Diabetes and Patient Safety

Objective of Section

To describe the harms that may occur in the delivery of care to patients with diabetes and to present harm prevention and mitigation strategies.

Introduction

In 1999, the Institute of Medicine published the seminal work “To Err is Human,”1 which shed light on the harm created by medical error. In fact, medical error contributes to more than 200,000 deaths per year.2 Over the past 15 years, it has been demonstrated that not all patients and health care settings are at the same risk of having harm occur.3 For multiple reasons, patients with diabetes are at significantly greater risk than most patients. They often have multiple comorbidities and complications that increase their likelihood of using health care services. Additionally, some of the medications used to reduce blood sugar—both oral and injectable agents—carry a risk of hypoglycemia. Therefore, patients with diabetes are at risk for harm from medical errors by individual health care professionals, systems errors by health systems that are poorly designed, and inappropriate actions by patients themselves due to lack of knowledge or skills.

Achieving safe diabetic care requires active attention at all levels. From newer, more physiologic medications, to increasingly advanced monitoring devices, to enhanced systems designs to improve care transitions, diabetic care is receiving the attention that is required from leaders in industry, health care systems, and patients. This section introduces these advances and issues within the patient safety movement as it relates to the patient with diabetes.

References