.

Cover of StatPearls

StatPearls [Internet].

Show details

Hemianopsia

; ; .

Author Information and Affiliations

Last Update: January 9, 2024.

Continuing Education Activity

Hemianopsia is a clinical term used to describe the disruption of visual pathways within the central nervous system, resulting in the loss of half of the vertical visual field. This condition typically arises due to stroke, brain tumor, or traumatic brain injury. Hemianopsia can be highly disabling, restricting the patient's capacity to navigate their surroundings, read, and operate a vehicle. Consequently, this condition often leads to decreased productivity and increased morbidity due to its impact on the visual pathway. Thus, understanding the functional anatomy of the visual field pathways and correlating visual fields, as well as carefully considering the patient's history and physical examination, can aid in localizing pathological lesions within the central nervous system.

Importantly, it is necessary to remain vigilant for hemianopsia, as both the patient and clinician may overlook the condition. Therefore, it is crucial to maintain a high index of suspicion and consider testing for patients at risk or with neurological findings and visual complaints. Although over half of patients with hemianopsia will experience spontaneous recovery within 1 month following an ischemic stroke, therapies are available to assist patients in adapting and compensating to their environment. Prompt evaluation and accurate diagnosis may identify treatable causes, such as acute ischemic stroke. This activity reviews the etiology, pathophysiology, evaluation, and management of hemianopsia. This activity also equips healthcare professionals with the essential knowledge to treat individuals with hemianopsia and enhance overall patient care.

Objectives:

  • Apply comprehensive knowledge of the functional anatomy of the visual pathway to identify and localize hemianopsia-related lesions accurately.
  • Assess patients presenting with neurological symptoms for potential hemianopsia, recognizing associated findings and promptly initiating a thorough evaluation.
  • Develop a comprehensive understanding of potential abnormalities associated with hemianopsia, facilitating accurate localization and targeted interventions.
  • Communicate effectively with interdisciplinary teams to coordinate comprehensive care for patients with hemianopsia, fostering a collaborative management approach.
Access free multiple choice questions on this topic.

Introduction

Hemianopsia is a clinical term used to describe the disruption of visual pathways within the central nervous system, resulting in the loss of half of the vertical visual field. This condition typically arises due to stroke, brain tumor, or traumatic brain injury. Hemianopsia can be highly disabling, restricting the patient's capacity to navigate their surroundings, read, and operate a vehicle. Consequently, this condition often leads to decreased productivity and increased morbidity due to its impact on the visual pathway. Thus, understanding the functional anatomy of the visual field pathways and correlating visual fields, as well as carefully considering the patient's history and physical examination, can aid in localizing pathological lesions within the central nervous system. 

Visual stimuli are received by each retina and transmitted along the optic nerves to the optic chiasm. Retinal fibers grossly divide into nasal and temporal fibers at the optic chiasm. The nasal fibers decussate, enabling information about the right and left visual fields to separate into their respective pathways for processing on the contralateral side of the brain.[1] For example, the right visual field comprises information from the right nasal and left temporal retinas. After decussation in the optic chiasm, visual information travels along the optic tract through the optic radiations and reaches the ipsilateral primary visual cortex in the occipital lobe. 

Lesions can be classified as prechiasmal, chiasmal, or retrochiasmal. Prechiasmal lesions affect the optic nerve, resulting in monocular blindness in the affected eye.[1] Lesions affecting the optic chiasm disrupt the medial decussating nasal fibers, leading to bitemporal hemianopsia. Lesions located posterior to the chiasm may interfere with the optic tract, optic radiations, or the primary visual cortex. Disruption of the optic tract and primary visual cortex typically results in homonymous hemianopsia, whereas damage to the optic radiations results in an inferior or superior quadrantanopia.[1]

Homonymous hemianopsia, in conjunction with an afferent pupillary defect, indicates the localization of the lesion to the optic tract.[2] The presence of a pupillary defect will be on the side opposite the lesion. This finding is a consequence of damage to the afferent nasal fibers, which cross at the optic chiasm, proceed along the optic tract, synapse on the pretectal nuclei, and subsequently reach the Edinger-Westphal nuclei as part of the afferent pupillary light reflex pathway. Homonymous hemianopsia with preservation of the central visual field, also known as macular sparing, suggests damage to the primary visual cortex. This region receives dual vascular supply from the middle and posterior cerebral arteries.[1]

In summary, it is important to remain vigilant for hemianopsia, as both the patient and clinician may overlook the condition. Therefore, it is crucial to maintain a high index of suspicion and consider testing for patients at risk or with neurological findings and visual complaints. Although over half of patients with hemianopsia will experience spontaneous recovery within 1 month following an ischemic stroke, therapies are available to assist patients in adapting and compensating to their environment. Prompt evaluation and accurate diagnosis may identify treatable causes, such as acute ischemic stroke.

