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74 protocols using cravit

1

Postoperative Management for Standardized DMEK

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In the staged group, patients were administered 1.5% levofloxacin (Cravit; Santen, Osaka, Japan) and betamethasone (Sanbetason; Santen) 4 times daily and bromfenac (Bronuck; Senju Pharmaceutical Co, Osaka, Japan) 2 times daily between cataract surgery and the DMEK procedure.
Standardized DMEK was performed as previously reported.10 (link),11 (link) After surgery, 0.4 mg of betamethasone (Rinderon; Shionogi, Osaka, Japan) was injected subconjunctivally and 1.5% levofloxacin eye drops (Cravit; Santen) were instilled. Two hours after completing surgery, slit-lamp examination was conducted and intraocular pressure was checked. All patients were instructed to remain supine for several days until the air in the anterior chamber (AC) had disappeared. Postoperative medications included 1.5% levofloxacin (Cravit; Santen) and betamethasone (Sanbetason; Santen) 4 times daily for 3 months and tapered thereafter. Topical tropicamide was not included in the postoperative regimen.
When CME was diagnosed postoperatively, topical bromfenac (Bronuck; Senju Pharmaceutical Co) and a sub-Tenon injection of triamcinolone acetonide (MaQaid; Wakamoto Pharmaceutical Co, Tokyo, Japan) were immediately applied and administered, respectively. After cataract surgery, postoperative medications included topical bromfenac as well as 1.5% levofloxacin and betamethasone.
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2

Postoperative Care in Corneal Refractive Procedures

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The postoperative care was similar for the four procedures. One drop of tobramycin/dexamethasone (Tobradex; Alcon, TX, United States) was instilled at the surgical site. A bandage contact lens (Acuvue Oasys; Johnson & Johnson, FL, United States) was then placed on the cornea and kept for 1 day in the FS-LASIK and FS-LASIK Xtra groups until complete re-epithelization in the tPRK and tPRK Xtra groups–typically between 5 and 7 days. Topical levofloxacin 0.5% (Cravit; Santen, Osaka, Japan) was used until the bandage lens was taken off. This was followed by application of fluorometholone 0.1% (Flumetholon; Santen, Osaka, Japan), topical levofloxacin 0.5% (Cravit; Santen, Osaka, Japan), and dexamethasone (Tobradex; Alcon, Rijksweg, Belgium) whose frequency, duration, and tapering regime varied between the procedures as shown in Figure 2.
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3

Postoperative Eye Drop Regimen for EVO-ICL vs SMILE

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The following eye drops were used in the EVO-ICL group: 0.5% levofloxacin (Cravit; Santen, Osaka, Japan) four times daily for 7 days; 1.0% prednisolone acetate (Pred Forte; Allergan, Irvine, CA, United States) four times a day for 4 days; Pranoprofen (Senju, Osaka, Japan) was used four times a day for 14 days; and artificial tears (Hyalein, 0.1% hyaluronic acid, Santen) four times daily for 1 month.
The following eye drops were used in the SMILE group: 0.5% levofloxacin (Cravit; Santen, Osaka, Japan) four times daily for 7 days; 0.1% Fluorometholone (Fluorometholone; Santen, Osaka, Japan) eight times daily and tapered to one time daily for over 24 days; and artificial tears (Hyalein, 0.1% hyaluronic acid, Santen) four times daily for 3 months.
The length of follow-up was 2 years.
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4

Corneal Endothelial Cryodamage in Rabbits

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A combination of tiletimine and zolazepam-mixed agent (ZoletilTM, Virbac, Fort Worth, TX, USA) and xylazine (RompunTM, Bayer, Leverkusen, Germany) was injected intramuscularly for anesthesia (12.5 mg/kg). The corneal endothelium of rabbits was cryo-damaged according to the established protocol by Okumura et al.62 (link). In brief, a stainless steel probe with a diameter of 7 mm was immersed in liquid nitrogen tank for 3 minutes to achieve a stabilized temperature of approximately −196 °C. Thereafter, corneal endothelium was damaged by transcorneal freezing by gently touching the central corneal surface with the probe for 15 seconds as noted in Fig. 3C. The ocular surface was then irrigated using 10 mL of normal saline. Topical levofloxacin eye drops (CravitTM, Santen, Osaka, Japan) were applied 4 times a day for 3 days to prevent infection.
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5

Wavefront-guided LASIK with Technolas 217z

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Wavefront-guided LASIK was performed with the Technolas 217z excimer laser system (Bausch & Lomb) to apply a flying spot of 1.0 or 2.0 mm in diameter with a Gaussian profile and a 120 Hz active eye tracker. The LSK-1 microkeratome (Moria, Antony, France) was utilized for creating a hinged corneal flap of 130-μm thickness. Postoperatively, steroidal (0.1% fluorometholone, Flumetholone TM, Santen) and antibiotic (0.3% levofloxacin, CravitTM, Santen) medications were topically administered 4 times daily for 2 weeks.
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6

