FormalPara Key Summary Points

Most of the existing commercial devices are useful for managing MGD if performed correctly.

Regular therapeutic sessions of eyelid hygiene are required to maintain the improvement in MGD after the initial one.

Several studies have showed that thermal pulsation and intense pulsed light can be the most efficient therapies in the medium and long term.

Clinicians should counsel patients based on MGD severity and treatment compliance.

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Introduction

Meibomian gland dysfunction (MGD) is a chronic, diffuse abnormality of the meibomian glands (MG), characterized by terminal duct obstruction and changes in the glandular secretion. This anomaly may result in alterations of the tear film, symptoms of eye irritation, clinical inflammation, and ocular surface disease [1]. Its prevalence varies between 3.5% and 19.9% in the Caucasian population, while it reaches > 60% in the Asian population [2].

MGs are sebaceous glands located in the tarsal plates of the eyelids, and their function is to release lipids and proteins to the tear film [3]. The crucial role of the MG secretion, also called meibum, is the stabilization of the tear film and the protection of the ocular surface [4, 5].

According to the ‘International Workshop on Meibomian Gland Dysfunction’ [1], MGD is classified into two categories based on the meibum: low-delivery and high-delivery states. Low-delivery states are further divided into hyposecretory and obstructive conditions, the obstructive being the most prevalent type. Obstructive MGD is characterized by chemical changes in the meibum or terminal duct obstruction. Hyposecretory MGD is defined by a reduced release of meibum without MG obstruction. A high-delivery state or hypersecretory MGD is characterized by the presence of a large volume of lipids on the lid margin [1].

MGD is the main cause of evaporative dry eye disease (DED), the most prevalent type of DED. Additionally, MGD is present in some cases of aqueous-deficiency DED [2]. DED is an ocular surface anomaly whose prevalence ranges from 5 to 50% worldwide, and it is associated with limitations in performing activities of daily life and even sometimes with depression [6, 7]. Therefore, it is important to properly manage MGD.

Some therapies for MGD include improving the environmental humidity, increasing dietary omega-3 fatty acid intake, using artificial tears, or anti-inflammatory therapy for DED. Nevertheless, since the final goal of the treatment is to improve the flow of MG secretions [8], eyelid hygiene is the most common clinical treatment. It consists of the application of heat and a mechanical massage of the eyelids to increase meibum secretion [1]. However, traditional warm compresses need to be reheated approximately every 2 min to maintain the heat for a sufficient period of time (usually 10 min). This limitation makes it a time-consuming therapy and hampers compliance, which result in a lack of effectiveness [9, 10]. Considering that there is no standard recommendation for eyelid warming and it must be easily performed to increase compliance, new therapies designed for MGD management are emerging on the market.

This review aims to detail the latest commercial medical devices available for MGD management and their clinical effectiveness. In addition, each study included in this review addressing the effectiveness of any therapy has been classified in terms of level of evidence following the Scottish Intercollegiate Guideline Network (SIGN) [11]. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

Warming Eyelid Devices

Warming Devices

Warming masks help to release the meibum secretion through their application on the closed eyelids. The physiological melting point of the meibum is 32 °C, but in patients with MGD, it is reported to increase up to 45 °C because of the alteration of its chemical composition [12]. Due to the increased melting point, temperatures close to 45 °C have been advocated for warm compress therapy [10]. Skin burns have been reported to occur after 35 min of continuous exposure to thermal contact of 45 °C [13, 14]. Therefore, eye care practitioners usually recommend using warming devices for 5–10 min, preventing adverse effects [15].

The MGDRx EyeBag® (The Eyebag Company, Halifax, UK) is a reusable silk and cotton mask that can be heated in a microwave for 40 s. Peak temperatures (37.6 °C) may be reached after 2 min of its application on the external upper eyelids. After 12 min of treatment, temperatures may slightly decrease (36.8 °C) [16, 17].