Etiology

Homonymous Hemianopsia

Homonymous hemianopsia refers to a visual field defect that affects either the right or left halves of the visual fields in both eyes. Complete homonymous hemianopsia affects the entire hemifield of both eyes. Such a condition arises with a lesion anywhere along the retrochiasmal visual pathway. The remaining lesions are categorized as incomplete.

Incomplete homonymous hemianopias are further divided into 2 types—congruous and incongruous. Congruous homonymous hemianopia occurs when the homonymous defects in the fields of the 2 eyes are identical in shape, depth, and size. The remaining cases are categorized as incongruous.

Homonymous hemianopsia can result from various causes, including stroke, intracranial hemorrhage, head trauma, mass-occupying lesions, invasive surgical procedures, and neurological conditions such as multiple sclerosis, Alzheimer disease, and epilepsy.[3][4]   

Homonymous hemianopsia is an uncommon symptom caused by severe hyperglycemia.[5] A case presentation reveals homonymous hemianopia in a patient with diabetic ketoacidosis, supported by clinical, laboratory, and radiological findings. However, in such cases, the neurological symptom is transient, with reversible structural changes observed on magnetic resonance imaging (MRI).[6] In addition, seizures may present with hemianopsia in cases such as refractory status epilepticus due to stroke-like migraine attacks after radiation therapy (SMART).[7][8]

Homonymous visual field defects sparing the central 5° to 25° of the visual field on the affected side are frequently observed when the lesion has partially spared the posterior half of the occipital region. Due to the vascular supply of the occipital pole, which often involves branches from both the middle and posterior cerebral arteries, macular-sparing homonymous hemianopia is more prone to occur in strokes compared to other occipital lesions. 

Bitemporal Hemianopsia

Bitemporal hemianopsia is an ocular defect characterized by reduced peripheral vision in the outer temporal halves of the visual field in each eye. Typically, this condition arises from a tumor or lesion affecting the optic chiasm—the point of decussation for the optic nerve—responsible for visual information from the nasal retina in each eye.[9] 

Bitemporal hemianopsia is often associated with mass-occupying lesions such as pituitary adenomas, craniopharyngiomas, and meningiomas.[10] Basilar skull trauma, frontal bone fracture, or vascular lesions, such as anterior communicating artery aneurysms, have also been identified as causes of bitemporal hemianopsia.[11][12][13]

In a case report, a patient is identified with bilateral superior altitudinal hemianopsia (BSAH), where the primary etiology is a pituitary microadenoma leading to inferior optic chiasm damage. The visual field defect observed in the patient includes the macula. Despite the presence of multiple risk factors, including persistent migraine, hypothyroidism, or the potential for ischemic disease affecting the ocular and occipital vessels, imaging did not reveal any evidence of tissue ischemia or infarction that could explain the patient's visual field defects.[14] 

Rare reports of hemianopia exist as a possible adverse effect of vector-based vaccines such as COVID-19.[15] In addition, individuals with a previous history of shaken baby syndrome, when presenting with homonymous hemianopia, exhibit signs of slightly impaired higher visual function, and MRI scans reveal focal damage to the dorsal and ventral reading pathways.[16] 

Binasal Hemianopsia

Binasal hemianopsia is a rare condition that typically occurs in an incomplete form. Potential causes include bilateral internal carotid artery aneurysms, hydrocephalus, intracranial mass lesions, neurosyphilis, and elevated intracranial pressure. 

Epidemiology

The occurrence of hemianopsia varies depending on the underlying pathological condition. In adults, stroke stands out as the predominant cause, accounting for 69.7% of cases, with an average patient age of 58.[3][17] Conversely, in children, neoplasms contribute to 39% of cases, cerebrovascular disease to 25%, and trauma to 19%.[18] An extensive review involving 904 patients with homonymous hemianopsia highlights that stroke primarily affects the occipital lobe in 54% of patients, followed by involvement of the optic radiations in 33% and optic tracts in 6% of patients.

