Recent changes to MOC and criticism of ABIM, where does nephrology stand. Bold move by ASN to interview with founder of the new organization National Board of Physicians and Surgeons(NBPAS).
I think starting this discussion now is so critical. Hats off to Tod Ibrahim and ASN to take this initiative as we need to redefine that is reasonably priced and truly looks at clinical work that we do.
http://asn-online.org/media/podcast.aspx?p=kidneynews&e=2015_06_25_Teirstein.mp3
Saturday, June 27, 2015
Tuesday, June 23, 2015
IN the NEWS: GN Types and ESRD
How do different GN
types do on ESRD? A recent USRDS analysis looked at this very question.
1. Over
84,000 patients were found to have GN that were on ESRD In the time period reviewed
2. Interestingly
IgA nephropathy had the fewest other comorbidities and the lowest use of
hemodialysis
3. Crude
mortality was also lowest in IgA nephropathy patients
4. Highest
mortality was in Lupus nephritis and diabetic nephropathy patients when
compared to IgAN
5. Patients
with ADPKD had a relatively favorable comorbidity and laboratory profile, comparable
with that in IgAN.
6. Overall,
LN patients did the worst of all GNs.
7. Cardiovascular
disease accounted for the highest proportion of deaths within all GN subtypes,
ranging from 34.2% in vasculitis to 44.6% in FSGS.
8. The
highest proportion of infection-related deaths was observed in LN
9. There
were marked survival discrepancies that persisted even after adjustment for
socio demographic and clinical factors.
10. Some
GN subtypes (e.g., IgAN) conferred a particularly favorable prognosis, superior
to that in ADPKD as stated above but, LN displayed shortened survival, similar
to in patients with ESRD caused by diabetes.
These are some very
important findings of the study. Categorizing GNs as on major cause of ESRD
might be not helping us figure out the long term outcomes. As expected IgA and
ADPKD have better survivals and some of the autoimmune and immunosuppressive prone
GNs had worse outcomes.
Labels:
CKD and ESRD,
glomerular diseases,
In The News
Saturday, June 6, 2015
OncoNephrology Conference 2015
We are conducting a one day symposium on OncoNephrology: Cancer, chemotherapy and the Kidney at Hofstra NSLIJ School of Medicine on Sept 26th, 2015 from 7:30AM to 4PM
The conference will highlight and review the latest happenings in OncoNephrology
Talks and Speakers highlighted;
AKI in Cancer Patients; Joseph Bonventre, Harvard Medical School
Chemotherapy Toxicities: Mark Perazella, Yale University
Targeted Therapy and the Kidney: Kenar Jhaveri, Hofstra University
Hypercalcemia of Malignancy: Naveed Masani, Winthrop University
Anemia, CKD, ESKD and cancer: Steven Fishbane, Hofstra University
Renal Cancer, an update: Thomas Bradley, Hofstra University, NSLIJ Cancer Institute
Paraneoplastic GN; Hitesh H Shah, Hofstra University
TMA: Bradley Dixon, Cincinnati Children Hospital
Post Kidney Transplant Cancers: Vinay Nair, Mt Sinai Medical Center
Paraproteinemias, an update: Gerald Appel, Columbia University Medical Center
Cases with the Onconephropathologist: Glen Markowitz, Columbia Medical Center
Course directors: Kenar Jhaveri, Steven Fishbane and Thomas Bradley( Division of Nephrology and Hematology/Oncology at Hofstra NSLIJ School of Medicine)
Planning committee: Kenar Jhaveri, Steven Fishbane and Thomas Bradley, Hitesh H Shah, Pravin Singhal, Jyotsana Thakkar and Rimda Wanchoo( all from Division of Nephrology, Hofstra NSLIJ School of Medicine)
To Register: go here
Full brochure coming soon.
This conference is endorsed by




The conference will highlight and review the latest happenings in OncoNephrology
Talks and Speakers highlighted;
AKI in Cancer Patients; Joseph Bonventre, Harvard Medical School
Chemotherapy Toxicities: Mark Perazella, Yale University
Targeted Therapy and the Kidney: Kenar Jhaveri, Hofstra University
Hypercalcemia of Malignancy: Naveed Masani, Winthrop University
Anemia, CKD, ESKD and cancer: Steven Fishbane, Hofstra University
Renal Cancer, an update: Thomas Bradley, Hofstra University, NSLIJ Cancer Institute
Paraneoplastic GN; Hitesh H Shah, Hofstra University
TMA: Bradley Dixon, Cincinnati Children Hospital
Post Kidney Transplant Cancers: Vinay Nair, Mt Sinai Medical Center
Paraproteinemias, an update: Gerald Appel, Columbia University Medical Center
Cases with the Onconephropathologist: Glen Markowitz, Columbia Medical Center
Course directors: Kenar Jhaveri, Steven Fishbane and Thomas Bradley( Division of Nephrology and Hematology/Oncology at Hofstra NSLIJ School of Medicine)
Planning committee: Kenar Jhaveri, Steven Fishbane and Thomas Bradley, Hitesh H Shah, Pravin Singhal, Jyotsana Thakkar and Rimda Wanchoo( all from Division of Nephrology, Hofstra NSLIJ School of Medicine)
To Register: go here
Full brochure coming soon.
