| Literature DB >> 34338994 |
Thomas Danne1, Catarina Limbert2,3, Manel Puig Domingo4, Stefano Del Prato5, Eric Renard6,7, Pratik Choudhary8,9, Alexander Seibold10.
Abstract
People with diabetes are at greater risk for negative outcomes from COVID-19. Though this risk is multifactorial, poor glycaemic control before and during admission to hospital for COVID-19 is likely to contribute to the increased risk. The COVID-19 pandemic and restrictions on mobility and interaction can also be expected to impact on daily glucose management of people with diabetes. Telemonitoring of glucose metrics has been widely used during the pandemic in people with diabetes, including adults and children with T1D, allowing an exploration of the impact of COVID-19 inside and outside the hospital setting on glycaemic control. To date, 27 studies including 69,294 individuals with T1D have reported the effect of glycaemic control during the COVID-19 pandemic. Despite restricted access to diabetes clinics, glycaemic control has not deteriorated for 25/27 cohorts and improved in 23/27 study groups. Significantly, time in range (TIR) 70-180 mg/dL (3.9-10 mmol/L) increased across 19/27 cohorts with a median 3.3% (- 6.0% to 11.2%) change. Thirty per cent of the cohorts with TIR data reported an average clinically significant TIR improvement of 5% or more, possibly as a consequence of more accurate glucose monitoring and improved connectivity through telemedicine. Periodic consultations using telemedicine enables care of people with diabetes while limiting the need for in-person attendance at diabetes clinics. Reports that sustained hyperglycaemia and early-stage diabetic ketoacidosis may go untreated because of the lockdown and concerns about potential exposure to the risk of infection argue for wider access to glucose telemonitoring. Therefore, in this paper we have critically reviewed reports concerning use of telemonitoring in the acute hospitalized setting as well as during daily diabetes management. Furthermore, we discuss the indications and implications of adopting telemonitoring and telemedicine in the present challenging time, as well as their potential for the future.Entities:
Keywords: Ambulatory glucose profile; COVID-19; Continuous glucose monitoring; Diabetes; Insulin pumps; Mortality; Risk management; Telemedicine; Telemonitoring; Virtual care
Year: 2021 PMID: 34338994 PMCID: PMC8327601 DOI: 10.1007/s13300-021-01114-x
Source DB: PubMed Journal: Diabetes Ther ISSN: 1869-6961 Impact factor: 2.945
Fig. 1Risk matrix for people during the COVID-19 pandemic. Summary of the known risk factors for infection and disease severity with COVID 19. eGFR estimated glomerular filtration rate (ml/min/1.73 m2), T1D type 1 diabetes, T2D type 2 diabetes
Studies reporting glycaemic metrics before and during COVID-19 social lockdown
| Study | Region | Adults/children ( | Type | System | Change in glycaemic metrics |
|---|---|---|---|---|---|
| Bonora BM [ | Italy | Adults (33) | T1D | FreeStyle Libre | AG, mg/dL 177–160 ( %TIR 54–65.2 ( %TAR1 42.3–31.6 ( SD, mg/dL 58.9–53.2 ( |
| Capaldo B [ | Italy | Adults (207) | T1D | FreeStyle Libre ( Medtronic Guardian ( Dexcom G6 ( Eversense ( | %TIR 55.6–58.2 ( %TBR2 1.42–0.58 ( %CV 35.9–34.7 ( |