Posterior Chamber ICL Implantation Procedure

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The patients preoperatively underwent 2 peripheral iridotomies with a neodymium-YAG laser. On the day of surgery, the patients were given dilating and cycloplegic agents. After topical anesthesia, a model V4b ICL (without a central hole) was inserted through a 3-mm clear corneal incision with the use of an injector cartridge (STAAR Surgical) after placement of a viscosurgical device (OpeganTM; Santen, Osaka, Japan) into the anterior chamber. The ICL was placed in the posterior chamber, the remaining viscosurgical device was completely washed out from the anterior chamber with balanced salt solution, and a miotic agent was instilled. For toric ICL implantation, to control for potential cyclotorsion in a supine position, the zero horizontal axis was marked preoperatively using a slit-lamp. After the ICL had then been placed in the posterior chamber and rotated by 22.5 degrees or less using the manipulator. Postoperatively, steroidal (0.1% betamethasone, RinderonTM, Shionogi, Osaka, Japan) and antibiotic (0.3% levofloxacin, CravitTM, Santen, Osaka, Japan) medications were administered topically 4 times daily for 2 weeks, and the dose was steadily reduced thereafter.
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7

Pterygium Excision and Cataract Surgery Protocol

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For primary pterygium surgery, after subconjunctival injection of lidocaine-epinephrine (1:100,000) into the tissue, the pterygium head was bluntly lifted off from the cornea, and the pterygium head and body were excised at ∼4 mm from the limbus. Abnormal subconjunctival fibrous tissue was trimmed away, and abnormal scarring on the cornea was polished. A conjunctival autograft was moved from the superior bulbar conjunctiva in order to cover the defect area with 8–0 absorbable polyglycolic sutures without the use of mitomycyin C.
For cataract surgery, standard phacoemulsification was performed. The surgical technique consisted of a capsulorhexis, nucleus and cortex extraction, and a monofocal IOL (AQ-110NV, Staar Surgical, CA) implantation through a temporal 2.8-mm clear corneal incision. All surgeries were uneventfully performed by 1 experienced surgeon (K.K.) using the same technique. In 43 of 60 eyes, we selected emmetropia as the target refraction. In the remaining 17 eyes, we intentionally selected a slight myopia for near vision. Postoperatively, steroidal (0.1% betamethasone, RinderonTM, Shionogi, Osaka, Japan), antibiotic (0.3% levofloxacin, CravitTM, Santen, Osaka, Japan), diclofenac sodium (0.1% DiclodTM, Wakamoto, Tokyo, Japan) medications were topically administered 4 times daily for 1 month, the dose being reduced gradually thereafter.
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8

Standardized ICL Implantation Technique

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All ICL implantation surgeries were performed using a standardized method in all surgical centers. After topical anesthesia, ICL was inserted through a 3-mm clear corneal incision using an injector cartridge (STAAR Surgical) after placement of a viscosurgical device (Opegan; Santen, Osaka, Japan) into the anterior chamber. The ICL was placed in the posterior chamber, the viscosurgical device was completely washed out of the anterior chamber with a balanced salt solution, and a myotic agent was instilled. All surgeries were uneventful, and no intraoperative complication was observed. After surgery, steroids (0.1% betamethasone; Rinderon; Shionogi, Osaka, Japan) and antibiotics (0.3% levofloxacin; Cravit; Santen, Osaka, Japan) were topically administered four times daily for two weeks, and the dose was gradually reduced thereafter.
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9

ICL Implantation Procedure Protocols

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ICL V4c implantation procedures were performed by the same experienced surgeon. Preoperatively, levofloxacin (Cravit; Santen, Osaka, Japan) eye drops were applied topically four times daily for 3 days. The pupils were fully dilated (Tropicamide Phenylephrine Eye Drops) and surface anesthesia (Proparacaine Hydrochloride Eye Drops) was performed before surgery. A 3.0 mm corneal incision was made at the temporal side of the eye, and the ICL was inserted into the anterior chamber. After the ICL had unfolded naturally, a viscoelastic agent was injected to maintain the appropriate anterior chamber depth. The ICL loop was placed into the posterior ciliary sulcus of the iris (with a positioning hook) and in the center of the ICL optical area. Subsequently, the viscoelastic surgical agent was completely removed using a balanced salt solution. Eye ointment was applied to the conjunctival sac and the eye was covered after the operation. After surgery, the patients were given levofloxacin eye drops four times daily for 1 week.
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10

Infectious Keratitis Treatment Protocol

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The patients diagnosed with infectious keratitis were treated following the protocol used in previous studies [13 (link)-15 (link)]. All patients with fungal keratitis were treated hourly with 5% natamycin, alone or combined with 0.25% amphotericin B. All patients also received 400 mg of itraconazole orally per day. Patients suspected of having a bacterial ulcer received topical antibiotic treatment with 0.5% Cravit (Santen Pharmaceutical (China) Co, Ltd, Suzhou, China) every hour while awake for the first 48 h, while the culture results were pending.
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