Abstract

•Serial conjunctiva sampling for RT-PCR for SARS-CoV2 in a group of 39 COVID19 patients showed low detection rate•High level of personal hygiene including face mask, adequate eye protection and mobile phone disinfection is crucial in preventing SARS-CoV2 from affecting the eyes, be it conjunctiva or cornea, both at beginning as well as throughout the COVID19 disease course. To date, there remain many unknowns regarding ocular involvement in COVID-19. Various studies have reported conflicting rates of conjunctival carriage of SARS-CoV-2 (Table 1). A cross-sectional study on 1099 patients in China found only 0.8% of COVID-19 patients developed conjunctival congestion,1Guan WG Ni ZY Hu Y Liang WH Ou CQ He JX et al.Clinical characteristics of coronavirus disease 2019 in China.N Engl J Med. 2020; 382: 1708-1720Crossref PubMed Scopus (17227) Google Scholar whereas a recent meta-analysis found the pooled prevalence of ocular manifestations among COVID-19 patients was 5.5% and the sensitivity of detecting SARS-CoV-2 in ocular fluids was merely 0.6%.2Ulhaq ZS Soraya GV. The prevalence of ophthalmic manifestations in COVID-19 and the diagnostic value of ocular tissue/fluid.Graefes Arch Clin Exp Ophthalmol. 2020; : 1-2Google Scholar The low detection rate may suggest a low incidence of viral infiltration into ocular surface or may be due to variations in sampling technique, sampling time window, and underrepresentation from critical cases. To provide an answer, we set out to standardize the sampling technique and sampling time to minimize the chance of false negative results and to gauge whether SARS-CoV-2 can really infect the ocular surface.Table 1Summary of existing studies on the presence of SARS-CoV-2 in ocular secretionsReferenceSample SizeNo. of patients with ocular symptomsMethodologyPositive findings (RT-PCR for SARS-CoV-2)ConclusionXia et al.10Xia J Tong J Liu M Shen Y Guo D. Evaluation of coronavirus in tears and conjunctival secretions of patients with SARS-CoV2 infection.J Med Virol. 2020; : 1-6PubMed Google Scholar30 patients(21 mild disease9 severe disease)1 (conjunctivitis)Conjunctival swab2 samples from 1 patient with conjunctivitisSARS‐CoV‐2 may be detected in the tears and conjunctival secretions in NCP patients with conjunctivitisWu et al.11Wu P Duan F Luo C Liu Q Qu X Liang L et al.Characteristics of ocular findings of patients with coronavirus disease 2019 (COVID-19) in Hubei Province, China.JAMA Ophthalmol. 2020; 138: 575-578Crossref PubMed Scopus (760) Google Scholar38 patients12 (conjunctivitis, chemosis)Conjunctival swab2One-third of patients in the sample group had ocular symptoms; it is possible for the virus to be transmitted through the eyesZhou et al.12Zhou Y Duan C Zeng Y Tong Y Nie Y Yang Y et al.Ocular findings and proportion with conjunctival SARS-COV-2 in COVID-19 patients.Ophthalmology. 2020; 127: 982-983Abstract Full Text Full Text PDF PubMed Scopus (130) Google Scholar121(63 mild–moderate disease58 severe disease)8 (3 patients with redness, others included itchiness, tearing)Conjunctival swab1 patient with ocular symptoms, 2 patients without ocular symptomsThe proportion with positive results for SARS-CoV-2 RNA was significantly less in the conjunctival and nasopharyngeal specimensSeah et al.13Seah IYJ Anderson DE Kang AEZ Wang L Rao P Young BE et al.Assessing viral shedding and infectivity of tears in coronavirus disease 2019 (COVID-19) patients.Ophthalmology. 2020; 127: 977-979Abstract Full Text Full Text PDF PubMed Scopus (294) Google Scholar17 patients (64 samples were obtained over the study period)1 (conjunctivitis after admission)Schirmer's strip (tears)0Transmission through tears regardless of the phase of infection likely is lowZhou et al.14Zhou Y Zeng Y Tong Y Chen C. Ophthalmologic evidence against the interpersonal transmission of 2019 novel coronavirus through conjunctiva [Preprint article].MedRxiv. 