Bilkhu et al. [17] (level of evidence: II) observed that 5 min of the MGDRx EyeBag® application twice a day for 2 weeks was an effective and safe treatment for MGD. Moreover, the benefits could last for 6 months when subjects continued the therapy occasionally. Murphy et al. [18] (I) showed that increasing the treatment time to 10 min seemed to be equally effective. However, Ngo et al. [19] (I) found no significant changes in clinical signs after 1 month using the MGDRx EyeBag® twice a day for 10 min.

The EyeBag® Instant (The Eyebag Company, Halifax, UK) is a single-use, disposable warm compress. It is activated by air; therefore, it starts to heat 2–3 min after the mask is removed from the sachet, and it can be placed on the eyelids for 10 min [20].

The eyeXpress™ Eye Hydration System (Holbar Medical Products, USA) is a goggle system, which provides constant but adjustable heat to the anterior surface of both eyelids. It can be applied for 15 min in the required number of sessions [21].

The TearCare® System (Sight Sciences, USA) is an electrothermal controller that heats both eyelids to 41–45 °C by adjusting them with a flexible, single-use material called iLid™. The system encourages meibum expression through normal blinking during the treatment and through the subsequent manual MG expression—the set includes a disposable EXPRESS™ Forceps to perform the manoeuvre. Badawi et al. [22, 23] performed a clinical trial (I) evaluating the effectiveness of the TearCare® System and the MGDRx EyeBag® in two different groups of MGD patients. While one group underwent the TearCare® for 12 min and subsequent MG expression, the other group self-applied 5 min of daily therapy with EyeBag® for 4 weeks. The TearCare® group showed a higher improvement in signs, including MG scores, and symptoms. Additionally, the effects lasted for 6 months, and no adverse events were reported.

The MiBo Thermoflo® (Mibo Medical Group, USA) consists of a tactile power console and a wired metal eye pad. The eye pad is heated (temperature not reported) and applied on the closed eyelids along with an ultrasound gel. There is only one case report (III) indicating that an increase in the temperature of the inner surface of the eyelids was not found after 12 min of the MiBoFlo eye pad application [24]. Therefore, further studies to prove the effectiveness of this device are required.

The EyeGiene® Insta-Warmth System™ (Eyedetec Medical, USA) works by placing the Warming Wafers inside the mask, without heating them in the microwave. It produces heat from a chemical reaction in each wafer. Some studies compared this device with the MGDRx EyeBag®. Wang et al. [25] (I) showed that clinical signs improved after the application of both therapies. Both treatments transferred their peak temperatures to the eyelids in 3 min, although they were slightly lower in the EyeGiene® than in the EyeBag®. Furthermore, Wang et al. [26] (III) found that the warming effect of the EyeBag® was more prolonged. Therefore, the EyeBag® would be more effective for severe cases of MGD.

Warming and Humidity Devices

These devices also soften the meibum to increase its release by applying moist heat to the eyelids. Although it remains unclear, it was hypothesized that moist warming devices might be less effective than dry warming devices because of the cooling that follows the rapid heat evaporation in the case of moist devices [27].

The BRUDER Moist Heat Eye Compress (Bruder Healthcare, USA) is a reusable mask that absorbs water molecules from the air and releases them as moist heat. The device might maintain 54 °C during the first 3 min, and this temperature may slowly decrease, reaching 45 °C after 12 min. The contact of this high temperature mask with the eyelid skin could burn it. Therefore, clinicians and patients must proceed with caution [15]. The upper outer eyelids may reach the peak temperature (40.1 °C) after 2 min of treatment. Then, the heat may remain stable and decrease to 37.9 °C after 12 min [16] Tichenor et al. [28] (I) compared the application of the BRUDER Compress once versus twice a day. Although an improvement in MG scores and symptoms was observed for both treatment regimens, DED symptoms decreased more when applying the compress once a day. Nonetheless, these results were attributed to the higher compliance observed in the once-a-day group.

The Eye-ssential® Mask (Thera Pearl, USA) produces warmth when the pearls inside the mask absorb, hold and deliver the heat acquired in the microwave. The mask reaches its peak temperature (38.7 °C) after 3 min and decreases to 37.9 °C after 12 min [16].

