Published in Ocular Surface

Why Upper Eyelid Meibography is Essential in the Modern Dry Eye Workup

This is editorially independent content
15 min read

Review the basics of meibography and the reasons optometrists should include upper eyelids in meibomian gland evaluations to identify early signs of atrophy.

Image of an optometrist everting the upper eyelid of a patient with meibomian gland dysfunction (MGD).
Dry eye disease (DED) affects more than 18 million US adults, although an estimated 38 million may experience related symptoms.1-3 As one of the most common ocular conditions presenting in clinical practice,4 DED is a multifactorial condition that results in tear film dysfunction that can lead to a vicious cycle of tear hyperosmolarity, cellular apoptosis, inflammation, and injury.5
While there have been major strides in dry eye diagnostic technology—ranging from noninvasive tear breakup time to lipid layer interferometry—one tool has emerged as indispensable: meibography. Yet even as meibography becomes more mainstream, a surprising and persistent oversight remains: most clinicians still only image the glands of the lower lids.
This trend is often driven by workflow challenges rather than clinical rationale, as upper lid eversion is more technically challenging than lower lid eversion. Additionally, many technicians, who are often tasked with obtaining meibography images, may not be as experienced or comfortable manipulating patients' upper eyelids as the doctor.
But skipping upper gland evaluation means you are literally only seeing half the story. As both clinical practice experience and emerging evidence make clear, upper eyelid meibography is essential for accurate diagnosis, early detection, and comprehensive management of DED and meibomian gland dysfunction (MGD).6

Why the meibomian glands matter

Traditionally, dry eye has been separated into three main categories: aqueous-deficient, evaporative, or combined DED, as many cases display elements of both.5 Aqueous-deficient dry eye is caused by a reduction in aqueous production by the lacrimal glands, leading to a low tear volume.
Meanwhile, evaporative dry eye, in which the tear film evaporates prematurely, is considered a major cause of DED and is primarily attributed to MGD, with an estimated prevalence of 51 to 86% among those with DED.5,7-10
Importantly, the TFOS DEWS III report recognizes that evaporative dry eye occurs in at least ~67% of patients with DED and has multiple etiologies, including lid and ocular surface abnormalities.5 Consequently, MGD often plays a central role in the pathophysiology of DED. Of note, it may occur independently or be secondary to the condition itself.
Changes to meibum quality or production—whether from inflammation, obstruction, or gland dropout—create a damaging cycle characterized by altered lipid composition, increased meibum viscosity, bacterial overgrowth, and compromised tear film stability, all of which perpetuate the dry eye cycle and its symptoms.11-13

The importance of meibomian gland assessment

Growing evidence suggests that clinicians may be underdiagnosing, inadequately assessing, or delaying the diagnosis of MGD, as asymptomatic disease is remarkably common.14 Many patients show extensive meibomian gland loss on meibography despite minimal or absent symptoms.14 In fact, asymptomatic MGD occurs more frequently than symptomatic disease.15
However, traditional clinical testing frequently fails to detect early-stage MGD because the body's compensatory mechanisms, particularly increased aqueous tear production and meibomian gland dilation, to maintain tear film stability.16 However, these mechanisms effectively mask the underlying pathology, making early detection difficult with traditional assessments.16
Therefore, direct evaluation of the meibomian glands is vital to early detection of MGD, as changes to gland morphology represent some of the first signs of the disease.6

