Continuous glucose monitoring to assess glycemic control in the first 6 weeks after pancreas transplantation.


Journal

Clinical transplantation
ISSN: 1399-0012
Titre abrégé: Clin Transplant
Pays: Denmark
ID NLM: 8710240

Informations de publication

Date de publication:
10 2019
Historique:
received: 20 05 2019
revised: 31 08 2019
accepted: 12 09 2019
pubmed: 24 9 2019
medline: 22 9 2020
entrez: 24 9 2019
Statut: ppublish

Résumé

Current therapy for Type 1 diabetes (T1D) is characterized by significant glucose variability (GV). Pancreas transplantation (PT) is performed in certain T1D patients with and without end-stage renal disease. To date, GV has been examined to a limited extent after PT. We investigated GV using continuous glucose monitoring (CGM) 3-6 weeks after PT. Eleven patients had simultaneous kidney pancreas transplantation (SPK), nine pancreas after kidney (PAK), and six pancreas transplantation alone (PTA). Mean CGM showed no difference between SPK, 126.5 ± 13.9, PAK 119.9 ± 12.8, and PTA 131.1 ± 29 mg/dL (P value .6). Percentage of time in range (TIR, 70-180 mg/dL) was 92% for SPK, 93.4% in PAK, and 88.5% in PTA with only 0.3%, 1.5%, and 0.3% of time <70 mg/dL. Percentage >180 mg/dL was 7.9% for SPK, 4.9% PAK, and 11% in PTA. Other measures of GV were similar in the three cohorts. In six patients, CGM was performed before and after PT and improved significantly. GV was also better compared with a matched cohort of T1D patients. All 3 types of PT resulted in excellent glucose control 3-6 weeks post-procedure. CGM outcomes represent an important objective outcome after PT.

Sections du résumé

BACKGROUND
Current therapy for Type 1 diabetes (T1D) is characterized by significant glucose variability (GV). Pancreas transplantation (PT) is performed in certain T1D patients with and without end-stage renal disease. To date, GV has been examined to a limited extent after PT.
METHODS
We investigated GV using continuous glucose monitoring (CGM) 3-6 weeks after PT.
RESULTS
Eleven patients had simultaneous kidney pancreas transplantation (SPK), nine pancreas after kidney (PAK), and six pancreas transplantation alone (PTA). Mean CGM showed no difference between SPK, 126.5 ± 13.9, PAK 119.9 ± 12.8, and PTA 131.1 ± 29 mg/dL (P value .6). Percentage of time in range (TIR, 70-180 mg/dL) was 92% for SPK, 93.4% in PAK, and 88.5% in PTA with only 0.3%, 1.5%, and 0.3% of time <70 mg/dL. Percentage >180 mg/dL was 7.9% for SPK, 4.9% PAK, and 11% in PTA. Other measures of GV were similar in the three cohorts. In six patients, CGM was performed before and after PT and improved significantly. GV was also better compared with a matched cohort of T1D patients.
CONCLUSIONS
All 3 types of PT resulted in excellent glucose control 3-6 weeks post-procedure. CGM outcomes represent an important objective outcome after PT.

Identifiants

pubmed: 31545535
doi: 10.1111/ctr.13719
doi:

Substances chimiques

Blood Glucose 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13719

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK088791
Pays : United States

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Vikash Dadlani (V)

Division of Endocrinology, Mayo Clinic, Rochester, Minnesota.

Ravinder Jeet Kaur (RJ)

Division of Endocrinology, Mayo Clinic, Rochester, Minnesota.

Mark Stegall (M)

Department of Transplant Surgery, Mayo Clinic Rochester, Rochester, Minnesota.

Souzana-Eirini Xyda (SE)

Division of Endocrinology, Mayo Clinic, Rochester, Minnesota.

Kanchan Kumari (K)

Division of Endocrinology, Mayo Clinic, Rochester, Minnesota.

Keisha Bonner (K)

Department of Transplant Surgery, Mayo Clinic Rochester, Rochester, Minnesota.

Byron Smith (B)

Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.

Prabin Thapa (P)

Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.

Patrick G Dean (PG)

Department of Transplant Surgery, Mayo Clinic Rochester, Rochester, Minnesota.

Yogish C Kudva (YC)

Division of Endocrinology, Mayo Clinic, Rochester, Minnesota.

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