SlideShare a Scribd company logo
1 of 16
ACCORD
The ACCORD Study Group. “Effects of intensive
glucose lowering in Type 2 Diabetes” New England
Journal of Medicine. 2008. 358(24):2545-59.
SUMMARIZED BY MARIA MORKOS
Action to Control Cardiovascular Risk in Diabetes (ACCORD)
Summarized by: Maria Morkos, MD; Laxmi Suthar, MD
BACKGROUND
 Research has shown that in T2DM
patients, a relationship exists
between A1c levels and CV events
 No previous study has investigated
if intensive therapy to target normal
A1c levels would decrease CV events
in T2DM patients who had CV
disease/risk factors
CLINICAL QUESTION
Would a therapeutic strategy targeting normal A1c
levels
(below 6% vs targeting A1c levels of 7.0-7.9%)
reduce the rate of cardiovascular events in T2DM
persons with established cardiovascular disease
and/or additional cardiovascular risk factors?
DESIGN
 Analysis: chi square tests and two-sample t-tests
 77 clinical centers across the US and Canada
 N = 10,251
 Group 1: received intensive therapy targeting an A1c of less than 6.0%
 Group 2: received standard therapy targeting an A1c of 7.0 to 7.9%
 Follow-up was 3.5 years (intensive therapy was discontinued after higher mortality was found
in the intensive therapy group)
 Primary outcomes:
 first occurrence of nonfatal MI or stroke
 or death from CV causes (MI, HF, stroke, CV cause of death after non-cardiovascular surgery)
 Secondary outcome: death from any cause
POPULATION
Inclusion Criteria
 T2DM and A1c of 7.5% or higher
 ages 40-79 yo
 CV disease or between 55-79 yo and had
anatomical evidence of significant
atherosclerosis, albuminuria, LVH, or at
least 2 additional risk factors for CV
disease (dyslipidemia, HTN, currently
smoking, obesity)
Exclusion Criteria
 Frequent or recent serious hypoglycemic
events
 Unwillingness to do home glucose
monitoring or inject insulin
 BMI > 45
 Serum Cr of > 1.5
 Or other serious illness
INTERVENTIONS
 Group 1
 received intensive therapy targeting A1c of less than 6.0%
 attended monthly visits for the first 4 months then q2 months after that, with at least one interim
phone call
 Group 2 (Placebo Control)
 received standard therapy targeting A1c of 7.0 to 7.9%
 glycemic management visits q4 months
 All patients received study formulary meds as well as glucose monitoring supplies
 Any marketed anti-hyperglycemic therapy that was not provided by formulary could also be prescribed
but was not provided by study investigators
 Also received instructional materials and behavioral counseling regarding diabetes
 Therapeutic regimens were individualized at investigators’ and patients’ discretion based on
study-group assignment and response to therapy
INTERVENTIONS (CONT’D)
 Glucose lower drugs included: metformin, secretagogues, thiazolidinediones, an alpha
glucosidase inhibitor, incretin, insulin
 In addition…
 4733 patients were randomly assigned to lower their BP by receiving either intensive
therapy (SBP target <120) or standard therapy (SBP target <140)
 5518 patients were randomly assigned, while on simvastatin, to either fenofibrate or
placebo
 At time of study publication, BP and lipid trials were still continuing
RESULTS
 At 1 year and after, throughout the follow-up period,
 median A1c for intensive therapy group was 6.4%
 median A1c for standard therapy group was 7.5%
 The intensive therapy group had significantly higher rates of:
 hypoglycemia (requiring assistance)
 weight gain (>10 kg)
 and fluid retention
 The intensive therapy group had a lower rate of nonfatal MI BUT higher rate of
death from CV causes; no significant difference in rates of nonfatal stroke