Performing a thorough MGD evaluation

MGD evaluation starts with assessing gland structure and function. The meibomian gland orifices should be evaluated for signs of obstruction or inflammation.17 Additionally, other eyelid findings such as lash collarettes or telangiectatic vessels should be noted, as they are associated with Demodex blepharitis and ocular rosacea, respectively, and can cause or exacerbate MGD.17
Below are key steps to performing a comprehensive MGD evaluation:
  • Direct visualization of the glands is vital and can be performed either manually or via meibography, however each method begins with eyelid eversion.
  • Manual evaluation of the meibomian glands can be performed by everting the eyelid and then placing a transilluminator against the external aspect of the lid, which allows for visualization of gross gland structure (Figure 1).18-20
  • Infrared meibography (Figure 2) can be used to image the glands in greater detail as it facilitates identification of structural abnormalities, such as gland dropout, tortuosity, and atrophy.6
Figure 1: Meibomian gland transillumination in a patient with MGD.
Meibomian gland transillumination in a patient with MGD.
Figure 1: Courtesy of Cory Lappin, OD, MS, FAAO.
Although meibography has shown to be essential in identifying early MGD and has started to gain wider implementation, it still ranked seventh in popularity among diagnostic tests used in a survey of 215 optometrists.21 The survey found that about 4% always use meibography, 28% use it only in dry eye patients or suspects, and 68% never use it,21 illustrating a gap in the current DED and MGD diagnostic landscape.
When assessing structural changes to the glands, it is essential to look beyond gland dropout. Early-stage disease is often characterized by gland thickening and tortuosity, with gland dropout typically occurring later in the disease process.6,16,22 Therefore, diagnostic approaches that focus primarily on gland dropout to classify and grade the severity of MGD may lead to delayed diagnosis.22
Figure 2: Meibography of upper and lower eyelids in a patient with MGD.
Meibography OU showing meibomian gland obstruction, inflammation, and drop out.
Figure 2: Courtesy of Cory Lappin, OD, MS, FAAO.

Assessing meibomian gland function

Gland function can be assessed through diagnostic gland expression by applying gentle, sustained digital pressure to the eyelid to determine the number of meibomian glands that remain active or expressible.16,23
The clarity of expressed meibum shows meibum quality and distinguishes between healthy glands (which produce clear, easily expressed secretions) and abnormal glands (which produce turbid, thickened oil or opaque, toothpaste-like secretions, such as in Figure 3).16
The Meibomian Gland Evaluator (Johnson & Johnson) can be a helpful tool when assessing meibomian gland function and meibum quality, as the device is calibrated to apply pressure that is equivalent to that of a deliberate physiologic blink, providing a consistent method to evaluate meibomian gland expressibility.42
Additionally, lipid layer interferometry can provide an objective measurement of the tear film’s lipid layer thickness (LLT). A reduction in LLT has been associated with MGD,24,25 and may therefore act as a proxy for meibum production and meibomian gland function.
Figure 3: Toothpaste-like meibum secretion in a patient with MGD.
Toothpaste-like meibum secretion in a patient with MGD.
Figure 3: Courtesy of Cory Lappin, OD, MS, FAAO.

Why upper eyelid meibomian gland evaluation is essential

The common trend of failing to routinely assess the meibomian glands of the upper eyelids in clinical DED and MGD evaluations was spotlighted in a 2025 review by Preeya K. Gupta, MD and Paul Karpecki, OD.6 This review highlighted that the upper glands typically show earlier morphologic changes, including gland tortuosity, dropout, and thickening when compared to the lower glands.6
The upper glands are also longer and slimmer, resulting in greater susceptibility to early structural changes that may precede symptomatic disease, which supports the view that upper lid evaluation is necessary for early disease detection.6
It is also important to note that the structure of the lower glands and upper glands does not always directly correlate, so observation of the lower glands alone cannot be used to make assumptions about the structural status of the upper glands.6
Additionally, the morphological appearance of the upper glands appears to provide critical insight for key patient populations:6
  • Contact lens wearers: Increased meibomian gland tortuosity in the upper lid significantly increases the risk of contact lens dropout, with a 1.74x greater risk.26,27
    • Worsening gland plugging in the upper lids also increases the risk of contact lens dropout, with up to nearly a 5x greater risk depending on severity.26 Additionally, contact lens wearers with worsening upper lid meibum quality are more likely to discontinue lens use due to discomfort.26,27
  • Post-cataract surgery patients: Pre-operative meibomian gland loss of the upper lid significantly predicts post-operative dry eye symptoms, whereas lower lid gland loss may not correlate.28
  • Patients with Sjögren's syndrome (SS): Upper eyelid gland dropout is significantly greater in patients with SS compared to non-SS patients with dry eye.29,30
    • Morphological changes in the upper lid likely contribute to differences in ocular signs and symptoms between SS and non-SS patients.6 These changes may be considered critical for diagnostic purposes.6
  • Thyroid eye disease (TED): Meibomian gland loss of the upper lids is greater in patients with TED than in those with traditional DED.31 This finding may result from factors observed in patients with TED, including incomplete blinking, proptosis, and eyelid retraction.31
    • Patients with TED also have upper glands displaying higher degrees of gland loss with greater central gland dropout than other patients with DED, which correlates with increased ocular surface inflammation and oxidative stress.32 Therefore, assessment of both upper and lower glands can assist in accurately diagnosing TED-related dry eye.6
  • Postmenopausal women with primary acquired nasolacrimal duct obstruction (PANDO): Postmenopausal women with PANDO displayed a greater degree of gland loss in the upper lid along with worse meibum quality compared to the lower glands.33
The upper gland changes observed in these groups demonstrate the vital importance of upper eyelid assessment as part of a comprehensive evaluation of DED and MGD, as its omission can result in missing clinically relevant pathology.

