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From the 1Chair, Professor, Departments of Medicine, Biochemistry Diabetes Research Center, Mountain Brook, Alabama, 13Grunberger Diabetes
and Molecular Biology, and Molecular and Cellular Biology, Baylor Institute, Clinical Professor, Internal Medicine and Molecular Medicine &
College of Medicine, Houston, Texas, 2Beth Israel Deaconess Medical
Center, Department of Medicine and Harvard Medical School, Boston, Michigan, 14Medical Director & Principal Investigator, Metabolic Institute of
Massachusetts, 3Division of Endocrinology, Kaiser Permanente of Georgia America, President, American College of Endocrinology, Tarzana, California,
and the Division of Endocrinology, Emory University School of Medicine, 15Professor of Medicine, University of California San Diego, Chief, Section of
Atlanta, Georgia, 4Director, Ochsner Diabetes Clinical Research Unit, Diabetes, Endocrinology & Metabolism, VA San Diego Healthcare System,
Department of Endocrinology, Diabetes and Metabolism, Ochsner Medical San Diego, California, 16Professor of Medicine, University of Washington
Center, New Orleans, Louisiana, 5Clinical Professor, Mount Sinai School of School of Medicine, Seattle, Washington, 17Professor of Clinical Medicine,
Medicine, Editor, Journal of Diabetes, New York, New York, 6Clinical Chief, University of Miami, Miller School of Medicine, Miami, Florida, The Center
Division of Endocrinology, Cedars-Sinai Medical Center, Associate Clinical for Diabetes & Endocrine Care, Hollywood, Florida, 18Professor of Medicine,
Professor of Medicine, Geffen School of Medicine, UCLA, Los Angeles, Division of Endocrinology, Metabolism & Lipid Research, Washington
California, 7A.C. Mullins Professor & Director, Division of Endocrinology, University, St. Louis, Missouri, 19Clinical Professor of Medicine, Director,
Diabetes and Metabolism, University of Tennessee Health Science Center, Metabolic Support, Division of Endocrinology, Diabetes, and Bone Disease,
Memphis, Tennessee, 8Professor of Medicine, Chief, Diabetes Division, Icahn School of Medicine at Mount Sinai, New York, New York, 20Clinical
University of Texas Health Science Center at San Antonio, San Antonio, Professor, Medicine, Division of Endocrinology, Diabetes, Metabolism,
Texas, 9Immediate Past President, American College of Endocrinology, University California Irvine School of Medicine, Irvine, California,
Past-President, American Association of Clinical Endocrinologists, Co-Director, Diabetes Out-Patient Clinic, UCI Medical Center, Orange,
Medical Director, Scripps Whittier Diabetes Institute, Clinical Professor California, Director & Principal Investigator, Diabetes/Lipid Management
of Medicine, UCSD, Associate Editor, Journal of Diabetes, Diabetes and & Research Center, Huntington Beach, California, and 21Professor of
Endocrine Associates, La Jolla, California, 10Professor of Medicine and Medicine, Emory University School of Medicine, Director, Endocrinology
Pharmacology, Tullis Tulane Alumni Chair in Diabetes, Chief, Section of Section, Grady Health System, Atlanta, Georgia.
Endocrinology, Tulane University Health Sciences Center, New Orleans, Address correspondence to American Association of Clinical
Louisiana, 11Endocrine Division, Harvard Vanguard Medical Associates, Endocrinologists, 245 Riverside Avenue, Suite 200, Jacksonville, FL 32202.
Boston, Massachusetts, Division of Endocrinology, Beth Israel Deaconess E-mail: publications@aace.com. DOI: 10.4158/EP151126.CS
Medical Center, Boston, Massachusetts, 12Professor and Chair, Department To purchase reprints of this article, please visit: www.aace.com/reprints.
of Nutrition Sciences, University of Alabama at Birmingham, Director, UAB Copyright © 2016 AACE.
Abbreviations:
A1C AACE -
ACCORD
ACCORD BP
ACEI
AGI
apo B ARB
ASCVD - (Endocr Pract. 2016;22:84-113)
BAS BMI =
BP CHD = coro- Principles
CKD
CVD DKA -
DPP-4 EPA -
FDA
GLP-1 HDL-C
LDL-C -
LDL-P - -
Look AHEAD
NPH OSA
SFU SGLT-2
SMBG -
T2D TZD =
EXECUTIVE SUMMARY -
-
-
-
-
- -
-
-
-
-
- -
- -
-
Clinical
- Practice Guidelines for Healthy Eating for the Prevention
- and Treatment of Metabolic and Endocrine Diseases in
Adults
-
-
-
Lifestyle Therapy -
-
-
of trans
- -
Drowsiness:
somnolencia
-
-
-
m
- -
Obesity
Prediabetes
- -
-
- -
Solely: solamente
-
-
P
- -
T2D Pharmacotherapy
- -
-
-
-
-
thereby
enhancing:
mejorando
- de este modo
-
- -
- -
- -
- -
-
-
-
-
-
- -
-
-
-
-
- -
-
Insulin
***** -
- -
-
-
-
-
- -
-
-
-
-
-
-
-
-
- -
-
-
- -
onset: inicio
offset: compensar
-
-
-
BP
non-HDL-C:
CT - LDL - TGC/5
CT= total colesterol
TGC/5= VLDL-C
-
-
Lipids
- -
- -
ESTATINAS:
INH de HMG-Co
- reductasa
- -
P -
-
P -
-
-
-
-
- -
-
ACKNOWLEDGMENT
DISCLOSURE
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TABL E OF CONTENTS
Comprehensive Type 2 Diabetes Algorithm
I. Lifestyle Therapy
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LIFE S T YLE THE R A P Y
R I S K S T R ATIFICATION FOR DIA BE TE S COMPLIC AT ION S
+
P Calorie restriction
P Plant-based diet; high polyunsaturated P Structured counseling
Nutrition P Meal replacement
and monounsaturated fatty acids
P Avoid trans fatty acids;
limit saturated fatty acids
+ +
P 150 min/week moderate exertion
P Medical evaluation/
Physical (eg. walking, stair climbing) P Structured
clearance
Activity P Strength training program
P Medical supervision
P Increase as tolerated
Behavioral
Support
P Community engagement
P Screen for mood disorders + P Refer to mental healthcare professional
P Behavioral therapy
Smoking
Cessation
P No tobacco products
+ P Structured programs
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COMPLICATIONSCENTR IC M ODEL FOR CARE
OF THE OV ERWEIG HT/ OBESE PATIENT
S TEP 1 E VA L U AT I O N F O R C O M P L I C AT I O N S A N D S TA G I N G
S TEP 2 SELEC T:
Therapeutic targets for
improvement in complications + Treatment
modality + Treatment intensity based
on staging
If therapeutic targets for complications not met, intensify lifestyle, medical, and/or surgical treatment
S TEP 3 modalities for greater weight loss.