In non-stroke-related homonymous hemianopsia, damage can occur at various locations along the visual pathway. Specifically, 24% affect the occipital lobe, 31% impact the optic radiations, 19% involve the optic tract, and 25% affect multiple locations.[3][19] Pituitary adenomas are the most frequently encountered cause of bitemporal hemianopsia. A systematic review based on radiographic and autopsy studies estimates the overall prevalence of pituitary tumors to be 16.7%.[20] Conversely, occlusive cerebrovascular disease or occipital infarction is identified as the most common cause of homonymous hemianopia with macular sparing.[21]

History and Physical

Patients affected by a visual field defect may not explicitly express their concerns. Instead, they might describe monocular vision loss or a more general sense of visual challenges, such as dimmed vision or difficulty reading. Individuals with visual complaints should undergo a comprehensive physical examination, including a detailed neurological assessment. In cases where neurological emergencies are suspected, characterized by sudden alterations in mental status or the onset of new focal neurological deficits, it becomes crucial to promptly attend to vital signs and initiate immediate management of airway, circulation, and breathing.

A visual acuity test and a comprehensive cranial nerve assessment should be conducted in all individuals to evaluate for visual deficits. The examiner should pay specific attention to pupillary examination and visual field testing. A bitemporal visual field defect helps localize the pathological lesion to the optic chiasm. In contrast, a homonymous visual field defect indicates damage to areas posterior to the optic chiasm, such as the optic tract, optic radiations, or primary visual cortex in the occipital lobe. When an afferent pupillary defect accompanies homonymous hemianopsia, it suggests that the lesion is localized to the optic tract.[2]  

Furthermore, homonymous hemianopsia with macular sparing suggests damage to the primary visual cortex. Macular sparing manifests as preservation of the central visual fields, ranging up to 25°. This finding is crucial as it signifies a posterior cerebral artery occlusion, mitigates the effect of hemianopia, and preserves the ability to read fluently. Two primary theories exist as to why macular sparing occurs.

Dual Representation of the Macula in Each Hemisphere

After the loss of an occipital lobe, the representation in the remaining occipital lobe preserves central vision in the blind hemifield. This phenomenon is supported by midline retinal ganglion cells projecting to the wrong hemisphere. These cells drive neurons in the striate cortex with ipsilateral receptive fields, forming the basis of this theory.[22]

Dual Perfusion Theory

A more widely accepted theory suggests that collateral flow from the middle cerebral artery preserves perfusion in the occipital pole, where the macula is represented, following occlusion of the posterior cerebral artery. Neuroimaging shows preservation of the occipital pole when macular sparing is present.[22]

In addition to severe deficits in their contralesional visual field, individuals with homonymous hemianopsia may demonstrate dissociations between perception and awareness, including:

  • Anosognosia, where patients may lack awareness of their visual field defect.
  • Unconscious visual abilities in the blind hemifield, also known as blindsight.
  • Subtle deficits in the ipsilesional visual field, which the patients may be unaware of.
  • Visual hallucinations, which may occur in the blind field of affected patients. However, the patients may be unaware that their perceptions are unreal.[23]

Evaluation

Testing Visual Fields

Confrontation: Confrontation testing is a simple and valuable method for assessing the visual field. This test is associated with a low sensitivity ranging from 35% to 74%. The below-mentioned steps should be followed to perform this examination.

  • The patient is instructed to sit 1 to 2 feet away from the examiner.
  • The patient is instructed to cover their left eye with their left hand.
  • The patient fixates their right eye to look straight ahead at the examiner's left eye.
  • If the patient does not maintain gaze, the examiner should remind the patient to focus on the examiner's left eye.
  • The examiner closes their right eye.
  • The examiner says, "I will present a moving finger on the edge of your vision and slowly bring it toward the center. As soon as you see movement, say 'yes.'"
  • The presentation of a slowly wiggling finger from the periphery to the center, repeated in each quadrant, provides a sense of the exact location and shape of the visual field.

Formal visual field perimetry: Formal visual field perimetry testing is a crucial method for assessing the visual field with heightened sensitivity as it exceeds the limitations of confrontation testing alone.

