Aisha Shaikh Profile picture
Sep 30, 2020 23 tweets 12 min read Read on X
💥KDIGO 2020 Clinical Practice Guideline for Diabetes Management in CKD
Tweetorial

☄️Comprehensive Care in DM & CKD

☄️Glycemic Monitoring & Targets

☄️Lifestyle Interventions

☄️Anti-glycemic Rx

👉🏽 tinyurl.com/yyth59kn
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@goKDIGO @Kidney_Int
#KDIGO
💥Before reviewing the guidelines, note the difference between the:

⚡️Recommendations
⚡️Practice Points

💥Recommendations are based on strong evidence whereas for the Practice Points the evidence is insufficient or inconclusive👇🏽

2/
💥Comprehensive Care is needed for pts. with DM & CKD to ⬇️ risk of
CV disease & Kidney Disease progression👇🏽

✅ Glycemic Control
✅ BP Control
✅ Lipid Rx
✅ Nutrition
✅ Exercise
✅ Smoking Cessation

🌟RAS Blockade & SGLT2i👇🏽

🌟Anti-platelet Rx👇🏽

3/
💥 RAS blockade w/ ACEi or ARB is recommended in pts. w/ DM, HTN & Albuminuria & the dose should be titrated to the highest approved dose tolerated by the pt.

⚡️Monitoring of serum creatinine & K during Rx w/ RAS blockers👇🏽
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💥RAS blockade may be considered in pts. w/ DM, Albuminuria & no HTN

⚡️Benefits of RAS blockade in this group are less studied but it may be beneficial due to the strong correlation b/w the severity of albuminuria & ESKD in DM
👉🏽 nature.com/articles/hr200…

5/
💥RAS blockade in T1DM patients with no Albuminuria & no HTN is generally not considered beneficial

⚡️In T1DM patients, RAS blockade did not slow progression of CKD or ⬇️ the incidence of albuminuria over 5 years👇🏽
pubmed.ncbi.nlm.nih.gov/19571282/

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💥RAS Blockade in T2DM w/ no Albuminuria & no HTN is gen. not considered beneficial

⚡️One study showed ⬇️ in incident albuminuria but ⬆️CV events👇🏽
⚡️Another review showed benefit in normoalbuminuric pts. on albuminuria progression but most pts. had HTN👇🏽
7/
💥Here is a list of the different formulations of ACEi & ARBs:

⚡️Recommended starting dose
⚡️Recommended max. daily dose
⚡️Dose adjustment in CKD
⚡️Removal during hemodialysis

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💥Glycemic Monitoring & Target

⚡️Monitor HbA1c 2x/year or more often if BG control is poor

⚡️Target AIC: <6.5% to <8.0%

⚡️Accuracy of HbA1c is ⬇️ in CKD esp. in ESKD👇🏽

⚡️Continuous Glucose Monitoring can be used when A1c is not reliable👇🏽

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💥Lifestyle Interventions

❇️ Protein intake:
⚡️0.8 g/kg/day in pts. w/ DM & Non-dialysis CKD
⚡️1.0-1.2 g/kg/day for pts. on dialysis👇🏽

❇️ Sodium intake <2 g/day (<5 g NaCl/day)👇🏽

❇️ Physical Activity of moderate intensity for at least 150 min./wk

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💥 Anti-glycemic Rx in Pts. w/ T2DM & CKD

⚡️Lifestyle therapy:
☄️Exercise, Nutrition & Wt. loss

⚡️1st-line Drug Rx:
☄️Metformin + SGLT2i

⚡️Additional Drug Rx is guided by patient preference, comorbidities, eGFR & cost
☄️GLP-1 RA is preferred👇🏽

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💥T2DM + CKD pts. w/ eGFR of
> or = 30 ml/min benefit from both Metformin & SGLT2i

⚡️Metformin: good anti-glycemic effect but modest impact on long term DM complications

⚡️SGLT2i: weak anti-glycemic effect but large effect on ⬇️ CKD progression & CVD

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💥DAPA-CKD Trial was published on 9/24/20
⚡️KDIGO guidelines were written prior to DAPA-CKD publication & will be updated to reflect the eGFR cutoff

⚡️Dapagliflozin showed renal benefit in CKD w/ & w/o T2DM w/ eGFR of 25-75 ml/min & ACR 200 mg/g or > 👇🏽

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💥In drug naive pts. (those not on Metformin or SGLT2i), which drug should be started first?

☄️No high-quality data comparing initiation of Metformin vs. initiation of SGLT2i

☄️In most large trials, SGLT2i was added to Metformin

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💥In drug naive pts (not on Metformin or SGLT2i):

1. Start Metformin & add SGLT2i

2. It may be practical to start low dose of both agents to manage glycemia & get organ protection benefits of SGLT2i👇🏽

⚡️Metformin & SGLT2i dose adjustment in CKD👇🏽
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💥If a pt. w/ T2DM + CKD w/ eGFR of >30ml/min is achieving glycemic target w/ Metformin alone:

⚡️Then try to lower the Metformin dose & add SGLT2i

⚡️Addition of SGLT2i is unlikely to cause hypoglycemia but yet offer the Kidney & CV benefits

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💥Based on current evidence:

⚡️Metformin must be stopped if eGFR drops to <30 ml/min

⚡️If Canagliflozin is initiated at eGFR of >30 ml/min, then it can be continued till the start of kidney replacement therapy (as was done in the CREDENCE Trial)

17/
💥If glycemic target is NOT met w/ Metformin + SGLT2i then GLP-1 RA is preferred because of it’s demonstrated CV benefits & possible kidney benefits👇🏽

