Professional Society Guidelines

Professional societies have continued to expand their recommendation of continuous glucose monitoring (CGM) use in patient care protocols for adult and pediatric patients with type 1 or type 2 diabetes.

Resources

American Association of Clinical Endocrinology (AACE) Clinical Practice Guidelines

The Use of Advanced Technology in Management of Persons with Diabetes 2021 The American Association of Clinical Endocrinology (AACE) conducted literature searches for relevant articles published from...

Professional Society Guidelines

Improving the Clinical Value and Utility of CGM Systems: Issues and Recommendations

A Joint Statement of the European Association for the Study of Diabetes and the American Diabetes Association Diabetes Technology Working Group Petrie J, et al. Improving the Clinical Value and...

Professional Society Guidelines

Glucose management for exercise using continuous glucose monitoring (CGM) and intermittently scanned CGM (isCGM) systems in type 1 diabetes

Exercise is vital for managing type 1 diabetes, but it can disrupt glucose levels, leading to fears of hypoglycemia. Utilizing intermittently scanned CGM (isCGM) and continuous glucose monitoring (CGM...

Professional Society Guidelines

American Diabetes Association Standards of Medical Care in Diabetes—2022

Title: “Chapter 7: Diabetes Technology: Standards of Medical Care in Diabetes - 2022.” Journal: Diabetes Care; 45(Suppl. 1):S97–S112, 2022 | https://doi.org/10.2337/dc22-S007 Author: American Diabetes...

Professional Society Guidelines

Endocrine Society Dosing Method Based on CGM Trend Arrows and CF

The Endocrine Society recently published new diabetes treatment guidelines, 1,2 which may help providers to guide patients on adjusting pre-meal and ≥3 hour post-meal insulin doses using Dexcom G5...

Professional Society Guidelines

Diabetes Technology: Standards of Medical Care in Diabetes—2021

American Diabetes Association 7. Diabetes Technology: Standards of Medical Care in Diabetes—2021. Diabetes Care. 2021; 44 (1): S85-S99.

Professional Society Guidelines

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By submitting the above form, I certify that I am a licensed practitioner, authorized to receive and dispense samples of the Dexcom G6 Continuous Glucose Monitoring System and/or Dexcom‘s next generation product, Dexcom G7 (the "Samples"). I represent that I am requesting the Samples for evaluation purposes and that I will not (i) sell, resell, barter, return for credit or seek reimbursement for the use of the Samples, or (ii) for professional services for dispensing or evaluating the Samples, I also agree to inform my patients that they should not submit claims for reimbursement to any third party for any Samples.

The Samples are FDA cleared for use with a compatible smart device or separate piece of durable medical equipment called a receiver. Neither devices nor receivers are included in the Samples. Accordingly, and in light of the applicable G6 or G7 Dexcom Instructions for Use, you should dispense Samples only to a patient who (or whose authorized caregiver), in the exercise of your clinical judgment, (i) has reliable access to a compatible smart device and/or automated insulin delivery system, and (ii) is capable of safely using the Samples with their smart device, without the need for a separate dedicated receiver.

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