The Blephasteam® (Théa Laboratories, France) is a goggle system that produces moist warm air and heats the eyelids through the condensation of water vapor. The melted meibum secretion is favoured by the normal blinking of the patients during the treatment. Temperatures recorded in the outer upper eyelids were between 37.4 °C and 40.0 °C at the end of the treatment, while in the lower ones they were between 37.8 °C and 38.4 °C [27, 29].

Two studies (III) suggested that Blephasteam® might be a safe and effective therapy for MGD because DED symptoms and MG function improved after 21 days of treatment [30, 31]. Ocular symptoms and clinical signs, except the conjunctival redness score, may achieve a higher improvement after Blephasteam® than after warm compresses (III) [32]. However, in another study (I), signs improved equally in both therapies [33]. Nonetheless, Blephasteam® may be useful for subjects who find warm compresses ineffective (III) [34].

Warming and Massaging Devices

These devices apply heat to the eyelids to liquefy the meibum and then apply a mechanical pressure to deliver the meibum to the ocular surface.

The LipiFlow® system (Johnson & Johnson Vision, USA) applies heat (42.5 °C) and simultaneous pulsated pressure to the inner upper and lower eyelids for 12 min. The device consists of an eyelid warmer that applies the heat and an eye cup that applies the pressure through an inflatable air bladder [35].

Regarding its effectiveness, a retrospective case series study (III) showed that symptoms, MG function, lipid layer thickness (LLT), partial blink rate, and tear break-up time (BUT) improved 4 and 12 weeks after the treatment [36].

Some studies compared LipiFlow® with other MGD management strategies. Almost all of the studies comparing the LipiFlow® with traditional eyelid hygiene (I and III) found an improvement in symptoms in the LipiFlow® group [37,38,39,40]. Only two studies (III) found an improvement in signs, such as MG secretion and BUT [39, 41]. Other authors compared LipiFlow® with other medical devices, such as Tauber et al. [42] (I), who compared LipiFlow® with iLux® and did not find differences between the two treatments. Another study (II) reported that one single LipiFlow® session was more effective in decreasing DED symptoms compared to 3 months of oral doxycycline [43]. Finally, Yeo et al. [44] (I) showed a significant reduction in the tear evaporation rate after 4 and 12 weeks of LipiFlow® treatment, in contrast to EyeGiene® and Blephasteam®.

It was also reported that the LipiFlow® system produced successful results in patients with other conditions such as Sjögren syndrome (III) [45], dry eye after laser correction surgery (III) [41], and symptomatic contact lens wearers (I) [46].

Concerning the treatment duration, Greiner et al. [47, 48] conducted a study (III) with different follow-up periods. While the MG score, BUT, and symptoms improved at 9 and 12 months compared to baseline, the improvement was only sustained in the MG score and symptoms after 3 years [49]. The improvement in MG score and symptoms after 12 months agreed with the results of Blackie et al. [50] (I). In addition, Finis et al. [51] (III) also reported an improvement in ocular signs 6 months after treatment, such as LLT, the number of lid-parallel conjunctival folds, and bulbar conjunctival redness.

Several authors have tried to predict the success of the LipiFlow® treatment based on different parameters. Satjawatcharaphong et al. [52] (III) suggested that it depended on gender, DED symptoms, and non-invasive tear break-up time (NIBUT). However, another study (III) proposed that patients with lower tear production and higher ocular surface staining and osmolarity could also respond positively to the LipiFlow® treatment [53]. The discrepancies between both studies could result from the different follow-up times. In the first study, it ranged between 21 and 84 days, while in the second one, it ranged between 30 and 40 days.

Massaging Eyelid Devices

These devices facilitate the mechanical release of meibum, which has to be performed manually in conventional eyelid hygiene.

The Eyepeace eyelid massage device (Eyepeace, UK) is a self-administered silicone device for massaging the eyelids to improve meibum expression. A study (I) compared the efficacy of this device with manual eyelid massage [54]. After 2 weeks of treatment, the increase in LLT was greater in the eyes treated with the Eyepeace.

