Table 2.
Limitations of AID systems
| Physiological | |
| 1. Time lag in sensor glucose values as measured in ISF vs blood | |
| 2. Delayed absorption of insulin from subcutaneous depot; pharmacodynamic effects of applied insulin are different from physiological secreted insulin | |
| Technological | |
| 1. Suboptimal analytical accuracy of CGM systems in low glucose range | |
| 2. Compression of tissue around sensor insertion site leads to falsely detected hypoglycaemia | |
| 3. Missing sensor glucose data (e.g., due to transmission failures) and sensor warm-up time | |
| 4. Glucose sensor overreading and inadvertent overdelivery of insulin | |
| 5. Infusion set failures or pod failure | |
| 6. Outright pump failure due to software or hardware issues | |
| 7. Issues with data uploading, regular exchange of batteries, loss of communication between components of the AID system/cloud network | |
| 8. Server interruptions leading to inability to remotely track data | |
| 9. Cybersecurity/data protection/data privacy | |
| 10. Need for regular update of software/operating systems/apps | |
| 11. Impact of work or environmental conditions has to be considered (i.e., exposure to high or low temperatures, magnetic fields, or water) | |
| Behavioural | |
| 1. Patient needs to bolus prandial insulin | |
| 2. Requirement of correction boluses | |
| 3. Problem-solving for hyperglycaemia (i.e., detect failed infusion sets, broken system components) | |
| 4. Avoidance of hyperglycaemia overcorrections and avoiding adding fake carbs, etc. | |
| 5. Overtreatment of hypoglycaemia | |
| 6. Limitations and challenges of exercise | |
| 7. Need for backup supplies |