 Rate of death from any cause was HIGHER in the intensive therapy group
CRITICISMS/LIMITATIONS
 Did not study the components of the intervention strategies used
 Did not address an optimal rate to lower glucose levels
 Glucose lowering strategies were adjusted for each patient in an open fashion
based on their glycemic response to a drug/drug combination and the
development of clinical sx such as hypoglycemia
 No clear explanation for higher mortality found in intensive therapy group
 ?Application to T2DM patients with A1c lower than 7.5% or T2DM patients w/o
CV history or risk factors
 Benefits from intensive glucose lowering therapy may need more than 3.5
years to emerge
BOTTOM LINE
Therapeutic targeting of A1c
levels below 6.0% INCREASED the
rate of death from any cause after
a mean of 3.5 years,
as compared with a strategy
targeting levels of 7.0-7.9%
In patients with a median A1c 8.1%
and previous CV events/multiple CV
risk factors
DISCUSSION QUESTIONS
 What are two important inclusion criteria for the diabetic population this trial
targeted?
 What were the target A1c levels of the two different therapy groups?
 What was the outcome discovered after ~3 years of the trial?
DISCUSSION ANSWERS
 What are two important facts about the patient population this trial targeted?
 ANSWER: Had A1c greater than 7.5% and had to have either a CV event in past or several
CV risk factors
 What were the target A1c levels of the two different therapy groups?
 ANSWER: intensive therapy group target was A1c < 6.0%; standard therapy group target
was A1c 7.0-7.9%
 What was the outcome discovered after ~3 years of the trial?
 ANSWER: intensive therapy to target lower A1c levels (<6.0%) increased mortality and
did not significantly reduce major cardiovascular events
BOARD-LIKE QUESTION
43 yo M is evaluated during a follow-up visit
for management of T1DM. Pt has had
multiple complications including ESRD,
gastroparesis, frequent hypoglycemia with
hypoglycemic unawareness, painful
neuropathy, and proliferative retinopathy.
He uses an insulin pump and checks
fingerstick glucoses several times during the
day, which range from 65 to 250. Most
recent A1c is 7.5%
(Adapted from MKSAP 17)
QUESTION
Which of the following is the most
appropriate next step in the management of
this patient?
A. Alter insulin pump settings to attain an
A1c of less than 7.0%
B. Alter insulin pump settings to decrease
the insulin doses
C. Discontinue the insulin pump, start
subQ insulin injections
D. Start gabapentin for treatment of painful
peripheral neuropathy
BOARD-LIKE QUESTION
Educational Objective:
Liberalize glycemic targets in a patient with
multiple diabetic complications and
advanced microvascular disease
Key Point:
- Frequent hypoglycemia/hypoglycemic
unawareness increases the risk of
morbidity and mortality
- A less stringent A1c goal (such as 8%, per
the ADA) is appropriate for persons with
DM with a decreased life expectancy,
history of severe hypoglycemia, multiple
comorbidities, or advanced
micro/macrovascular disease
QUESTION
Which of the following is the most appropriate
next step in the management of this patient?
A. Alter insulin pump settings to attain an A1c
of less than 7.0%
B. Alter insulin pump settings to decrease the
insulin doses
C. Discontinue the insulin pump, start subQ
insulin injections
D. Start gabapentin for treatment of painful
peripheral neuropathy
REFERENCES
 Effects of intensive glucose lowering in Type 2 Diabetes (2008). New England Journal of Medicine,
358:2545.-2559. doi 10.1056/NEJMoa0802743