  • This testing method involves automated static perimetry and manual kinetic perimetry.
  • This method offers increased sensitivity, providing detailed information about the type, size, and form of visual field loss.
  • This method is considered essential for all patients with neurological lesions causing visual field defects. 

Evaluation of the Underlying Etiology

Neuroimaging combined with physical examination findings can characterize the cause of hemianopsia and guide clinical management. Individuals exhibiting focal neurological findings indicative of a stroke and falling within the intervention window should promptly undergo imaging following institutional protocols or the guidelines outlined by the American Heart Association/American Stroke Association for stroke management.

MRI with contrast of the brain is the preferred method for evaluating both bitemporal hemianopsia and homonymous hemianopsia. When assessing bitemporal hemianopsia, particular emphasis should be placed on examining the optic chiasm and sellar region. In addition, it is crucial to fully examine the retrochiasmal structures, such as the optic tract and occipital lobe, in people with homonymous hemianopsia. Diagnosing homonymous hemianopsia in children can be challenging due to their inability to comply with perimetry. Therefore, children typically undergo an MRI to identify lesions in the retrochiasmatic visual pathway.[24]

Diffusion-weighted imaging is the preferred method for detecting vasogenic edema associated with acute ischemic changes. Notably, in emergent scenarios, computed tomography (CT) may be used to evaluate for ischemia, mass lesions, or vascular aneurysms. In addition, a CT angiogram can be beneficial in large vessel pathologies, such as the middle cerebral artery or posterior cerebral artery occlusion.[25]

 Additional Testing

  • Electroencephalography may be necessary to evaluate the possibility of an underlying seizure disorder.
  • Laboratory testing can evaluate for hyperglycemia and immunoglobulin G4–related disease.
    • Renal function testing may be necessary before administering contrast for imaging studies.
    • Coagulation studies may be required before the administration of thrombolytics in the case of ischemic stroke.
  • A lumbar puncture may be necessary to aid in the diagnosis of multiple sclerosis.

Treatment / Management

The findings from the physical examination and imaging studies should inform clinical management. Patients diagnosed with cerebral infarction or hemorrhage should receive tailored management. Consultation with neurology and neurosurgery is warranted when appropriate. Patients exhibiting mass lesions or signs of increased intracranial pressure may require hospital admission for medical or surgical therapy. 

Patients with visual field deficits may not be aware of the limitations imposed by their condition and might continue to drive. In the United States, each state has unique visual criteria that determine the legal eligibility for driving. The treating clinician is responsible for assessing if the patient meets these legal requirements and providing appropriate counseling on this matter.[26] The American Academy of Ophthalmology summarizes each state's vision requirement. Patient recovery can be enhanced through a comprehensive approach that includes visual training, visual assist devices, occupational therapy, and psychological services.[27] Activity-based interventions, such as visual scanning and compensatory training, have proven to be effective and are commonly utilized in the treatment of hemianopsia.[28]

The objective of rehabilitation is to assist affected patients in adapting to their visual field deficits by enhancing attention and addressing any associated neglect. The techniques used in this process are mentioned below.

Compensation: Patients compensate by relying on their remaining intact function.

Substitution: Patients modify their environment to adapt to their functional limitations.

Restitution: Patients undergo training to redevelop impaired function.

Hemianopic mirrors or prisms can benefit individuals with stroke and homonymous hemianopia as they shift the peripheral image toward the central retinal meridian.[9] Peripheral prisms (p-prisms) expand the visual fields among patients with hemianopsia by shifting images from the blind hemifield onto the intact hemifield, thereby enhancing their ability to navigate hazards in the blind hemifield.[29] However, prisms can cause confusion and spatial distortion in some patients. Although they are suitable for ambulation, it is not advisable to use prisms for driving. 

Individuals experiencing challenges in reading due to homonymous hemianopsia may find it helpful to place a ruler or finger just under the text they are reading. In addition, learning to read vertically can be beneficial for certain individuals. Computerized saccadic training programs are specifically designed to help patients develop the ability to make small saccades or rapid movements into their blind field. The utilization of these programs has demonstrated improvements in reading times and a reduction in scanning errors for some individuals.

