Dr.
Yitzchak Goldstein (whose formal name is actually Dr. Doctor Y. Goldstein – but
more on this below!) is putting his love for science and technology into action
at Montefiore Medical Center.
When
he’s not busy on his Cytology rotation, the third-year pathology resident
spends his time analyzing data mined from thousands of electronic records to
determine whether certain laboratory tests can accurately predict a patient’s future
risk of developing a life-threatening blood clot.
Using
Clinical Looking Glass (CLG), a
proprietary analytics software program developed by researchers and clinicians
at Montefiore Medical Center, Dr. Goldstein is able to collect clinical and
laboratory data on hospital patients to determine who has been tested for
certain antibodies, which tests came back positive, which came back negative,
and which patients developed a clot.
In
the past, this type of analysis required laborious and time consuming reviews
of patient medical records – not to mention the not infrequent difficulties of
deciphering handwritten physicians’ notes. However, using CLG, thousands
of patients who had a lab test performed can be followed over time with
computer-assistance to see if - and when - they develop a clot.
“If
we can identify those patients who are at high risk of developing a clot, we
can say it’s someone for whom clinicians should consider medicating with
anti-coagulants,” said Dr. Goldstein, 30, who is
assisting Dr. Jacob Rand, a hematologist, and professor in the department of
pathology at Einstein and director of the medical center’s Hematology
Laboratories.
 Jacob Rand, MDDr. Rand’s research laboratory
focuses on the investigation of the effects of antiphospholipid (aPL)
antibodies on an anticoagulant protein, annexin A5 (previously known as annexin
V). The antiphospholipid (aPL) syndrome is an enigmatic autoimmune disorder
that is characterized by thrombosis and/or recurrent spontaneous pregnancy
losses that occur in patients who have evidence for antibodies against
phospholipid-binding proteins. Deep vein thrombosis (DVT) and pulmonary embolism (PE) – clots in the legs and lungs
– are often under-diagnosed and serious, but preventable medical
conditions.
The CDC estimates between 300,000 to 600,000 people are affected by blood clots,
and every year between 60,000 and 100,000 die.
But
predicting who is going to develop a clot and what laboratory tests can be used
to determine the likelihood is no easy task.
Blood tests for APS look for at
least one of three antibodies - anticardiolipin, beta-2 glycoprotein I and lupus anticoagulant, and the
antibodies must appear in the blood at least twice to confirm the
diagnosis.
“Right now for a patient who has the antibodies, we wait to
see if they develop a second clot. It’s difficult to tease out who should be on
an anti-coagulant because there are risks associated with prescribing them,
including bleeding and strokes,” Dr. Goldstein said. “If you have a patient that we have identified as being at high
risk, you can say it’s someone for whom a ‘blood thinner’ should be
considered.”
To
create a baseline, he collected records of all Accountable Care Organization (ACO) patients and followed them using CLG to see who developed a clot. He then
compared the risk in those patients to patients who had tested positive for
each of the antiphospholipid antibodies.
The
results were striking.
One
test, the lupus anticoagulant, showed a markedly elevated probability of
developing a clot, whereas the other antibody tests seemed to show some risk
but to a lesser degree than the lupus anticoagulant over the baseline.
“If
we’re talking about which tests to start thinking about for a patient; if lupus
anticoagulant comes back positive it’s already considered a high risk, and our
data strengthens that point,” Dr. Goldstein said.
“We
see that each of the antibodies has an increased risk of thrombosis over the
baseline, but that not all antibodies are created equal in their ability to
predict and prognosticate the development of a clot.”
By
developing a scoring system, pathologists can see who is at high risk and treat
patients accordingly.
.JPG) Dr. Goldstein presenting his research at The American Society of Hematology's (ASH) Annual
Meeting, in New Orleans, LA.The
CLG program was created in 2002 by Montefiore clinicians and administrators
driven to find information that could possibly control the rampant spread of
tuberculosis and HIV among 15,000 inmates at Riker’s Island.
It has since been used in many programs at Montefiore
and outside the medical center.
For example, CLG has helped identify the 58% of diabetics who were
not being successfully controlled, leading to targeted outreach activities
which reduced the percentage of uncontrolled diabetics by over one-third.
So
far, Dr. Goldstein has amassed data from over 11,000 patients dating back to
about 1996. He says the
information can help better target at-risk patients for treatment.
He recently presented his findings regarding the antiphospholipid
antibodies using CLG at The American Society of Hematology's (ASH) Annual
Meeting, in New Orleans.
A native New Yorker and Einstein
graduate, his training at Montefiore as a pathology resident has brought his
life full-circle. After all, he
was born in Weiler hospital, where his mother worked as an OR nurse for 33
years.
His birth name -“Doctor Goldstein” - often lends itself to a unique conversation starter on
first-time introductions.
Known
as Yitz, he was named after his grandfather, a PhD chemistry professor, also
named Yitzchak, who everyone referred to as “Doctor" and passed away a few weeks before Yitz was
born.
 Dr. Doctor Goldstein's Montefiore ID badgeThe
future Doctor Goldstein, MD, grew up in Hillcrest, Queens
and went to Yeshiva’s High School, the Marsha Stern Talmudical Academy. He went on to study in Israel for two
years before returning to Queens to attend Lander College, where he was the president of
the biological society and met his future wife, Mati. He completed his medical training at the Albert Einstein
College of Medicine, and went on to his pathology residency at Montefiore. Dr. Goldstein lives in Riverdale with
his wife and two children.
“I’m
a guy who just grew up loving the sciences, who ended up in the sciences,” he
said, noting that he is passionate about passing his enthusiasm on to his 5-year-old
daughter.
“I
get such great enjoyment out of explaining to her how a rainbow is made or how
salt melts ice,” he added.
On
campus Dr. Goldstein takes part in Einstein’s career speed dating – talking to
medical students about the diverse nature of pathology as career.
In
his free, time he enjoys digitally editing photos for friends and family, and
creating paper cut out art, which was displayed last year at Einstein's
Ad-Libitum yearly Art Show.
A
self-described science and computer geek, Dr. Goldstein is particularly
interested in the technologies of molecular genetic pathology and the myriad
ways with which current technologies manipulate DNA.
“One
day soon we’ll be able to take all of this genomic information and distill it
to the point where we can tell a patient precisely what they are risk for” he
said.
“The
ways in which we will be able to precisely personalize medicine, utilizing all
of the advanced technologies at our disposal, simply blows my mind every day.”
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