More Related Content

What's hot

Screening for asymptomatic cad in diabetes
Screening for asymptomatic cad in diabetesScreening for asymptomatic cad in diabetes
Screening for asymptomatic cad in diabetes
Shyam Jadhav
 
Hyper tension and diabetes the two terrorists together
Hyper tension and diabetes the two terrorists together Hyper tension and diabetes the two terrorists together
Hyper tension and diabetes the two terrorists together
Kyaw Win
 
Diabetic nephropathy management
Diabetic nephropathy managementDiabetic nephropathy management
Diabetic nephropathy management
Naresh Monigari
 

What's hot (20)

Management of Diabetes.pptx
Management of Diabetes.pptxManagement of Diabetes.pptx
Management of Diabetes.pptx
 
Management of hypertriglyceredemia newer update
Management of hypertriglyceredemia newer updateManagement of hypertriglyceredemia newer update
Management of hypertriglyceredemia newer update
 
Hypertensive Dyslipidaemics
Hypertensive DyslipidaemicsHypertensive Dyslipidaemics
Hypertensive Dyslipidaemics
 
Prediabetes
PrediabetesPrediabetes
Prediabetes
 
Sglt2 inhibitors past present and future
Sglt2 inhibitors past present and futureSglt2 inhibitors past present and future
Sglt2 inhibitors past present and future
 
dyslipidemia6.ppt
dyslipidemia6.pptdyslipidemia6.ppt
dyslipidemia6.ppt
 
Management of dyslipidemia
Management of dyslipidemiaManagement of dyslipidemia
Management of dyslipidemia
 
Dyslipidemia by dr. topu
Dyslipidemia by dr. topuDyslipidemia by dr. topu
Dyslipidemia by dr. topu
 
Screening for asymptomatic cad in diabetes
Screening for asymptomatic cad in diabetesScreening for asymptomatic cad in diabetes
Screening for asymptomatic cad in diabetes
 
Hyper tension and diabetes the two terrorists together
Hyper tension and diabetes the two terrorists together Hyper tension and diabetes the two terrorists together
Hyper tension and diabetes the two terrorists together
 
Diabetic dyslipidemia
Diabetic dyslipidemiaDiabetic dyslipidemia
Diabetic dyslipidemia
 
Diabetic Dyslipidemia- Dr Shahjada Selim
Diabetic Dyslipidemia- Dr Shahjada SelimDiabetic Dyslipidemia- Dr Shahjada Selim
Diabetic Dyslipidemia- Dr Shahjada Selim
 
JOURNAL CLUB (2) (1) (3) (5) (1).pptx
JOURNAL CLUB (2) (1) (3) (5) (1).pptxJOURNAL CLUB (2) (1) (3) (5) (1).pptx
JOURNAL CLUB (2) (1) (3) (5) (1).pptx
 
Prediabetes -a brief medical study
Prediabetes -a brief medical studyPrediabetes -a brief medical study
Prediabetes -a brief medical study
 
What’s new in Lipidology, Lessons from “recent guidelines“
What’s new in Lipidology, Lessons from “recent guidelines“What’s new in Lipidology, Lessons from “recent guidelines“
What’s new in Lipidology, Lessons from “recent guidelines“
 
Diabetic nephropathy management
Diabetic nephropathy managementDiabetic nephropathy management
Diabetic nephropathy management
 
ADA GUIDELINE.pptx
ADA GUIDELINE.pptxADA GUIDELINE.pptx
ADA GUIDELINE.pptx
 
SGLT2I The paradigm change in diabetes management
SGLT2I The paradigm change in diabetes managementSGLT2I The paradigm change in diabetes management
SGLT2I The paradigm change in diabetes management
 
Dapagliflozin Ib CKD.pptx
Dapagliflozin Ib CKD.pptxDapagliflozin Ib CKD.pptx
Dapagliflozin Ib CKD.pptx
 
Sglt2i Empagliflogin canagliflogin dapagliflogin- beyond glycemic control
Sglt2i Empagliflogin canagliflogin dapagliflogin- beyond glycemic controlSglt2i Empagliflogin canagliflogin dapagliflogin- beyond glycemic control
Sglt2i Empagliflogin canagliflogin dapagliflogin- beyond glycemic control
 

Similar to ACCORD

Hb a1c goals
Hb a1c goalsHb a1c goals
Hb a1c goals
Daniel Wu
 
Ueda2015 sanofi insulin therapy dr.khaled el-hadidy
Ueda2015 sanofi insulin therapy dr.khaled el-hadidyUeda2015 sanofi insulin therapy dr.khaled el-hadidy
Ueda2015 sanofi insulin therapy dr.khaled el-hadidy
ueda2015
 
SPRINT BP Journal club
SPRINT BP Journal clubSPRINT BP Journal club
SPRINT BP Journal club
Michael Nguyen
 

Similar to ACCORD (20)

Hb a1c goals
Hb a1c goalsHb a1c goals
Hb a1c goals
 
UKPDS
UKPDSUKPDS
UKPDS
 
RSSDI
RSSDI RSSDI
RSSDI
 
DCCT
DCCTDCCT
DCCT
 
What after metformin ?
What after metformin ? What after metformin ?
What after metformin ?
 