Restorative methods aim to broaden the visual field by stimulating the brain adjacent to the blind hemifield. Both animal and human studies suggest that visual-auditory stimulation therapy, leveraging the multisensory architecture of the brain, could effectively restore visual sensitivity in hemianopsia. Recent studies reveal that visual-auditory stimulation therapy may restore visual responsiveness in the neurons of the midbrain indirectly compromised by cortical lesions, leading to the restoration of contralesional space vision.[30] In a recent case study, individuals who underwent visual-auditory stimulation therapy regained the capacity to detect and articulate visual stimuli, determine their location, recognize certain features, and simultaneously perceive multiple visual stimuli in both fields. Multisensory therapy is a potentially fast and effective way to restore visual function in patients with hemianopia.[31][32] Some researchers suggest that the improvement is more likely associated with increased attention directed toward the edge of the blind field rather than an actual expansion of the visual field.

Biofeedback training effectively improves visual function and enhances the quality of life for individuals with homonymous hemianopia.[33] This therapy enhances oculomotor control and repositions the visual fields by altering the patient's fixation point. The improvements attributed to biofeedback therapy include enhanced visual acuity for distance and near vision, improved contrast sensitivity, increased retinal sensitivity, and enhanced reading speed.

Differential Diagnosis

The differential diagnosis of hemianopsia relates closely to the location and the underlying etiology. The following list contains the differential diagnoses for hemianopsia:

  • Cerebral infarction
  • Intracranial hemorrhage
  • Saccular aneurysm
  • Mass lesions, including primary and metastatic tumors
  • Pituitary adenoma
  • Craniopharyngioma
  • Meningioma
  • Central nervous system lymphoma or other primary malignancy
  • Altitudinal hemianopia
  • Trauma
  • Inflammatory conditions, including demyelinating disorders
  • Severe hyperglycemia
  • Degenerative neurological conditions 
  • Migraine
  • Transient ischemia attack
  • Seizure or status epilepticus [34]
  • Immunoglobulin G4–related disease [35]

Prognosis

Visual loss in the setting of stroke suggests a poor prognosis, with the rate of improvement ranging widely from 17% to 67%. Certain studies indicate that only 18% of patients with homonymous hemianopsia regain their vision within 28 to 30 days of the inciting event. In contrast, others report spontaneous improvement in 46% to 67% of cases within 1 month of an ischemic stroke.[36][37][38] The chances of visual recovery diminish over time, with the likelihood of regaining visual function notably low after 6 months.[27][39] 

Patients with bitemporal hemianopsia attributed to pituitary tumors typically experience visual field improvement in 79% to 95% of cases following resection. However, the extent of recovery may hinge on factors such as retinal nerve fiber layer thickness, preoperative deficit severity, duration of visual symptoms, tumor size, extent of resection, and patient age.[40]

A recent study explores the adaptation process of patients to post-stroke hemianopsia visual field loss by closely monitoring early-stage adaptation. The results highlight that adaptation to hemianopsia is individualized and influenced by factors such as the outcomes of a mobility assessment course (MAC) and the degree of inferior visual field loss. The authors recommend incorporating MAC as an assessment tool for evaluating mobility and scanning during rehabilitating patients with homonymous hemianopsia.[41][42]

Complications

Complications associated with hemianopsia, including impaired balance, heightened risk of falls and injury, loss of independence, reading difficulties, impaired visual scanning, increased risk of depression, and reduced employment opportunities, can significantly impact the quality of life in patients.

Deterrence and Patient Education

Hemianopsia refers to the loss of half of a visual field, with stroke being the most common cause in adults, followed by brain tumors and traumatic brain injury. In children, brain tumors are the leading cause. Hemianopsia can often go unnoticed by both clinicians and patients. Any patient presenting with neurological symptoms and reporting decreased visual acuity or difficulties reading should undergo formal visual field testing. This condition can significantly impact daily life by restricting activities such as reading and driving, and increasing the risk of injury, falls, and depression.

Spontaneous recovery occurs in over 50% of patients within the first month following an ischemic stroke. Treatment options focus on compensation and adapting to their environment. Experts continue to debate the effectiveness of restorative therapy.

Patients should receive education on reducing risk factors for stroke, including hypertension, diabetes, hyperlipidemia, vascular disease, and smoking. Assessing the patient's ability to drive is crucial. Due to potential limitations in employment and leisure activities, screening for depression is also essential.