| Schiaffini R [ | Italy | Children (22) | T1D | Dexcom G6 | %TIR 61.45–66.41 ( %TAR1 34.73–29.86 ( TDD, IU/day 7.9–5.3 ( |
| Christoforidis A [ | Greece | Children (34) | T1D | Medtronic Enlite | %CV 39.5–37.4 ( |
| Fernández E [ | Spain | Adults (307) | T1D | FreeStyle Libre | AG, mg/dL 167–158 ( %TIR 57.8–62.5 ( %TBR1 4.9–5.5 ( %TAR1 37.3–32.0 ( eA1c 7.4–7.1 ( |
| Mesa A [ | Spain | Adults (92) | T1D | Free Style Libre ( Dexcom G5 ( | %TIR 59.3–62.6 ( %TAR1 34.4–30.7 ( GMI, % 7.2–7.0 ( |
| Cotovad-Bellas L [ | Spain | Adults (44) | T1D | FreeStyle Libre | No change during lockdown |
| Caruso I [ | Italy | Adults (48) | T1D | FreeStyle Libre | %TBR1 6.3–4.5 ( %CV 38.3–35.1 ( |
| Aragona M [ | Italy | Adults (63) | T1D | FreeStyle Libre ( Dexcom G6 ( | AG, mg/dL 165–158 ( %TIR 58–61 ( %TAR1 38–34 ( GMI, % 7.2–7.0 ( |
| Dover AR [ | UK | Adults (572) | T1D | FreeStyle Libre | AG, mmol/L 9.6–9.3 ( %TIR 53–56 ( %TBR 3−3 ( %TAR1 42–39 ( eA1c 61–58 ( |
| Di Dalmazi G [ | Italy | Children ≤ 12 years (30) | T1D | Freestyle Libre ( Dexcom G5 or G6 ( | SD 67.4–64.3 ( |
| Di Dalmazi G [ | Italy | Teenagers 13–17 years (24) | T1D | Freestyle Libre ( Dexcom G5 or G6 ( | No change during lockdown |
| Di Dalmazi G [ | Italy | Adults (76) | T1D | Freestyle Libre ( Dexcom G5/G6 ( | AG, mg/dL 164–160 ( %TIR 57.7–61.3 ( %TBR1 2.5–3.0 ( %TAR1 26.5–25.1 ( %TAR2 11.1–7.8 ( SD 63.0–59.6 ( eA1c, % 7.2–6.8 ( GMI,% 7.7–7.6 ( |
| Brener A [ | Israel | Children (102) | T1D | Dexcom G5 | No change during lockdown |
| Pla B [ | Spain | Adults (50) | T1D | FreeStyle Libre | AG, mg/dL 160.3–150.0 ( %TIR 57.5–65.8 ( %CV 40.7–36.4 ( eA1c, % 7.2–6.8 ( GMI,% 7.2–6.9 ( |
| Prabhu Navis J [ | UK | Adults (269) | T1D | Freestyle Libre ( Dexcom G6 ( | %TIR 57.5–59.6 ( %CV 37–36 ( |
| Barchetta I [ | Italy | Adults (50) | T1D | FreeStyle Libre and other CGM, unspecified | AG, mg/dL 154–165 ( %TIR 75–69 ( %TBR1 6–10 ( eA1c 7.3–7.5 ( |
| Predieri B [ | Italy | Children (62) | T1D | Dexcom G6 | %TIR 60.0–62.1 ( %TAR1 37.8–35.7 ( %TBR1 2.63–2.13 ( %TBR2 0.5–0.34 ( |
| Braune K [ | Germany | Children (28) | T1D | Freestyle Libre ( Dexcom G5/G6 ( Medtronic Guardian ( | %TIR 46.9–56.3 ( %TAR1 21.3–13.9 ( |
| Potier L [ | France | Adults (1378) | T1D | FreeStyle Libre | AG, mmol/L 9.1–8.7 ( |
| Boscari F [ | Italy | Adults (79) | T1D | FreeStyle Libre ( Dexcom ( Other CGM ( | AG, mg/dL 161.1–156.3 ( %TIR 63.6–66.3 ( %TAR1 33.4–30.5 ( |
| Sánchez Conejero M [ | Spain | Children (80) | T1D | FreeStyle Libre ( Medtronic Guardian ( Dexcom G6 ( | %TIR 72.1–74.8 ( %TAR2 4.6–3.7 ( %TBR1 4.6–3.2 ( %TBR2 1.2–0.7 ( %CV 35.8–33.1 ( |
| Rachmiel M [ | Israel | Children (195) | T1D | Unspecified CGM | AG, mg/dL 164–160 ( %TIR 59–63 ( %TAR1 32.0–38.6 ( %CV 37.1–35.6 ( eA1c, % 7.35–7.20 ( |
| Marigliano M [ | Italy | Children (233) | T1D | FreeStyle Libre ( Dexcom G6 ( SMBG ( | AG, mg/dL 178.6–169.1 ( %TIR 52.6–58.0 ( %TAR1 43.4–38.0 ( SD 68.0–63.6 ( GMI, % 7.60–7.37 (p < 0.001) |
| Alharthi SK [ | Saudi Arabia | Adults (101) | T1D | Unspecified CGM | AG, mg/dL 180–159 ( %TIR 46–55 ( %TAR1 48–35 ( GMI,% 7.7–7.2 ( |
| van der Linden J [ | USA | NA (65,067) | All | Dexcom G6 | %TIR 59–61 ( |
| Viñals C [ | Spain | Adults (59) | T1D | Medtronic 640G + Enlite | AG, mg/dL 153.2–147.8 ( %TIR 67.6–69.8 ( eA1c, % 6.94–6.75 (p < 0.001) |