Slides to Guide Reducing Cardiovascular Risk in Type 2 Diabetes: What I Do an...
Slides to Guide Reducing Cardiovascular Risk in Type 2 Diabetes: What I Do an...Slides to Guide Reducing Cardiovascular Risk in Type 2 Diabetes: What I Do an...
Slides to Guide Reducing Cardiovascular Risk in Type 2 Diabetes: What I Do an...
 
Landmark trials in diabetes
Landmark trials in diabetesLandmark trials in diabetes
Landmark trials in diabetes
 
Intensive Glucose Control in Patients with Type 2 Diabetes — 15-Year Follow-up
Intensive Glucose Control in Patients  with Type 2 Diabetes — 15-Year Follow-upIntensive Glucose Control in Patients  with Type 2 Diabetes — 15-Year Follow-up
Intensive Glucose Control in Patients with Type 2 Diabetes — 15-Year Follow-up
 
DA 2020
DA 2020DA 2020
DA 2020
 
Diambassadors.com
Diambassadors.comDiambassadors.com
Diambassadors.com
 
Ueda2015 sanofi insulin therapy dr.khaled el-hadidy
Ueda2015 sanofi insulin therapy dr.khaled el-hadidyUeda2015 sanofi insulin therapy dr.khaled el-hadidy
Ueda2015 sanofi insulin therapy dr.khaled el-hadidy
 
RABBIT 2
RABBIT 2RABBIT 2
RABBIT 2
 
Diabetes nov2019 om alhamam (1)
Diabetes nov2019 om alhamam (1)Diabetes nov2019 om alhamam (1)
Diabetes nov2019 om alhamam (1)
 
Conway2019
Conway2019Conway2019
Conway2019
 
PCKS9 INHIBITORS
PCKS9 INHIBITORSPCKS9 INHIBITORS
PCKS9 INHIBITORS
 
Canagliflozin journal ppt
Canagliflozin journal pptCanagliflozin journal ppt
Canagliflozin journal ppt
 
Hope 3 trial acc 2016 (4) (1)
Hope 3 trial acc 2016 (4) (1)Hope 3 trial acc 2016 (4) (1)
Hope 3 trial acc 2016 (4) (1)
 
ueda2012 metabolic memory-d.mgahed
ueda2012 metabolic memory-d.mgahedueda2012 metabolic memory-d.mgahed
ueda2012 metabolic memory-d.mgahed
 
SPRINT BP Journal club
SPRINT BP Journal clubSPRINT BP Journal club
SPRINT BP Journal club
 
ESTUDIO ADVANCE: ESTUDIO DE DIABETES SOBRE USO DE GLICAZIDE
ESTUDIO ADVANCE: ESTUDIO DE DIABETES SOBRE USO DE GLICAZIDEESTUDIO ADVANCE: ESTUDIO DE DIABETES SOBRE USO DE GLICAZIDE
ESTUDIO ADVANCE: ESTUDIO DE DIABETES SOBRE USO DE GLICAZIDE
 

More from Isabella Nga Lai (20)

Vancomycin vs Metronidazole in C.Diff
Vancomycin vs Metronidazole in C.DiffVancomycin vs Metronidazole in C.Diff
Vancomycin vs Metronidazole in C.Diff
 
SONIC
SONICSONIC
SONIC
 
STOPAH
STOPAHSTOPAH
STOPAH
 
Fidaxomicin in cdiff
Fidaxomicin in cdiffFidaxomicin in cdiff
Fidaxomicin in cdiff
 
COLONPREV
COLONPREVCOLONPREV
COLONPREV
 
CYCLOPS
CYCLOPSCYCLOPS
CYCLOPS
 
ATN
ATNATN
ATN
 
ACT
ACTACT
ACT
 
SPARCL
SPARCLSPARCL
SPARCL
 
CORTICUS
CORTICUSCORTICUS
CORTICUS
 
Nice-Sugar
Nice-SugarNice-Sugar
Nice-Sugar
 
Jupiter Trial
Jupiter TrialJupiter Trial
Jupiter Trial
 
Ephesus
EphesusEphesus
Ephesus
 
Courage Trial
Courage TrialCourage Trial
Courage Trial
 
Affirm Trial
Affirm TrialAffirm Trial
Affirm Trial
 
SALT-E 2
SALT-E 2SALT-E 2
SALT-E 2
 
SALT-E 6
SALT-E 6SALT-E 6
SALT-E 6
 
SALT-E 5
SALT-E 5SALT-E 5
SALT-E 5
 
SALT-E 4
SALT-E 4SALT-E 4
SALT-E 4
 
SALT-E 3
SALT-E 3SALT-E 3
SALT-E 3
 

Recently uploaded

The basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptxThe basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptx
heathfieldcps1
 

