PMID- 38068417 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231209 IS - 2077-0383 (Print) IS - 2077-0383 (Electronic) IS - 2077-0383 (Linking) VI - 12 IP - 23 DP - 2023 Nov 28 TI - Assessing the Effects of 0.3% Carboxymethylcellulose Tear Substitute Treatment on Symptoms and Signs of Dry Eye Disease in Elderly Population: A Prospective Longitudinal Study. LID - 10.3390/jcm12237364 [doi] LID - 7364 AB - BACKGROUND: We aimed to evaluate the effects of 0.3% carboxymethylcellulose (CMC) tear substitute treatment in dry eye disease (DED), as well as treatment compliance and adverse events (AEs). METHODS: In this prospective, longitudinal study, a total of 30 eyes receiving 0.3% CMC tear substitute four times daily for DED were evaluated. Clinical endpoints included an ocular surface disease index (OSDI) questionnaire, average non-invasive tear film break-up time (A-NIBUT), lipid layer thickness (LLT), and a Schirmer test with anesthesia (ST). Treatment compliance and AEs were also assessed. All evaluations were performed at 2, 4, and 12 weeks of follow-up. RESULTS: At the end of the follow-up, significant improvement was observed in all clinical endpoints with the following mean values: DeltaOSDI questionnaire of -22.53 +/- 14.68 points, DeltaA-NIBUT of 4.81 +/- 2.88 s, DeltaLLT of 5.63 +/- 6.53 nm, and DeltaST of 2.8 +/- 2.1 mm (p < 0.001 for all comparisons). Although repeated measures analysis showed that all clinical endpoints presented statistically significant differences (p < 0.001 for all comparisons LLT(Baseline)-LLT(2-weeks) (p = 0.460) and LLT(4-weeks)-LLT(12-weeks) (p = 0.071) were the only pairs of measures that reported non-statistically significant differences). In addition, treatment compliance was 94.3 +/- 5.2% and transient AEs related to the use of 0.3% CMC tear substitute were reported. CONCLUSIONS: 0.3% CMC tear substitute treatment seems to achieve beneficial effects on the OSDI questionnaire, A-NIBUT, LLT, and ST. However, further studies at this concentration are needed to confirm these results. FAU - Ballesteros-Sanchez, Antonio AU - Ballesteros-Sanchez A AUID- ORCID: 0000-0002-9248-8685 AD - Department of Physics of Condensed Matter, Optics Area, University of Seville, 41004 Seville, Spain. AD - Department of Ophthalmology, Clinica Novovision, 30008 Murcia, Spain. FAU - Sanchez-Gonzalez, Jose-Maria AU - Sanchez-Gonzalez JM AUID- ORCID: 0000-0003-0450-7717 AD - Department of Physics of Condensed Matter, Optics Area, University of Seville, 41004 Seville, Spain. FAU - Tedesco, Giovanni Roberto AU - Tedesco GR AUID- ORCID: 0000-0003-1350-3398 AD - Studio Oculistica Tedesco, 88024 Girifaldo, Italy. FAU - Rocha-De-Lossada, Carlos AU - Rocha-De-Lossada C AUID- ORCID: 0000-0001-7464-2493 AD - Qvision, Ophthalmology Department, VITHAS Almeria Hospital, 04120 Almeria, Spain. AD - Ophthalmology Department, VITHAS Malaga, 29016 Malaga, Spain. AD - Regional University Hospital of Malaga, Hospital Civil Square, 29009 Malaga, Spain. AD - Department of Surgery, Ophthalmology Area, University of Seville, 41009 Seville, Spain. FAU - Murano, Gianluca AU - Murano G AD - Sacro Cuore-iGreco Ospedali Riuniti, 87100 Cosenza, Italy. FAU - Spinelli, Antonio AU - Spinelli A AD - Biomeeting, 89123 Reggio Calabria, Italy. FAU - Borroni, Davide AU - Borroni D AUID- ORCID: 0000-0001-6952-5647 AD - Departament of Ophthalmology, Riga Stradins University, LV-1007 Riga, Latvia. AD - Centro Oculistico Borroni, 21013 Gallarate, Italy. AD - Eyemetagenomics Ltd., London WC2H 9JQ, UK. LA - eng PT - Journal Article DEP - 20231128 PL - Switzerland TA - J Clin Med JT - Journal of clinical medicine JID - 101606588 PMC - PMC10707251 OTO - NOTNLM OT - artificial tears OT - carboxymethylcellulose (CMC) OT - dry eye disease (DED) OT - meibomian gland dysfunction (MGD) OT - tear substitutes COIS- Author Davide Borroni was employed by the company Eyemetagenomics. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/12/09 10:43 MHDA- 2023/12/09 10:44 PMCR- 2023/11/28 CRDT- 2023/12/09 01:10 PHST- 2023/10/11 00:00 [received] PHST- 2023/11/13 00:00 [revised] PHST- 2023/11/27 00:00 [accepted] PHST- 2023/12/09 10:44 [medline] PHST- 2023/12/09 10:43 [pubmed] PHST- 2023/12/09 01:10 [entrez] PHST- 2023/11/28 00:00 [pmc-release] AID - jcm12237364 [pii] AID - jcm-12-07364 [pii] AID - 10.3390/jcm12237364 [doi] PST - epublish SO - J Clin Med. 2023 Nov 28;12(23):7364. doi: 10.3390/jcm12237364.