Enhancing Healthcare Team Outcomes

Hemianopsia is a debilitating condition that causes affected patients to encounter challenges in navigating their environment and performing essential tasks such as reading, writing, and driving. The visual impairment places them at risk of losing independence and experiencing falls, injuries, depression, and employment issues. This condition often causes reduced productivity and increased morbidity in patients due to its impact on the visual pathway, underscoring the need for increased clinician awareness and knowledge to facilitate prompt evaluation and treatment. Accurately diagnosing and effectively managing hemianopsia is crucial for improving a patient's quality of life. This requires a collaborative approach that ensures patient-centered care, which can positively impact their long-term physical and mental well-being.

Both patients and healthcare professionals may overlook visual field defects. All clinicians involved in the care of these patients, including primary care, neurology, endocrinology, ophthalmology, neurosurgery, and physical and occupational therapy, must have the necessary clinical knowledge to identify and diagnose hemianopsia. This knowledge includes recognizing patients at risk for developing hemianopsia and understanding appropriate visual field testing techniques. Visual field testing is an essential tool for clinicians to formulate appropriate treatment strategies, contributing to better patient outcomes. Therefore, it is also crucial for clinicians to proficiently and accurately interpret visual field testing results to identify lesion localization within the central nervous system.

Clinicians should exercise vigilance in identifying hemianopsia and perform a thorough evaluation to detect potential abnormalities. Recognizing the urgency of the situation, clinicians should initiate immediate neuroimaging and consultation to pinpoint and address the underlying cause in affected patients. Patients dealing with visual field deficits may endure depression and anxiety. Social and psychological support play crucial and integral roles within the healthcare team.[27] Efficient interprofessional communication is crucial for fostering collaborative decision-making among team members. This coordination enhances patient safety, reduces morbidity, and improves overall quality of life for patients experiencing hemianopsia.      