Top tools for meibomian gland evaluation

Modern meibomian gland evaluation increasingly incorporates specialized mechanical tools and artificial intelligence to enhance visualization, consistency, and longitudinal assessment of gland health.

Eyelid everters

Eyelid eversion is necessary for visualizing the meibomian glands whether performed manually with a transilluminator or via meibography, but practicing clinicians and technicians recognize that it can be more challenging to evert the upper eyelids compared to the lowers.34,35 However, the key to obtaining high-quality meibography images is complete lid eversion.
Fortunately, tools now exist to minimize or eliminate the challenges associated with lid eversion. Devices such as the Epstein Lid Everter (Medirix LLC), LidVue Eyelid Everter (VisuScience Meditech), and the Meivertor Everter (Mazado Inc.) make performing lid eversion more efficient, consistent, and successful.
The curved design of the Epstein Lid Everter better fits the contour of the lids, allowing for easier placement and eversion.36 The LidVue Eyelid Everter can help with lower lid eversion by improving handling and patient comfort with its smooth edges.37
The Meivertor was designed to assist in everting both upper and lower lids with a single hand, keeping the other hand free to obtain imaging, all while maintaining patient hygiene and comfort via single-use, disposable silicone tips.38
From a diagnostic standpoint, an important function of meibography is to track gland changes over time, but the appearance of the glands is highly reliant upon consistent lid eversions so comparisons can be made uniformly across images. Therefore, consistent lid eversion is essential because variations in technique significantly alter the meibography image and perceived gland structure.

Tip: The use of lid everters can make lid eversion more uniform resulting in more consistent imaging—and therefore provide more reliable tracking of disease progression.

Artificial intelligence (AI)

Deep learning approaches have shown great promise in automatic image segmentation of meibomian glands for a complete assessment of their morphology. This technology may improve clinicians’ understanding of MGD and enhance diagnostic accuracy.39-41