Recently uploaded (20)

Unit-V; Pricing (Pharma Marketing Management).pptx
Unit-V; Pricing (Pharma Marketing Management).pptxUnit-V; Pricing (Pharma Marketing Management).pptx
Unit-V; Pricing (Pharma Marketing Management).pptx
 
Google Gemini An AI Revolution in Education.pptx
Google Gemini An AI Revolution in Education.pptxGoogle Gemini An AI Revolution in Education.pptx
Google Gemini An AI Revolution in Education.pptx
 
Accessible Digital Futures project (20/03/2024)
Accessible Digital Futures project (20/03/2024)Accessible Digital Futures project (20/03/2024)
Accessible Digital Futures project (20/03/2024)
 
Python Notes for mca i year students osmania university.docx
Python Notes for mca i year students osmania university.docxPython Notes for mca i year students osmania university.docx
Python Notes for mca i year students osmania university.docx
 
Towards a code of practice for AI in AT.pptx
Towards a code of practice for AI in AT.pptxTowards a code of practice for AI in AT.pptx
Towards a code of practice for AI in AT.pptx
 
SOC 101 Demonstration of Learning Presentation
SOC 101 Demonstration of Learning PresentationSOC 101 Demonstration of Learning Presentation
SOC 101 Demonstration of Learning Presentation
 
ICT role in 21st century education and it's challenges.
ICT role in 21st century education and it's challenges.ICT role in 21st century education and it's challenges.
ICT role in 21st century education and it's challenges.
 
Wellbeing inclusion and digital dystopias.pptx
Wellbeing inclusion and digital dystopias.pptxWellbeing inclusion and digital dystopias.pptx
Wellbeing inclusion and digital dystopias.pptx
 
FSB Advising Checklist - Orientation 2024
FSB Advising Checklist - Orientation 2024FSB Advising Checklist - Orientation 2024
FSB Advising Checklist - Orientation 2024
 
REMIFENTANIL: An Ultra short acting opioid.pptx
REMIFENTANIL: An Ultra short acting opioid.pptxREMIFENTANIL: An Ultra short acting opioid.pptx
REMIFENTANIL: An Ultra short acting opioid.pptx
 
TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...
TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...
TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...
 
2024-NATIONAL-LEARNING-CAMP-AND-OTHER.pptx
2024-NATIONAL-LEARNING-CAMP-AND-OTHER.pptx2024-NATIONAL-LEARNING-CAMP-AND-OTHER.pptx
2024-NATIONAL-LEARNING-CAMP-AND-OTHER.pptx
 
Micro-Scholarship, What it is, How can it help me.pdf
Micro-Scholarship, What it is, How can it help me.pdfMicro-Scholarship, What it is, How can it help me.pdf
Micro-Scholarship, What it is, How can it help me.pdf
 
The basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptxThe basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptx
 
80 ĐỀ THI THỬ TUYỂN SINH TIẾNG ANH VÀO 10 SỞ GD – ĐT THÀNH PHỐ HỒ CHÍ MINH NĂ...
80 ĐỀ THI THỬ TUYỂN SINH TIẾNG ANH VÀO 10 SỞ GD – ĐT THÀNH PHỐ HỒ CHÍ MINH NĂ...80 ĐỀ THI THỬ TUYỂN SINH TIẾNG ANH VÀO 10 SỞ GD – ĐT THÀNH PHỐ HỒ CHÍ MINH NĂ...
80 ĐỀ THI THỬ TUYỂN SINH TIẾNG ANH VÀO 10 SỞ GD – ĐT THÀNH PHỐ HỒ CHÍ MINH NĂ...
 