Review Questions

References

1.
Swienton DJ, Thomas AG. The visual pathway--functional anatomy and pathology. Semin Ultrasound CT MR. 2014 Oct;35(5):487-503. [PubMed: 25217301]
2.
Mehra D, Moshirfar M. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Jul 24, 2023. Neuroanatomy, Optic Tract. [PubMed: 31751030]
3.
Zhang X, Kedar S, Lynn MJ, Newman NJ, Biousse V. Homonymous hemianopia in stroke. J Neuroophthalmol. 2006 Sep;26(3):180-3. [PubMed: 16966935]
4.
Zhang X, Kedar S, Lynn MJ, Newman NJ, Biousse V. Homonymous hemianopias: clinical-anatomic correlations in 904 cases. Neurology. 2006 Mar 28;66(6):906-10. [PubMed: 16567710]
5.
Xiang XH, Fang JJ, Yang M, Zhao GH. Hyperglycemic hemianopia: A case report. World J Clin Cases. 2021 Mar 06;9(7):1720-1727. [PMC free article: PMC7942036] [PubMed: 33728317]
6.
Chukwudelunzu FE, Fugoso L. Diabetic Ketoacidosis Causing Transient Homonymous Hemianopia and Generalized Seizure: A Case Report and Literature Review. WMJ. 2023 May;122(2):127-130. [PubMed: 37141479]
7.
de Oliveira Franco Á, Anzolin E, Schneider Medeiros M, Machado Castilhos R, Targa Martins R, Moser Filho HL. SMART Syndrome Identification and Successful Treatment. Case Rep Neurol. 2021 Jan-Apr;13(1):40-45. [PMC free article: PMC7879299] [PubMed: 33613243]
8.
Jaraba S, Puig O, Miró J, Velasco R, Castañer S, Rodríguez L, Izquierdo C, Simó M, Veciana M, Falip M. Refractory status epilepticus due to SMART syndrome. Epilepsy Behav. 2015 Aug;49:189-92. [PubMed: 26071996]
9.
Kaur K, Gurnani B. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Jun 11, 2023. Fresnel Prisms. [PubMed: 36943983]
10.
Ntali G, Wass JA. Epidemiology, clinical presentation and diagnosis of non-functioning pituitary adenomas. Pituitary. 2018 Apr;21(2):111-118. [PubMed: 29368293]
11.
Ahmad Fauzi S, Nor Sharina Y, Ibrahim M. Isolated Traumatic Bitemporal Hemianopia. Cureus. 2021 Aug;13(8):e17593. [PMC free article: PMC8483391] [PubMed: 34646645]
12.
Vellayan Mookan L, Thomas PA, Harwani AA. Traumatic chiasmal syndrome: A meta-analysis. Am J Ophthalmol Case Rep. 2018 Mar;9:119-123. [PMC free article: PMC5861742] [PubMed: 29577103]
13.
Yoshihara MK, Lui F. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Aug 7, 2023. Neuroanatomy, Bitemporal Hemianopsia. [PubMed: 31424797]
14.
Anbar F, Lerebours V, Shaikh S. Bilateral Superior Altitudinal Hemianopsia with Macular Involvement Confirmed by Multifocal Visual Evoked Potential Testing. Cureus. 2019 Feb 27;11(2):e4149. [PMC free article: PMC6488337] [PubMed: 31058032]
15.
Allahyari F, Molaee H, Hosseini Nejad J. Covid-19 vaccines and neurological complications: a systematic review. Z Naturforsch C J Biosci. 2023 Jan 27;78(1-2):1-8. [PubMed: 36087300]
16.
Bevilacqua L, Kuczynski A, James-Galton M, Leff AP. An inability to learn to read caused by shaken baby syndrome. BMJ Case Rep. 2014 Apr 28;2014 [PMC free article: PMC4009851] [PubMed: 24777081]
17.
SMITH JL. Homonymous hemianopia. A review of one hundred cases. Am J Ophthalmol. 1962 Oct;54:616-23. [PubMed: 13989472]
18.
Liu GT, Galetta SL. Homonymous hemifield loss in childhood. Neurology. 1997 Dec;49(6):1748-9. [PubMed: 9409388]
19.
Bowman R, Walters B, Smith V, Prise KL, Handley SE, Green K, Mankad K, O'Hare P, Dahl C, Jorgensen M, Opocher E, Hargrave D, Thompson DA. Visual outcomes and predictors in optic pathway glioma: a single centre study. Eye (Lond). 2023 Apr;37(6):1178-1183. [PMC free article: PMC10101957] [PubMed: 35562551]
20.
Ezzat S, Asa SL, Couldwell WT, Barr CE, Dodge WE, Vance ML, McCutcheon IE. The prevalence of pituitary adenomas: a systematic review. Cancer. 2004 Aug 01;101(3):613-9. [PubMed: 15274075]
21.
Shin HY, Kim SH, Lee MY, Kim SY, Lee YC. Late emergence of macular sparing in a stroke patient: Clinical Case Report. Medicine (Baltimore). 2017 Jul;96(29):e7567. [PMC free article: PMC5521927] [PubMed: 28723787]
22.
Horton JC, Economides JR, Adams DL. The Mechanism of Macular Sparing. Annu Rev Vis Sci. 2021 Sep 15;7:155-179. [PMC free article: PMC8638601] [PubMed: 33979527]
23.
Misawa M, Pyatova Y, Sen A, Markowitz M, Markowitz SN, Reber M, Daibert-Nido M. Innovative vision rehabilitation method for hemianopsia: Comparing pre- and post audio-luminous biofeedback training for ocular motility improving visual functions and quality of life. Front Neurol. 2023;14:1151736. [PMC free article: PMC10126773] [PubMed: 37114220]
24.
Haaga M, Trauzettel-Klosinski S, Krumm A, Küster S, Ivanov I, Cordey A, Gehrlich C, Staudt M. Homonymous Hemianopia in Children and Adolescents: An MRI Study. Neuropediatrics. 2018 Apr;49(2):142-149. [PubMed: 29351692]