Takeaways

When conducting a comprehensive dry eye evaluation, meibography should include imaging of both the upper and lower meibomian glands—otherwise, you’re only getting half the story. Meibomian gland dysfunction is now recognized as a leading driver of dry eye disease, particularly in today’s screen-dependent environment.
As a result, diagnostic imaging has become essential to understanding gland structure and identifying early changes. Yet many clinicians still limit their assessment to the lower eyelid glands, often because everting the upper lid can be more technically challenging.
Despite these challenges, evaluating the glands of both eyelids is critical. Early structural changes in MGD frequently appear in the upper glands, and upper lid findings can correlate with a range of clinical conditions—including contact lens discomfort and dropout, post-cataract surgery dry eye, Sjögren’s syndrome, thyroid eye disease, and postmenopausal patients with PANDO.6,33
Fortunately, several tools now help facilitate lid eversion, making upper lid imaging more accessible for both clinicians and technicians.
Bottom line: Comprehensive meibomian gland assessment is essential for early detection and timely intervention. Relying solely on lower lid imaging risks overlooking meaningful early gland changes.6 Therefore, when performing a complete DED and MGD evaluation, imaging the glands of both the upper and lower lids should be considered the standard of care.
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  12. Khanal S, Ngo W, Nichols KK, et al. Human meibum and tear film derived (O-acyl)-omega-hydroxy fatty acids in meibomian gland dysfunction. Ocul Surf. 2021;21:118-128. doi:10.1016/j.jtos.2021.05.009
  13. Nagar S, Ajouz L, Nichols KK, et al. Relationship Between Human Meibum Lipid Composition and the Severity of Meibomian Gland Dysfunction: A Spectroscopic Analysis. Invest Ophthalmol Vis Sci. 2023;64(10):22. doi:10.1167/iovs.64.10.22
  14. Grue JE, Snyder RP, Heinke J. How the Decision to Do (or not do) Meibography Impacts Your Dry Eye Services. Review of Optometric Business. January 15, 2025. Accessed September, 24, 2025. https://reviewob.com/how-the-decision-to-do-or-not-do-meibography-impacts-your-dry-eye-services/.
  15. Viso E, Rodríguez-Ares MT, Abelenda D, et al. Prevalence of asymptomatic and symptomatic meibomian gland dysfunction in the general population of Spain. Invest Ophthalmol Vis Sci. 2012;53(6):2601-2606. Published 2012 May 4. doi:10.1167/iovs.11-9228
  16. Adil MY, Xiao J, Olafsson J, et al. Meibomian Gland Morphology Is a Sensitive Early Indicator of Meibomian Gland Dysfunction. Am J Ophthalmol. 2019;200:16-25. doi:10.1016/j.ajo.2018.12.006
  17. Geerling G, Baudouin C, Aragona P, et al. Emerging strategies for the diagnosis and treatment of meibomian gland dysfunction: Proceedings of the OCEAN group meeting. Ocul Surf. 2017;15(2):179-192. doi:10.1016/j.jtos.2017.01.006
  18. Tomlinson A, Bron AJ, Korb DR, et al. The international workshop on meibomian gland dysfunction: report of the diagnosis subcommittee. Invest Ophthalmol Vis Sci. 2011;52(4):2006-2049. doi:10.1167/iovs.10-6997f
  19. Hom MM. How to perform in-office Meibography. Review of Optometry. July 15, 2002. Accessed September 16, 2023. https://www.reviewofoptometry.com/article/how-to-perform-in-office-meibography.
  20. Fuller D. A better meibomian gland work-up: See what you’ve been missing. Review of Optometry. May 15, 2016. Accessed September 16, 2023. https://www.reviewofoptometry.com/article/a-better-meibomian-gland-workup-see-what-youve-been-missing.
  21. Cole J. Dry eye in optometry: Trends, habits, and hang-ups. Review of Optometry. January 15, 2021. Accessed September 25, 2025. https://www.reviewofoptometry.com/article/dry-eye-in-optometry-trends-habits-and-hangups.
  22. Vunnava KP, Shetty R, Prabhu SM, et al. Automatic segmentation and quantified analysis of meibomian glands from infrared images. Indian J Ophthalmol. 2023;71(4):1426-1431. doi:10.4103/IJO.IJO_2930_22
  23. Chester T, Garg SS, Johnston J, et al. How Can We Best Diagnose Severity Levels of Dry Eye Disease: Current Perspectives. Clin Ophthalmol. 2023;17:1587-1604. Published 2023 Jun 5. doi:10.2147/OPTH.S388289
  24. Finis D, Pischel N, Schrader S, Geerling G. Evaluation of lipid layer thickness measurement of the tear film as a diagnostic tool for Meibomian gland dysfunction. Cornea. 2013;32(12):1549-1553. doi:10.1097/ICO.0b013e3182a7f3e1
  25. Kim WJ, Ahn YJ, Kim MH, et al. Lipid layer thickness decrease due to meibomian gland dysfunction leads to tear film instability and reflex tear secretion. Ann Med. 2022;54(1):893-899. doi:10.1080/07853890.2022.2056238
  26. Pucker AD, Jones-Jordan LA, Marx S, et al. Clinical factors associated with contact lens dropout. Cont Lens Anterior Eye. 2019;42(3):318-324. doi:10.1016/j.clae.2018.12.002
  27. Pucker AD, Jones-Jordan LA, Kunnen CME, et al. Impact of meibomian gland width on successful contact lens use. Cont Lens Anterior Eye. 2019;42(6):646-651. doi:10.1016/j.clae.2019.06.004
  28. Fujimoto H, Ochi S, Inoue Y, Kiryu J. Upper Eyelid Meibomian Gland Dysfunction is a Risk Factor for Dry Eye Symptoms Following Cataract Surgery in the Early Phase. Clin Ophthalmol. 2022;16:293-302. Published 2022 Feb 5. doi:10.2147/OPTH.S346606
  29. Foulks GN, Forstot SL, Donshik PC, et al. Clinical guidelines for management of dry eye associated with Sjögren disease. Ocul Surf. 2015;13(2):118-132. doi:10.1016/j.jtos.2014.12.001
  30. Sullivan DA, Dana R, Sullivan RM, et al. Meibomian Gland Dysfunction in Primary and Secondary Sjögren Syndrome. Ophthalmic Res. 2018;59(4):193-205. doi:10.1159/000487487
  31. Park J, Baek S. Dry eye syndrome in thyroid eye disease patients: The role of increased incomplete blinking and Meibomian gland loss. Acta Ophthalmol. 2019;97(5):e800-e806. doi:10.1111/aos.14000
  32. Inoue S, Kawashima M, Arita R, Kozaki A, Tsubota K. Investigation of Meibomian Gland Function and Dry Eye Disease in Patients with Graves' Ophthalmopathy. J Clin Med. 2020;9(9):2814. Published 2020 Aug 31. doi:10.3390/jcm9092814
  33. Jin H, Chen X, Liu Y. Upper eyelid predominance of meibomian gland dysfunction in postmenopausal women with primary acquired nasolacrimal duct obstruction. BMC Ophthalmol. 2025;25(1):605. Published 2025 Oct 29. doi:10.1186/s12886-025-04439-4
  34. Daniel E, Pistilli M, Ying GS, et al. Association of meibomian gland morphology with symptoms and signs of dry eye disease in the Dry Eye Assessment and Management (DREAM) study. Ocul Surf. 2020;18(4):761-769. doi:10.1016/j.jtos.2020.07.014
  35. Wolffsohn JS, Tahhan M, Vidal-Rohr M, et al. Best technique for upper lid eversion. Cont Lens Anterior Eye. 2019;42(6):666-669. doi:10.1016/j.clae.2019.07.002
  36. Epstein eyelid Everter 2.0. Medirix LLC. Accessed November 26, 2025. https://medirixusa.com/products/epstein-eyelid-everter-2-0.
  37. LidVue. Accessed September 24, 2025. Visuscience.com.
  38. Meivertor. Accessed September 16, 2025. Meivertor.com.
  39. Young K. AI aids analysis of meibomian gland morphology. Primary Care Optometry News. December 2, 2024. Accessed September 25, 2025. https://www.healio.com/news/optometry/20241202/ai-aids-analysis-of-meibomian-gland-morphology.
  40. Setu MAK, Horstmann J, Schmidt S, et al. Deep learning-based automatic meibomian gland segmentation and morphology assessment in infrared meibography. Sci Rep. 2021;11(1):7649. Published 2021 Apr 7. doi:10.1038/s41598-021-87314-8
  41. Wang J, Yeh TN, Chakraborty R, et al. A Deep Learning Approach for Meibomian Gland Atrophy Evaluation in Meibography Images. Transl Vis Sci Technol. 2019;8(6):37. Published 2019 Dec 18. doi:10.1167/tvst.8.6.37
  42. Blackie CA, Korb DR, Knop E, et al. Nonobvious obstructive meibomian gland dysfunction. Cornea. 2010;29(12):1333-1345. doi:10.1097/ICO.0b013e3181d4f366
Cory J. Lappin, OD, MS, FAAO
About Cory J. Lappin, OD, MS, FAAO