2020; (02.11.20021956)Google Scholar63 confirmed cases1 (conjunctivitis)Conjunctival swab1 definite positive, 2 probable positive PCR result(none had ocular symptoms)2019−nCoV can be detected in the conjunctival sac of patients with NCP (novel virus pneumonia)Hui et al.15Hui KP Cheung MC Perera RAPM Ng KC Bui CHT Ho JCW et al.Tropism, replication competence, and innate immune responses of the coronavirus SARS-CoV-2 in human respiratory tract and conjunctiva: an analysis in ex-vivo and in-vitro cultures.Lancet Respir Med. 2020; 8: 687-695Abstract Full Text Full Text PDF PubMed Scopus (328) Google Scholar1Ex vivo studyResearchers isolated SARS-CoV-2 from a patient with confirmed COVID-19 and assessed infection using ex vivo cultures of human conjunctivaSARS-CoV-2 infected the conjunctival mucosaConjunctival epithelium appear to be potential portals of infection for SARS-CoV-2Li et al.16Li X Chan JFW Li KKW Tso EYK Yip CCY Sridhar S et al.Detection of SARS-CoV-2 in conjunctival secretions from patients without ocular symptoms [Online ahead of print.Infection. 2020; (September 17)Crossref Scopus (28) Google Scholar490Conjunctival swab4 patientsSARS-CoV-2 can be present on the conjunctiva in the absence of ocular symptomsRT-PCR, reverse transcription–polymerase chain reaction; NCP, novel coronavirus pneumonia; nCoV, novel coronavirus. Open table in a new tab RT-PCR, reverse transcription–polymerase chain reaction; NCP, novel coronavirus pneumonia; nCoV, novel coronavirus. We conducted a prospective study by adopting standardized technique for conjunctiva sampling via clear protocol and instructional video (see supplementary video). Adequate tissue sampling was ensured by sweeping lower tarsal conjunctiva twice. In cases of unilateral eye redness, only the involved eye was sampled to avoid transmitting any microorganisms to the uninvolved eye. Two serial eye swabs were taken, one on admission (presentation sample) and another before hospital discharge (convalescent sample), to gauge whether viral shedding was present on the conjunctiva at the beginning and end of the COVID-19 disease course. A total of 78 eye swab samples were obtained from 39 consecutive COVID-19 patients admitted to a regional hospital in Hong Kong. Patient's medical history, ocular symptoms, nasopharyngeal SARS-CoV-2 results, and personal hygiene habits were prospectively collected and analyzed. The eye swab specimens underwent real-time reverse transcription–polymerase chain reaction (rRT-PCR) testing using the E gene assay, where a 76-bp-long fragment from a conserved region in the E gene would be detected by labeled hydrolysis probes using real-time PCR. The reagent used was TIB MOLBIOL LightMix®-Roche Diagnostics, Modular SARS and Wuhan CoV E-gene, Cat.-No. 53-0776-96. The results of specimen for rRT-PCR of SARS-CoV-2 was reported with corresponding cycle thresholds for positive specimen. All 39 cases had proven COVID-19 disease by respiratory samples for SARS-CoV-2 RT-PCR (Table 2). The mean age was 40 (range 19–72), with equal gender representation. Of note, most patients in our case series had mild to moderate COVID-19 disease (89.74%); 15.38% (6/39) reported symptoms suggestive of ocular surface inflammation, including epiphora (10.25%), itchiness (7.69%), and foreign body sensation (5.13%). However, only 1 patient (2.56%) had bilateral overt conjunctivitis, which began 2 days after onset of mild Upper Respiratory Tract Infection (URTI) symptoms and spontaneously resolved after 1 week. There was no correlation between the COVID-19 severity and ocular symptoms (p = 0.308).Table 2Demographic characteristics, ocular