Single or Multiple melodic lines structure
Single or Multiple melodic lines structureSingle or Multiple melodic lines structure
Single or Multiple melodic lines structure
 
Making communications land - Are they received and understood as intended? we...
Making communications land - Are they received and understood as intended? we...Making communications land - Are they received and understood as intended? we...
Making communications land - Are they received and understood as intended? we...
 
How to Manage Global Discount in Odoo 17 POS
How to Manage Global Discount in Odoo 17 POSHow to Manage Global Discount in Odoo 17 POS
How to Manage Global Discount in Odoo 17 POS
 
Beyond_Borders_Understanding_Anime_and_Manga_Fandom_A_Comprehensive_Audience_...
Beyond_Borders_Understanding_Anime_and_Manga_Fandom_A_Comprehensive_Audience_...Beyond_Borders_Understanding_Anime_and_Manga_Fandom_A_Comprehensive_Audience_...
Beyond_Borders_Understanding_Anime_and_Manga_Fandom_A_Comprehensive_Audience_...
 
Fostering Friendships - Enhancing Social Bonds in the Classroom
Fostering Friendships - Enhancing Social Bonds  in the ClassroomFostering Friendships - Enhancing Social Bonds  in the Classroom
Fostering Friendships - Enhancing Social Bonds in the Classroom
 