Cleaning Devices

These devices remove the bacterial biofilm, debris, and scurf present in the MG ducts, which could occlude them and therefore prevent meibum delivery.

The MG probing consists of the insertion of probes of different sizes in the MG ducts to dilate them and permit the subsequent meibum expression. It requires the eye to be anesthetized [55]. MG probing has been found to decrease DED symptoms 1 and 6 months after the treatment (III) [56]. Sik Sarman et al. [57] (III) treated patients using a modified cannula to reduce pain and bleeding. After the procedure, patients were prescribed antibiotics, corticosteroids, artificial tears, and eyelid massage. Most of the patients had severe MGD and required more than one session. After 3 months, BUT, conjunctival hyperaemia, eyelid margin vascularity, and DED symptoms decreased.

The NuLids (NuSight Medical, USA) is a home-use device that has a disposable silicone tip that massages the eyelids to remove biofilm and scurf [58].

The BlephEx (Blephex LLC, USA) is a hand-held device for removing bacterial biofilm and debris from the eyelid [59, 60]. Murphy et al. [59] (III) studied the effectiveness of one session of BlephEx and the subsequent nightly application of OcuSoft Lid Scrub Plus foam on patients with Demodex folliculorum blepharitis. They showed that the symptomatology and the quantity of Demodex folliculorum decreased 2 and 4 weeks after the treatment. Epstein et al. [60] (I) evaluated the effectiveness of the Blephex at the beginning of the study and after 1 month in patients with Demodex blepharitis. In addition, some of the patients used terpinen-4-ol eyelid scrubs twice daily for 2 months, while others used sham scrubs. The Demodex level decreased after 2 months in patients who used terpinen-4-ol, while it decreased after 1 and 2 months in patients who used sham scrubs. However, no changes in ocular symptoms were found. Regarding the ocular signs, patients who used sham scrubs worsened tear production and improved blepharitis signs and the ease of MG expression after 1 and 2 months.

Light-Based Devices

These devices apply light directly on the skin near the eyelids to treat MGD.

The intense pulsed light (IPL) devices are high-intensity, non-coherent, and non-laser light sources ranging from 500 to 1200 nm [61]. Patients are fitted with safety goggles covering both eyes during the treatment. The skin treatment area requires an ultrasound gel. Light pulses are applied into the cheek skin, near the lower eyelids. However, one study (I) evaluated the technique applying pulses directly into the upper eyelids [62]. A higher improvement in MG secretion function was found in the lower eyelids than in the upper eyelids. This was attributed to the smaller tear meniscus present in the upper eyelids, which contains fewer inflammatory proteins.

The number of light pulses required to improve MGD has been addressed in the clinical trial of Xue et al. [63] (I). They reported that applying five light pulses instead of four seemed to achieve higher and earlier improvements in clinical signs and DED symptoms.

One of the proposed mechanisms of IPL to improve MGD is the reduction of the bacterial load of the eyelid margin that could alter meibum secretion or obstruct MG ducts [64, 65]. Xue et al. [63] (I) observed an inhibition of Corynebacterium macginleyi growth after IPL treatment, although the effect was not observed in all the bacterial species evaluated. Conversely, Albietz et al. [66] (III) found no short-term changes in the eyelid margin colony counts cultured after IPL treatment. Another proposed mechanism is that IPL may increase the skin temperature and the heat could be absorbed by haemoglobin to eliminate the superficial blood vessels, especially when they are large [67]. The MG inflammation would be reduced by the removal of these blood vessels [68] and also because of photomodulation. According to the studies by Liu et al. [69] and Piyacomn et al. [70] (I), this process would reduce some inflammatory mediators such as interleukin (IL)-17A, IL-6, or IL-1Ra.