25.
Costello FE, Goyal M. Neuroimaging in neuro-ophthalmology. Neurol Clin. 2010 Aug;28(3):757-87. [PubMed: 20637999]
26.
Gilhotra JS, Mitchell P, Healey PR, Cumming RG, Currie J. Homonymous visual field defects and stroke in an older population. Stroke. 2002 Oct;33(10):2417-20. [PubMed: 12364731]
27.
Goodwin D. Homonymous hemianopia: challenges and solutions. Clin Ophthalmol. 2014;8:1919-27. [PMC free article: PMC4181645] [PubMed: 25284978]
28.
Liu KPY, Hanly J, Fahey P, Fong SSM, Bye R. A Systematic Review and Meta-Analysis of Rehabilitative Interventions for Unilateral Spatial Neglect and Hemianopia Poststroke From 2006 Through 2016. Arch Phys Med Rehabil. 2019 May;100(5):956-979. [PubMed: 31030733]
29.
Houston KE, Peli E, Luo G, Bowers AR, Woods RL. Effects of Perceptual-motor Training on Collision Judgments with Peripheral Prism Expanded Vision. Optom Vis Sci. 2022 Dec 01;99(12):875-884. [PubMed: 36594755]
30.
Dakos AS, Jiang H, Stein BE, Rowland BA. Using the Principles of Multisensory Integration to Reverse Hemianopia. Cereb Cortex. 2020 Apr 14;30(4):2030-2041. [PMC free article: PMC7175010] [PubMed: 31799618]
31.
Rowland BA, Bushnell CD, Duncan PW, Stein BE. Ameliorating Hemianopia with Multisensory Training. J Neurosci. 2023 Feb 08;43(6):1018-1026. [PMC free article: PMC9908311] [PubMed: 36604169]
32.
Jiang H, Rowland BA, Stein BE. Reversing Hemianopia by Multisensory Training Under Anesthesia. Front Syst Neurosci. 2020;14:4. [PMC free article: PMC7006460] [PubMed: 32076401]
33.
Chokron S, Dubourg L, Garric C, Martinelli F, Perez C. Dissociations between perception and awareness in hemianopia. Restor Neurol Neurosci. 2020;38(3):189-201. [PubMed: 31929128]
34.
Lawson J, Triner W, Kluge B. Occipital Lobe Status Epilepticus, A Stroke Mimic with Novel Imaging Findings: A Case Report. Clin Pract Cases Emerg Med. 2022 Aug;6(3):212-215. [PMC free article: PMC9436493] [PubMed: 36049189]
35.
Kohno S, Tabuchi H, Fukushima A. A Case of Immunoglobulin G4-Related Ophthalmic Disease With Unilateral Visual Field Impairment. Cureus. 2022 Jul;14(7):e27495. [PMC free article: PMC9424796] [PubMed: 36060322]
36.
Bruce BB, Zhang X, Kedar S, Newman NJ, Biousse V. Traumatic homonymous hemianopia. J Neurol Neurosurg Psychiatry. 2006 Aug;77(8):986-8. [PMC free article: PMC2077612] [PubMed: 16574725]
37.
Gray CS, French JM, Bates D, Cartlidge NE, Venables GS, James OF. Recovery of visual fields in acute stroke: homonymous hemianopia associated with adverse prognosis. Age Ageing. 1989 Nov;18(6):419-21. [PubMed: 2629493]
38.
Parisi JL, Bell RA, Yassein H. Homonymous hemianopic field defects and driving in Canada. Can J Ophthalmol. 1991 Aug;26(5):252-6. [PubMed: 1933663]
39.
Ali M, Hazelton C, Lyden P, Pollock A, Brady M., VISTA Collaboration. Recovery from poststroke visual impairment: evidence from a clinical trials resource. Neurorehabil Neural Repair. 2013 Feb;27(2):133-41. [PubMed: 22961263]
40.
Uy B, Wilson B, Kim WJ, Prashant G, Bergsneider M. Visual Outcomes After Pituitary Surgery. Neurosurg Clin N Am. 2019 Oct;30(4):483-489. [PubMed: 31471055]
41.
Howard C, Czanner G, Helliwell B, Rowe FJ. Adaptation to post-stroke homonymous hemianopia - a prospective longitudinal cohort study to identify predictive factors of the adaptation process. Disabil Rehabil. 2022 Sep;44(18):5152-5161. [PubMed: 34053393]
42.
Howard C, Currie J, Rowe FJ. UK exceptional case driving application outcomes in post-stroke homonymous hemianopia: results from a clinical study. Disabil Rehabil. 2023 Dec;45(24):4065-4073. [PubMed: 36377421]

Disclosure: Jonah Ruddy declares no relevant financial relationships with ineligible companies.

Disclosure: Ria Monica Asuncion declares no relevant financial relationships with ineligible companies.

Disclosure: Alfonso Cardenas declares no relevant financial relationships with ineligible companies.

Copyright © 2024, StatPearls Publishing LLC.

This book is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ), which permits others to distribute the work, provided that the article is not altered or used commercially. You are not required to obtain permission to distribute this article, provided that you credit the author and journal.

Bookshelf ID: NBK562262PMID: 32965933

Views

  • PubReader
  • Print View
  • Cite this Page

Related information

  • PMC
    PubMed Central citations
  • PubMed
    Links to PubMed

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...