TY - JOUR
T1 - Provider Response to Critical Action Values for Hypoglycemia in the Ambulatory Setting
T2 - a Retrospective Cohort Study
AU - Ashok, Aditya
AU - Abusamaan, Mohammed S.
AU - Parker, Penelope
AU - Pilla, Scott J.
AU - Mathioudakis, Nestoras N.
N1 - Funding Information:
Nestoras Mathioudakis was supported by grant K23DK111986-01 from the National Institute for Diabetes and Digestive and Kidney Diseases. The authors declared that there is no potential conflict of interest.
Publisher Copyright:
© 2020, Society of General Internal Medicine.
PY - 2021/5
Y1 - 2021/5
N2 - Background: The blood glucose level triggering a critical action value (CAV) for hypoglycemia is not standardized, and associated outcomes are unknown. Objective: To evaluate the clinical consequences of, and provider responses to, CAVs for hypoglycemia. Design: Retrospective cohort study at Johns Hopkins Hospital and Johns Hopkins Bayview Medical Center between April 1, 2013, and January 31, 2017. Participants: Patients with an ambulatory serum glucose < 50 mg/dL. Point-of-care capillary glucose and whole blood glucose samples were excluded. Main Measures: Electronic medical record (EMR) review for providers’ documented response to CAV, associated patient symptoms, and serious adverse events. Key Results: We analyzed 209 CAVs for hypoglycemia from 154 patients. The median age (IQR) was 59 years (46, 69), 89 (57.8%) were male, and 96 (62.3%) were black. Provider-to-patient contact occurred in 128 of 209 (61.2%) episodes, among which no documented etiology was observed for 81 of 128 (63.3%), no recommendations were provided in 32 of 128 (25.0%), and no patient-reported hypoglycemic symptoms were documented in 103 of 128 (80.5%). Serious adverse events were documented in 4 of 128 episodes (3.1%), two required glucagon administration, and three required an ED visit. Provider-to-patient contact was associated with the patient having malignant neoplasm (adjusted OR 3.63, p = 0.045) or a hypoglycemic disorder (adjusted OR 7.70, p = 0.018) and inversely associated with a longer time from specimen collection to EMR result (adjusted OR 0.90 per hour, p = 0.016). Conclusions: There is inconsistent provider-to-patient contact following CAVs for hypoglycemia, and the etiology and symptoms of hypoglycemia were infrequently documented. There were few serious documented adverse events associated with hypoglycemia, although undocumented events may have occurred, and the incidence of serious adverse events in non-contacted patients remains unknown. These findings demonstrate a need to standardize provider response to CAVs for hypoglycemia. Decreasing the lag time between sample collection and laboratory result reporting may increase provider-to-patient contact.
AB - Background: The blood glucose level triggering a critical action value (CAV) for hypoglycemia is not standardized, and associated outcomes are unknown. Objective: To evaluate the clinical consequences of, and provider responses to, CAVs for hypoglycemia. Design: Retrospective cohort study at Johns Hopkins Hospital and Johns Hopkins Bayview Medical Center between April 1, 2013, and January 31, 2017. Participants: Patients with an ambulatory serum glucose < 50 mg/dL. Point-of-care capillary glucose and whole blood glucose samples were excluded. Main Measures: Electronic medical record (EMR) review for providers’ documented response to CAV, associated patient symptoms, and serious adverse events. Key Results: We analyzed 209 CAVs for hypoglycemia from 154 patients. The median age (IQR) was 59 years (46, 69), 89 (57.8%) were male, and 96 (62.3%) were black. Provider-to-patient contact occurred in 128 of 209 (61.2%) episodes, among which no documented etiology was observed for 81 of 128 (63.3%), no recommendations were provided in 32 of 128 (25.0%), and no patient-reported hypoglycemic symptoms were documented in 103 of 128 (80.5%). Serious adverse events were documented in 4 of 128 episodes (3.1%), two required glucagon administration, and three required an ED visit. Provider-to-patient contact was associated with the patient having malignant neoplasm (adjusted OR 3.63, p = 0.045) or a hypoglycemic disorder (adjusted OR 7.70, p = 0.018) and inversely associated with a longer time from specimen collection to EMR result (adjusted OR 0.90 per hour, p = 0.016). Conclusions: There is inconsistent provider-to-patient contact following CAVs for hypoglycemia, and the etiology and symptoms of hypoglycemia were infrequently documented. There were few serious documented adverse events associated with hypoglycemia, although undocumented events may have occurred, and the incidence of serious adverse events in non-contacted patients remains unknown. These findings demonstrate a need to standardize provider response to CAVs for hypoglycemia. Decreasing the lag time between sample collection and laboratory result reporting may increase provider-to-patient contact.
KW - Ambulatory
KW - Critical action value
KW - Glucose
KW - Hypoglycemia
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U2 - 10.1007/s11606-020-06225-y
DO - 10.1007/s11606-020-06225-y
M3 - Article
C2 - 32935316
AN - SCOPUS:85091108901
SN - 0884-8734
VL - 36
SP - 1244
EP - 1249
JO - Journal of general internal medicine
JF - Journal of general internal medicine
IS - 5
ER -