Studies are listed in date order as disclosed on PubMed. Significant changes in glycaemic metrics from before to during COVID-19 lockdown are presented. Each number sequence indicates change from before to during lockdown with p value
AG average glucose, eA1c estimated HbA1c, %CV % coefficient of mean glucose, GMI glucose management indicator, %TIR percentage time in range 70–180 mg/dL (3.9–10 mmol/L), %TBR1 percentage time below range < 70 mg/dL (3.9 mmol/L), %TBR2 percentage time below range < 54 mg/dL (3.0 mmol/L), %TAR1 percentage time above range > 180 mg/dL (10 mmol/L), %TAR1 percentage time above range > 250 mg/dL (13.8 mmol/L), TDD total daily dose of bolus insulin, NA no information about demogaphics
Box 1. Definitions for Telemedicine and Telemonitoring in Context of Diabetes Care
| Telemedicine | Managing diabetes care using telecommunications technology, including telephone and video conferencing, to deliver care at a distance. In this way, a healthcare professional (HCP) in one location can provide a medical consultation, including treatment adjustment, to a patient at a distant site. Telemedicine can also involve multiple HCPs in a synchronous patient consultation or care review. |
| Telemonitoring | The use of diabetes-specific medical devices that can monitor, transmit and share indicators of diabetes health between a person with diabetes and their diabetes care team. Telemonitoring allows care of patients at home or at other locations remote from their HCPs, using mobile phones, tablet computers, and desktop computers. Telemonitoring allows information, such as interstitial glucose readings from CGM systems, to be stored and reviewed by separate members of the diabetes care team, including the patient. |
Fig. 2Hyperglycaemic risk profiles for COVID-related disease and mortality. ¶For HbA1c < 7.5% (58 mmol/mol) [37]. *For HbA1c ≥ 7.6% (60 mmol/mol) [4]. Risk profiles compared to HbA1c < 7.0% (53 mmol/mol). Data derived from relative risk [4], hazard ratio [37] or odds ratio [36] assessments. Risk factors categorized by separate diabetes type indicated on the bars only where known
| Despite restricted access to standard clinical care during the COVID-19 pandemic, glycaemic control has not deteriorated for people with type 1 diabetes using telemonitoring of glucose data. |
| The increased risk profile for severe COVID-19 disease on hospital admission for people with diabetes can be mitigated by application of telemonitoring and glucose-lowering treatment immediately following admission. |
| Routine telemonitoring can identify groups of at-risk individuals with diabetes who need in-person consultation and care, as well as those who may be successfully managed with telemedicine. |
| The COVID-19 pandemic has highlighted the unmet need for wider application of telemedicine and telemonitoring via CGM for people with diabetes, including those with hyperglycaemia and early-stage diabetic ketoacidosis that may go untreated during times of restricted clinical access. |
| The efficacy of diabetes digital health ecosystems has been validated during the COVID-19 public health emergency and argues for accelerated implementation of these models of care in diabetes. |