This conference is endorsed by
Sunday, May 31, 2015
IN THE NEWS: Remote ischemic preconditioning and prevention of AKI post CABG

Remote ischemic preconditioning(RIPC)
has been used as a protective method
from ischemic damage to distant organs. Application
of one or more brief cycles of nonlethal ischemia/reperfusion to an organ or tissue
may protect a remote organ or tissue from a sustained episode of lethal
ischemia/reperfusion.
In a recent study presented at
Europe and published in JAMA, Zarbock et al examine the effects of RIPC on
the rate and severity of AKI in patients undergoing cardiac surgery. In a
multicenter trial, 240 patients at high risk for AKI were randomized to receive either RIPC or sham control after induction of anesthesia.
The amazing
results showed that AKI was significantly reduced with RIPC (45/120; 37.5%)
compared with control (63/120; 52.5%), with an absolute risk reduction (ARR) of
15%. Fewer patients received RRT after RIPC (7 [5.8%] vs 19 control [15.8%];
ARR, 10%) and RIPC reduced intensive care unit stay (3 vs 4 days). RIPC had no
significant effect on myocardial infarction, stroke, or mortality.
Can we
start using this in clinical practice? It is innovative, inexpensive and easily
possible. But long terms risks and harms
are not known. Clearly, there is significant risk of AKI post CABG and this might be the only
preventive measure that we have that has come close to showing any
benefit.
As suggested by the editorial in JAMA, before RIPC is adopted
for clinical use, the potential risks and adverse effects must be considered
carefully.
image source: circres.ahajournals.org
Thursday, May 28, 2015
ASN Fellows Survey on Workforce 2015
Nephrology Workforce Annual Fellows report in 2015 is being collected by ASN via a survey.
This survey, being performed by colleagues at Geoorge Washington University, will be very useful to understand our workforce related concerns. A prior survey done in 2014 had some alarming results.
See link below at ASN website.
http://asn-online.org/education/training/workforce/home.aspx
The Workforce committee of ASN has spent the last 5 years or more attempting to draw conclusions about fellowship trends and workforce needs from fragmented information. This is one of our few opportunities to gather good data and have it analyzed by those with expertise in healthcare workforce studies.
I think the fellows in the USA should take this opportunity to help out the field of Nephrology. Youshould try to must complete the survey you received from ASN.
This survey, being performed by colleagues at Geoorge Washington University, will be very useful to understand our workforce related concerns. A prior survey done in 2014 had some alarming results.
See link below at ASN website.
http://asn-online.org/education/training/workforce/home.aspx
The Workforce committee of ASN has spent the last 5 years or more attempting to draw conclusions about fellowship trends and workforce needs from fragmented information. This is one of our few opportunities to gather good data and have it analyzed by those with expertise in healthcare workforce studies.
I think the fellows in the USA should take this opportunity to help out the field of Nephrology. You
Labels:
asn media center,
education,
workforce
Tuesday, May 19, 2015
Topic Discussion: Non uremic causes of calciphylaxis
Calciphylaxis, or
calcific uremic arteriolopathy(CUA), is a well-described entity in end-stage
kidney disease and renal transplant patients; however, little systematic
information is available on calciphylaxis from nonuremic causes.
A review I found in
CJASN from 2008 discusses non renal causes of CUA.
Besides renal
disease, the non uremic( CKD and ESRD) causes are: the top 4 being the most
cases of. The remaining were just 1-2 case reports. Most of these patients listed below had
normal renal function, over 50% had normal calcium and >60% had normal
phosphorus levels and 50% had low or normal pth levels. One most keep these
causes in mind when ESRD or CKD does not explain the cause of CUA.
Primary hyperparathyroidism
Malignancy( Classically breast, melanoma, gall bladder, myeloma)
Alcoholic liver disease
Connective tissue diseases
Chemo induced protein C and S deficiency
Crohn’s disease
Vitamin D deficiency
POEMS syndrome
Diabetes
Malignancy( Classically breast, melanoma, gall bladder, myeloma)
Alcoholic liver disease
Connective tissue diseases
Chemo induced protein C and S deficiency
Crohn’s disease
Vitamin D deficiency
POEMS syndrome
Diabetes
Labels:
calciphylaxis,
CKD and ESRD,
topic discussions
Monday, May 18, 2015
NK cell leukemia and lymphomas and renal disease
NK cell
neoplasms have a wide range of clinical, morphologic, and immunophenotypic
characteristics. Aggressive NK cell leukemia usually
affects young patients in their 20-30s with equal sex incidence and shows a
rapidly progressive clinical course. Often they don’t respond well to chemotherapy
and prognosis is poor.
Kidney
involvement in these cancers is rare but here is what I found?
One case
report of a collapsing FSGS published in AJKD in 2011. Initially, in this
case, the first biopsy was read as FSGS NOS and then a repeat one had
collapsing glomerulopathy.
Another recent case
series describes cases of renal diseases seen with all types of non-Hodgkin’s
lymphoma. They describe 20 cases. T/NK cell lymphoma was
in 4 cases. 2 of the 4 cases had crescentic GN, 1 had minimal change disease
and 1 had infiltrative disease.
A very early description
of minimal change disease has been described in a case report in 1980s of a
large granular cell lymphoma.
So in summary, NK cell neoplasms likely are
related to cause some glomerular involvement-likely podocytopathies such as minimal
change to FSGS. Cases of crescentic GN have also been described.
Labels:
glomerular diseases,
NK cells,
onco nephrology
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