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PREDIABETES ALGORITH M
I FG ( 10 0– 1 2 5 ) | IGT ( 1 4 0– 1 9 9 ) | M E TA B O L IC SYN D RO M E ( N C E P 2 0 0 1 )
LIFESTYLE THERAPY
(Including Medically Assisted Weight Loss)
Orlistat, lorcaserin,
phentermine/topiramate ER, PR OCE E D TO
naltrexone/bupropion, liraglutide 3 mg, HYP E R G LYC E M I A If glycemia
or bariatric surgery as indicated for
ALG OR I T HM not normalized
obesity treatment
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G OA LS FOR G LYCE MIC CON T R OL
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G LYC EMIC CONTR OL A LGORI T HM
LIFESTYLE THERAPY
(Including Medically Assisted Weight Loss)
Entry A1C < 7.5% Entry A1C ≥ 7.5% Entry A1C > 9.0%
MON OT H E R A PY * S YM PTO M S
D UAL T HE R APY*
Metformin NO YE S
GLP-1 RA T R I PL E T HE R APY*
GLP-1 RA
SGLT-2i DUAL INSULIN
SGLT-2i GLP-1 RA
Therapy ±
DPP-4i SGLT-2i Other
DPP-4i
TZD
MET TZD MET TZD
OR Agents
or other or other
TRIPLE
1st-line Basal Insulin 1st-line Basal insulin
AGi Therapy
+
agent agent +
Colesevelam DPP-4i
SU/GLN 2nd-line
+
agent
Bromocriptine QR Colesevelam
AGi Bromocriptine QR
A DD O R I NTENS I FY
SU/GLN AGi I NS UL I N
If not at goal in 3 months
Refer to Insulin Algorithm
SU/GLN
proceed to Dual Therapy If not at goal
in 3 months
proceed to LEGEND
Triple Therapy If not at goal in
3 months proceed Few adverse events and/or
to or intensify possible benefits
insulin therapy
* Order of medications represents a suggested hierarchy of usage; Use with caution
length of line reflects strength of recommendation
P R O G R E S S I O N O F D I S E A S E
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ALG ORITH M FOR ADDING/INTENSIF YING INS ULIN
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A S C V D R I S K FACTOR MODIF ICATIONS ALGORITHM
DYSLIPIDEMIA HYPERTENSION
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PR OF I L E S OF ANTIDIABETIC MEDICATIONS
TZD SU
MET GLP-1 RA SGLT-2i DPP-4i AGi (moderate COLSVL BCR-QR INSULIN PRAML
dose) GLN
Moderate/
Severe Moderate
HYPO Neutral Neutral Neutral Neutral Neutral Neutral Neutral Neutral Neutral
Mild to Severe
Slight
WEIGHT Loss Loss Neutral Neutral Gain Gain Neutral Neutral Gain Loss
Loss
Not
Effective
Contra- Dose
Exenatide with
indicated Adjustment More
RENAL/ Not eGFR < 45 More
CKD Necessary Neutral Neutral Hypo Neutral Neutral Neutral
GU Stage
Indicated
(Except Risk
Hypo Risk
CrCl < 30 Genital
3B,4,5 Linagliptin)
Mycotic
Infections
GI Sx Moderate Moderate Neutral Neutral Moderate Neutral Neutral Mild Moderate Neutral Moderate
Moderate
BONE Neutral Neutral Neutral Neutral Neutral Fracture Neutral Neutral Neutral Neutral Neutral
Risk
Few adverse events or possible benefits Use with caution Likelihood of adverse effects ? Uncertain effect
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PR INC I PL E S OF THE AACE/ACE COMPREHENSIVE
T Y PE 2 DI ABETES M AN AG EM EN T ALGORITHM
1. Lifestyle therapy, including medically supervised weight loss, is key to managing type 2 diabetes.
The choice of therapies must be individualized on basis of patient characteristics, impact of net cost
4. to patient, formulary restrictions, personal preferences, etc.
Initial acquisition cost of medications is only a part of the total cost of care which includes
7. monitoring requirements, risk of hypoglycemia, weight gain, safety, etc.
9. Combination therapy is usually required and should involve agents with complementary actions.
10. Comprehensive management includes lipid and blood pressure therapies and related comorbidities.
11. Therapy must be evaluated frequently until stable (e.g., every 3 months) and then less often.
13. This algorithm includes every FDA-approved class of medications for diabetes.
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