Dr. Cory J. Lappin is a native of New Philadelphia, Ohio and received his Bachelor of Science degree from Miami University, graduating Phi Beta Kappa with Honors with Distinction. He earned his Doctor of Optometry degree from The Ohio State University College of Optometry, where he concurrently completed his Master of Science degree in Vision Science. At the college he served as Class President and was a member of Beta Sigma Kappa Honor Society. Following graduation, Dr. Lappin continued his training by completing a residency in Ocular Disease at the renowned Cincinnati Eye Institute in Cincinnati, Ohio.

Dr. Lappin has been recognized for his clinical achievements, receiving the American Academy of Optometry Foundation Practice Excellence award. He has also been actively engaged in research, being selected to take part in the NIH/NEI T35 research training program and receiving the Vincent J. Ellerbrock Memorial Award in recognition of accomplishments in vision science research.

Dr. Lappin practices at Phoenix Eye Care and the Dry Eye Center of Arizona in Phoenix, Arizona, where he treats a wide variety of ocular diseases, with a particular interest in dry eye and ocular surface disease. He is a Fellow of the American Academy of Optometry, a member of the American Optometric Association, and serves on the Board of Directors for the Arizona Optometric Association. He is also a member of the Tear Film and Ocular Surface Society (TFOS) and volunteers with the Special Olympics Opening Eyes program.

Cory J. Lappin, OD, MS, FAAO
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