protection, and personal hygiene habits of 39 COVID-19 patients in our case seriesNo. of patients (percentage of total)Female19 (48.71%)Male20 (51.28%)Age40 y (range: 19–72)Medical comorbidityHT4 (10.26%)Multiple sclerosis1 (2.63%)Hx of thyrotoxicosis2 (5.13%)DM1 (2.63%)COVID disease severityMild29 (74.36%)Moderate6 (15.38%)Severe3 (7.69%)Critical1 (2.56%)Ocular symptomsEpiphora4 (10.26%)Itchiness3 (7.69%)Foreign body sensation2 (5.13%)Redness1 (2.56%)Discharge1 (2.56%)Eye protection and personal hygiene habits (protective factors)Spectacles (total)30 (76.92%)Full-time glasses16 (41.03%)Reading glasses/PRN14 (35.90%)Googles3 (7.69%)Hand washing frequencyHourly18 (46.15%)4–5 times/day21 (53.85%)Mobile phone cleaning with alcohol pad/spray30 (76.92%)Risk factorsFrequent eye rubbing9 (23.07%)Regular eyedrop use8 (20.51%)Contact lens11 (28.21%)Touching of eyes after touching face mask11 (28.21%)HT, hypertension; DM, diabetes mellitus; Hx, history; PRN, as needed. Open table in a new tab HT, hypertension; DM, diabetes mellitus; Hx, history; PRN, as needed. All cases had conjunctival sampling for SARS-CoV-2 on day 1 postadmission and before hospital discharge (days 4–40). On average, the first swab was taken on day 6 since the onset of COVID-19 symptoms. The corresponding cycle threshold in matching nasopharyngeal samples was 29.81 on admission, which is indicative of intermediate to low viral load.3Bruce EA Huang ML Perchetti GA et al.Direct RT-qPCR detection of SARS-CoV2 RNA from patient nasopharyngeal swabs without an RNA extraction step [Preprint article].bioRxiv. 2020; Google Scholar In all 78 conjunctival samples, SARS-CoV-2 was not detected by RT-PCR. This was true across the spectrum of COVID-19 disease severity. There are 2 possible explanations for viral nondetection in the conjunctiva in our study. Hypothetically, the various means of personal hygiene (Table 2) reported in our patients could partially account for the low transmission rate onto the conjunctiva surface both before and during the COVID-19 disease course (e.g., via self-inoculation). Because of the high level of vigilance in Hong Kong, the local residents have adopted stringent personal hygiene since early reports of COVID-19 in January 2020. This was reflected in our study participants, who had adopted universal face masking (100%), 4 times or more handwashings per day (100%), and daily mobile phone disinfection with alcohol wipes (76.92%). Other ocular protection included that 76.92% wore spectacles while 7.69% more wore goggles. Regarding risk factors of ocular transmission, 28.95% of study participants wore contact lenses, including the patient with conjunctivitis, who had worn daily disposable contact lenses. On the other hand, the presence of active conjunctivitis symptoms without the detection of SARS-CoV-2 RNA on the conjunctiva may suggest ocular symptoms are a part of a systemic immunologic response instead of resulting from direct inoculation. There have been several reports on immunologic phenomenon associated with SARS-CoV-2, such as paediatric multisystem inflammatory syndrome,4Royal College of Paediatrics and Child Health. Guidance: Paediatric multisystem inflammatory syndrome temporally associated with COVID-19. https://www.rcpch.ac.uk/sites/default/files/2020-05/COVID-19-Paediatric-multisystem-%20inflammatory%20syndrome-20200501.pdf 2021Google Scholar Guillain-Barré syndrome,5Gupta A Paliwal VK Garg RK. Is COVID-19-related Guillain-Barré syndrome different?.Brain Behav Immun. 