Two commercial IPL devices are widely used for MGD treatment: the E > Eye system (E-SWIN, France), also called Intense Regulated Pulsed Light (IRPL), and the M22 system (Lumenis, Israel), also called Optimal Pulse Technology (OPT™). There are some differences between both devices such as the treatment schedule. The E > Eye system is usually applied in three or four sessions, performed on days 1, 15, 45, and 75 [63, 70, 71], while the M22 system is usually applied in three sessions, separated by 3 or 4 weeks [62, 71, 72]. The spot size is 15 × 40 mm in E > Eye and 15 × 35 mm in the M22, and the cooling system is Airflow in the E > Eye and ChillTip™ Contact in the M22. These differences might be the reason why Wu et al. [71] (I) found discrepant results when comparing both devices. They found that the MG secretion function and tear film quality improved more after the M22 than after the E > Eye treatment.

Regarding the efficacy, some studies assessed IPL treatment alone. Jiang et al. [73] (III) observed an improvement in symptoms, BUT, conjunctival injection, and MG score from baseline to day 45. However, no differences were found between days 75 and 45, suggesting that two sessions were enough to reduce the signs and symptoms of MGD. Vigo et al. [74] (III) also performed follow-up visits on day 1, 15, and 45. They found an improvement in NIBUT, LLT, and osmolarity and suggested that patients with lower BUT responded better to the treatment. Finally, Yurtasser et al. [75] (III) found an improvement in symptoms and NIBUT at 1 month and an improvement in symptoms, NIBUT, MG dropout, and corneal staining in the mild and moderate MG atrophy groups, lasting up to 12 months. No improvement was observed in patients with severe MG atrophy. However, another study (II) compared IPL with eyelid hygiene and found that although both groups improved in symptoms, BUT, and MG score; the IPL group also improved in conjunctival staining [76].

Several studies evaluated the IPL treatment along with other treatments. Piyacomn et al. [70] (I) observed a higher and faster improvement in the MG function in patients who combined conventional eyelid hygiene and IPL than in those patients who performed hygiene alone. Huang et al. [72] (I) compared IPL with intraductal MG probing. They reported that the combination of both methods was more effective than separately in improving symptoms, BUT, meibum grade, and telangiectasias. IPL alone was more suitable for relieving intraductal inflammation, while MG probing was better for patients with severe MG obstruction or MG scarring. Some studies combined IPL treatment with MG expression. While Toyos et al. [77] (II) only found an improvement in symptoms and BUT, Dell et al. [78] (III) also observed improvements in MG score and corneal staining. However, Arita et al. [79] conducted a randomized clinical trial (I) comparing a combined therapy and MG expression alone. They found an improvement in the symptoms, NIBUT, BUT, and MG score in both therapies. However, the improvement was higher after the combined therapy, and this group also improved the LLT and corneal staining.

There is a lack of agreement in the IPL treatment protocol. The number of sessions varies among three [74, 76], four [73, 77, 78], and eight [79], and the period between sessions can fluctuate between 15 [73, 74, 77], 21 [78, 79] and 30 [76, 77] days. Finally, the number of flashes is not standardized, 4–5 being the most frequent [73,74,75, 80], although other authors double the flashes or apply even more [78, 79].

Massaging and Light-Based Devices

These devices combine the application of pressure to the eyelids along with the light-based therapeutic effect to facilitate the release of meibum to the ocular surface.

The iLux® (Alcon, USA) is a handheld device that applies light-based heat and compression to the eyelids. An inner pad slips behind the eyelid and an outer pad is pressed against the outer surface of the eyelid [58]. As mentioned above, a clinical trial (I) compared the effectiveness of LipiFlow® and iLux®, without finding differences [42].

Conclusion

New therapies for MGD management are continuously becoming commercially available, which help clinicians and patients to better cope with the anomaly. There are several warming and humidity devices as well as eyelid massaging and cleaning devices that have showed improvement of MGD. However, treatment sessions must be performed regularly to maintain the therapeutic effect. Other instruments based on thermal pulsation and intense pulsed light technology have also demonstrated their ability to improve the MGD status for a longer time, and even in only one session, in case of thermal pulsation. The wide variety of commercial devices can allow clinicians to adequately counsel patients based on the MGD severity and therapeutic compliance.