Background: RT-PCR using respiratory tract specimens, most commonly nasopharyngeal swab (NPS), has been used to confirm the diagnosis of COVID-19. NPS is a relatively invasive procedure that causes patient discomfort and risks viral transmission. Other specimens are therefore being investigated for the detection of SARS-CoV-2 RNA. Objective: To determine the sensitivity of non-respiratory tract specimens in detecting SARS-CoV-2 RNA in patients with COVID-19. Methodology: This review summarized the results of eight studies obtained from a literature search done in May 2020 in PubMed MEDLINE, Cochrane Library and MedRxiv. Two independent investigators reviewed and appraised the studies that were included, and pooled estimates of sensitivity for each specimen were determined using Stata’s Metaprop function Results: The sensitivity in detecting SARS-CoV-2 RNA in non-respiratory tract specimens of diagnosed COVID-19 patients are as follows: Saliva 77% (95% CI 71-83%), stool/rectal swab/anal swab 22% (95% CI 22-37%), blood/serum/plasma 2% (95% CI 1-3%), and urine 22% (95% CI 18-25%). Conclusion SARS-CoV-2 RNA is detected in saliva, stool/rectal swab/anal swab, blood/serum/plasma and urine. Among these, saliva has the highest estimated sensitivity. However, more studies are needed to correct the heterogeneity brought about by factors such as timing of specimen collection, disease severity and treatment.
COVID-19

Objective: To present the current evidence on the effect of zinc as adjunct therapy on COVID-19 related outcomes. Methods: A literature search among peer-reviewed, non-peer-reviewed, and guideline practice databases was done until December 26, 2020, with an updated search done on February 13, 2021. Evidence was synthesized among studies that fulfilled the inclusion criteria, and the quality of evidence was determined using GRADEpro. Results: This review used two randomized controlled trials and three retrospective cohort studies. Pooling of the retrospective cohort studies showed that adjunct zinc therapy significantly reduces the risk of mortality or transition to hospice care among COVID-19 patients (OR 0.56, 95% CI 0.38-0.81; I2=p=0.002; very low quality of evidence). However this was not supported by one RCT (N=191) which showed no significant difference in death (RR 0.99, 95% CI, 0.30-3.31; p=0.99], need for mechanical ventilation (RR 0.66, 96% CI, 0.19-2.26; p=0.58] and recovery after 28 days (RR 0.94, 95% CI 0.55-1.62; p=0.83) in patients with COVID-19 given zinc as adjunct treatment together with hydroxychloroquine (HCQ) and azithromycin (AZT) versus HCQ and AZT alone (moderate quality of evidence). A second RCT (N=108) showed no significant difference in the hospitalizations (RR 1.44, 95% CI 0.36, 5.71; p=0.61) and meant several days needed to reach a 50% reduction in symptoms in ambulatory patients with COVID-19 given adjunct zinc gluconate versus standard of care alone (mean difference of -0.80, 95% CI, -2.55-0.95, p=0.37; low quality of evidence). In this study, there were 10 participants in the zinc group with adverse effects, mostly gastrointestinal in origin. Conclusion There is still insufficient evidence to support the use of Zinc as an adjunct therapy in patients with COVID-19 both in inpatient and outpatient settings due to inconsistent benefits and potential adverse effects.
COVID-19 ; Coronavirus ; Zinc