ACCORD

  • 1. ACCORD The ACCORD Study Group. “Effects of intensive glucose lowering in Type 2 Diabetes” New England Journal of Medicine. 2008. 358(24):2545-59. SUMMARIZED BY MARIA MORKOS
  • 2. Action to Control Cardiovascular Risk in Diabetes (ACCORD) Summarized by: Maria Morkos, MD; Laxmi Suthar, MD
  • 3. BACKGROUND  Research has shown that in T2DM patients, a relationship exists between A1c levels and CV events  No previous study has investigated if intensive therapy to target normal A1c levels would decrease CV events in T2DM patients who had CV disease/risk factors
  • 4. CLINICAL QUESTION Would a therapeutic strategy targeting normal A1c levels (below 6% vs targeting A1c levels of 7.0-7.9%) reduce the rate of cardiovascular events in T2DM persons with established cardiovascular disease and/or additional cardiovascular risk factors?
  • 5. DESIGN  Analysis: chi square tests and two-sample t-tests  77 clinical centers across the US and Canada  N = 10,251  Group 1: received intensive therapy targeting an A1c of less than 6.0%  Group 2: received standard therapy targeting an A1c of 7.0 to 7.9%  Follow-up was 3.5 years (intensive therapy was discontinued after higher mortality was found in the intensive therapy group)  Primary outcomes:  first occurrence of nonfatal MI or stroke  or death from CV causes (MI, HF, stroke, CV cause of death after non-cardiovascular surgery)  Secondary outcome: death from any cause
  • 6. POPULATION Inclusion Criteria  T2DM and A1c of 7.5% or higher  ages 40-79 yo  CV disease or between 55-79 yo and had anatomical evidence of significant atherosclerosis, albuminuria, LVH, or at least 2 additional risk factors for CV disease (dyslipidemia, HTN, currently smoking, obesity) Exclusion Criteria  Frequent or recent serious hypoglycemic events  Unwillingness to do home glucose monitoring or inject insulin  BMI > 45  Serum Cr of > 1.5  Or other serious illness
  • 7. INTERVENTIONS  Group 1  received intensive therapy targeting A1c of less than 6.0%  attended monthly visits for the first 4 months then q2 months after that, with at least one interim phone call  Group 2 (Placebo Control)  received standard therapy targeting A1c of 7.0 to 7.9%  glycemic management visits q4 months  All patients received study formulary meds as well as glucose monitoring supplies  Any marketed anti-hyperglycemic therapy that was not provided by formulary could also be prescribed but was not provided by study investigators  Also received instructional materials and behavioral counseling regarding diabetes  Therapeutic regimens were individualized at investigators’ and patients’ discretion based on study-group assignment and response to therapy
  • 8. INTERVENTIONS (CONT’D)  Glucose lower drugs included: metformin, secretagogues, thiazolidinediones, an alpha glucosidase inhibitor, incretin, insulin  In addition…  4733 patients were randomly assigned to lower their BP by receiving either intensive therapy (SBP target <120) or standard therapy (SBP target <140)  5518 patients were randomly assigned, while on simvastatin, to either fenofibrate or placebo  At time of study publication, BP and lipid trials were still continuing
  • 9. RESULTS  At 1 year and after, throughout the follow-up period,  median A1c for intensive therapy group was 6.4%  median A1c for standard therapy group was 7.5%  The intensive therapy group had significantly higher rates of:  hypoglycemia (requiring assistance)  weight gain (>10 kg)  and fluid retention  The intensive therapy group had a lower rate of nonfatal MI BUT higher rate of death from CV causes; no significant difference in rates of nonfatal stroke  Rate of death from any cause was HIGHER in the intensive therapy group
  • 10. CRITICISMS/LIMITATIONS  Did not study the components of the intervention strategies used  Did not address an optimal rate to lower glucose levels  Glucose lowering strategies were adjusted for each patient in an open fashion based on their glycemic response to a drug/drug combination and the development of clinical sx such as hypoglycemia  No clear explanation for higher mortality found in intensive therapy group  ?Application to T2DM patients with A1c lower than 7.5% or T2DM patients w/o CV history or risk factors  Benefits from intensive glucose lowering therapy may need more than 3.5 years to emerge
  • 11. BOTTOM LINE Therapeutic targeting of A1c levels below 6.0% INCREASED the rate of death from any cause after a mean of 3.5 years, as compared with a strategy targeting levels of 7.0-7.9% In patients with a median A1c 8.1% and previous CV events/multiple CV risk factors
  • 12. DISCUSSION QUESTIONS  What are two important inclusion criteria for the diabetic population this trial targeted?  What were the target A1c levels of the two different therapy groups?  What was the outcome discovered after ~3 years of the trial?
  • 13. DISCUSSION ANSWERS  What are two important facts about the patient population this trial targeted?  ANSWER: Had A1c greater than 7.5% and had to have either a CV event in past or several CV risk factors  What were the target A1c levels of the two different therapy groups?  ANSWER: intensive therapy group target was A1c < 6.0%; standard therapy group target was A1c 7.0-7.9%  What was the outcome discovered after ~3 years of the trial?  ANSWER: intensive therapy to target lower A1c levels (<6.0%) increased mortality and did not significantly reduce major cardiovascular events
  • 14. BOARD-LIKE QUESTION 43 yo M is evaluated during a follow-up visit for management of T1DM. Pt has had multiple complications including ESRD, gastroparesis, frequent hypoglycemia with hypoglycemic unawareness, painful neuropathy, and proliferative retinopathy. He uses an insulin pump and checks fingerstick glucoses several times during the day, which range from 65 to 250. Most recent A1c is 7.5% (Adapted from MKSAP 17) QUESTION Which of the following is the most appropriate next step in the management of this patient? A. Alter insulin pump settings to attain an A1c of less than 7.0% B. Alter insulin pump settings to decrease the insulin doses C. Discontinue the insulin pump, start subQ insulin injections D. Start gabapentin for treatment of painful peripheral neuropathy
  • 15. BOARD-LIKE QUESTION Educational Objective: Liberalize glycemic targets in a patient with multiple diabetic complications and advanced microvascular disease Key Point: - Frequent hypoglycemia/hypoglycemic unawareness increases the risk of morbidity and mortality - A less stringent A1c goal (such as 8%, per the ADA) is appropriate for persons with DM with a decreased life expectancy, history of severe hypoglycemia, multiple comorbidities, or advanced micro/macrovascular disease QUESTION Which of the following is the most appropriate next step in the management of this patient? A. Alter insulin pump settings to attain an A1c of less than 7.0% B. Alter insulin pump settings to decrease the insulin doses C. Discontinue the insulin pump, start subQ insulin injections D. Start gabapentin for treatment of painful peripheral neuropathy
  • 16. REFERENCES  Effects of intensive glucose lowering in Type 2 Diabetes (2008). New England Journal of Medicine, 358:2545.-2559. doi 10.1056/NEJMoa0802743