⚡️Consider Pt. Factors when selecting a glucose lowering drug to add to Metformin & SGLT2i👇🏽

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💥Most GLP-1 RA are injectable drugs except Semaglutide

⚡️Side effects include GI symptoms
⚡️Contraindicated in pts. w/ h/o medullary thyroid ca, MEN-2, acute pancreatitis
⚡️GLP-1 RA should NOT be used w/ DPP-4 Inh.
⚡️GLP-1 RA dose adjustment in CKD👇🏽

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💥Large Trial Data - Summary

⚡️Overview of the large, placebo-controlled trials assessing the benefits of SGLT2i, GLP-1 RA & DPP-4 inhibitors👇🏽

⚡️CV & Kidney Outcome Trials for SGLT2i👇🏽

⚡️CV & Kidney Outcome Trials for GLP-1 RA👇🏽

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💥Summary of DM management in CKD

⚡️Comprehensive Care
⚡️Lifestyle Interventions
⚡️RAS Blockade
⚡️T2DM: Initiate metformin & SGLT2i if eGFR criteria met
⚡️T2DM: If BG target not reached w/ Metformin + SGLT2i then GLP-1 RA is preferred

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💥KDIGO Research Recommendations👇🏽

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💥Here is the link to the complete KDIGO 2020 Guideline for Diabetes Management in Chronic Kidney Disease
👉🏽 tinyurl.com/yyth59kn

💥Link to the Executive Summary of the 2020 KDIGO Diabetes Management in CKD Guideline
👉🏽 tinyurl.com/yydxghoy

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More from @aishaikh

May 2, 2023
An interesting case of new onset HTN and hypokalemia in a patient with leiomyosarcoma

Serum K 2.9
BP 150/90
No accompanying acidosis or alkalosis👇🏽
1/

#onconephrology Image
Step 1: Is the hypokalemia due to renal K losses or extra-renal K losses?

24 hour urine K was 46 mEq/L so renal K losses were contributing to hypokalemia

Serum magnesium was normal

Patient was not on diuretics👇🏽
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In the setting of new onset hypokalemia and new onset HTN, there was high suspicion for mineralocorticoid excess or AME

So, plasma renin activity (PRA) and plasma aldosterone were checked

‼️Both PRA and aldosterone were elevated👇🏽
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Nov 4, 2022
The most anticipated nephrology trial of the year has been published!
“Empagliflozin in Patients with Chronic Kidney Disease” #Kidneywk
@NEJMnejm.org/doi/full/10.10…
EMPA-KIDNEY trial is a randomized, parallel-group, double-blind, placebo-controlled trial designed to assess the effect of empagliflozin on progression of kidney disease & CV disease, & to examine safety profile of the drug in a wide range of pts. w/ CKD
The trial included patients without diabetes, patients with an eGFR of less than 30 ml per minute per 1.73 m2, and patients with low levels of proteinuria
Read 18 tweets
Jul 21, 2022
📌 Tweetorial on “IgA Nephropathy: Approach to treatment” based on @goKDIGO webinar by Dr. Richard Lafayette

🔸First step in management of IgAN: Determine the risk of disease progression based on GFR, proteinuria, BP & kidney biopsy findings👇🏽
1/ Image
📌 Approach to treatment of IgAN based on @goKDIGO guidelines👇🏽

🔸This Rx algorithm is NOT applicable to IgA deposition with minimal change disease, IgAN with AKI, IgAN with RPGN, IgA vasculitis, IgA-dominant post-infections GN & secondary forms of IgAN👇🏽
2/ Image
📌 IgAN: All patients should receive supportive care:
🔸 Optimal BP management
🔸 Maximally tolerated ACEi/ARB
🔸 Lifestyle modification
🔸 Reduction of cardiovascular
risk👇🏽
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Jun 28, 2022
📌 Tweetorial on Diagnosis & Pathogenesis of IgA Nephropathy (IgAN) based on @goKDIGO webinar by @AgnesFogo & Dr. Jurgen Floege
#IgAN
🔸Interesting fact: IgAN is not a new disease
First known case of IgAN was found in Prince Joseph of Austria (1776-1847)
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📌 IgAN is characterized by:

🔸Mesangial immune-complex deposits which sometimes can extend to the capillary loops & sub-endothelial locations

🔸 Dominant IgA deposits compared to the other immunoglobulins
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📌 IgA deposits in IgAN are typically polyclonal & lambda is more prominent than kappa

🔸This is thought to represent the mucosal IgA
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Dec 21, 2021
Dr. Carlos Flombaum from @MSK_Neph gave a holiday lecture full of historic pearls. We are so lucky to have Dr. Flombaum in our division!
Did you know how Cisplatin was ‘accidentally’ discovered?👇🏽
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Dec 2, 2021
Workup for detection of Monoclonal Immunoglobulin (MIg) in patients with Monoclonal Gammopathy of Renal Significance (MGRS)

(Talk by Dr. Frank Bridoux at the Kidney Week)
#Onconephrology #MGRS
Workup for detection of Monoclonal Immunoglobulin

1. Find the circulating monoclonal Ig:

-SPEP & UPEP to quantify the Monoclonal (M) spike

-Serum & Urine Immunofixation to identify the monoclonal Ig & also to monitor response to Rx
2. Serum Free Light Chain Assay to identify free light chains & to monitor hematological response to Rx in Light Chain-associated kidney disorders

There are 2 different LC assays: Binding site & N-Latex assay
-Use same assay to follow LC levels Image
Read 9 tweets

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