2020; 87: 177-178Crossref PubMed Scopus (18) Google Scholar and the observation of cytokine storm, where the imbalance between inflammatory innate response and impaired adaptive host immune defense led to systemic tissue damage and manifestations. However, if this hypothesis holds true, one would speculate that ocular involvements are likely to occur in COVID-19 patients with more severe disease systemically. We believe that the simpler hypothesis of the ocular surface being infected by the virus (either via droplet transmission or via self-inoculation) is more likely. The risk of self-inoculation exists. As reported by a cross-sectional study of 534 patients, COVID-19 seldom presents initially with conjunctivitis (0.56%). In contrast, 4.12% developed conjunctivitis after systemic symptoms.6Chen L Deng C Chen X Zhang X Chen B Yu H et al.Ocular manifestations and clinical characteristics of 534 cases of COVID-19 in China: a cross-sectional study [Preprint article].MedRxiv. 2020; (03.12.20034678)Google Scholar A COVID-19 case was also reported to develop follicular conjunctivitis with positive conjunctival carriage not at the beginning but late in the disease (day 13), amid antiviral treatments.7Chen L Liu M Zhang Z Qiao K Huang T Chen M et al.Ocular manifestations of a hospitalised patient with confirmed 2019 novel coronavirus disease.Br J Ophthalmol. 2020; 104: 748-751Crossref PubMed Scopus (232) Google Scholar This raises the possibility that the virus is subsequently introduced into patients’ eyes via self-inoculation. Therefore, good personal hygiene throughout the disease course would theoretically lower the chance of self-inoculation. In summary, our study found that conjunctival carriage of SARS-CoV-2 is low even in place of standardised sampling technique. This is probably good news for ophthalmic health care workers. Nevertheless, adequate eye protection and stringent personal hygiene are still important as they may contribute to further reduce ocular COVID-19 transmission to minimal. The present study is limited by the lack of a control group to assess the protective and risk factors of viral transmission of COVID-19 via the conjunctiva. Future case-controlled studies and the use of a validated personal hygiene questionnaire8Bin Abdulrahman AK Bin Abdulrahman KA Almadi MK Alharbi AM Mahmoud MA Almasri MS et al.Do various personal hygiene habits protect us against influenza-like illness?.BMC Public Health. 2019; 19: 1324Crossref PubMed Scopus (10) Google Scholar would yield further fruitful findings because there are reports of positive conjunctiva swab for SARS-CoV-2 in the absence of ocular symptoms (Table 1) and vice versa. The relationship between the presence of SARS-CoV-2 on the conjunctiva and ocular symptoms remains to be elucidated. In addition, molecular study also suggested the possibility of the cornea being an ocular site of infection instead of conjunctiva.9Ma D Chen C Jhanji V Xu C Yuan XL Liang JJ et al.Expression of SARS-CoV-2 receptor ACE2 and TMPRSS2 in human primary conjunctival and pterygium cell lines and in mouse cornea.Eye (Lond). 2020; 34: 1212-1219Crossref PubMed Scopus (130) Google Scholar Future larger-scale studies aimed at investigating these issues could provide more insight. The authors have no proprietary or commercial interest in any materials discussed in this article. eyJraWQiOiI4ZjUxYWNhY2IzYjhiNjNlNzFlYmIzYWFmYTU5NmZmYyIsImFsZyI6IlJTMjU2In0.eyJzdWIiOiIzYmVjYjkwMWQ3Yzg0OWRlOTY1ZDZhYWE0ZmFjOGVlMiIsImtpZCI6IjhmNTFhY2FjYjNiOGI2M2U3MWViYjNhYWZhNTk2ZmZjIiwiZXhwIjoxNjc0ODYwNjU0fQ.ENWWS_gsXhRhy56FGUAK3E5cMBVyOPQDqNJAETk6Wa2QE3yxHH0xAEHUQHEEh-5qWU8CvzXPiyQDjqH05Kgez-tQ9y5uFrric-0rLwynyEiCJCRkyqhdkMlf_Ggzc-lCgGOnJ6JzqTlaqv9PrEz4IX5AvxcZbphSUcxrpkWAQamLLVn_FSO45jRC5oTgF099gVp4t_3gT9_cNn2LII3edI_TKCpZHg9jiwb_vpc6cCAcYE0mbol94QFVdeWQOX02L6h1WY9TJonJAr2hBC0fpedccP4uoLWnGKlMRNoG4ErkUCgszHr-1PS70bOn6f-ZO7RIqNeg4mnTRX2BtvJeCg Download .mp4 (9.33 MB) Help with .mp4 files

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