If I have ever made any valuable discoveries, it has been owing more to patient observation than to any other reason. -Isaac Newton (1642-1727)
Happy Holidays!
-Ben
Thursday, December 25, 2014
Thursday, December 18, 2014
Benefits, Harms, and Cost-Effectiveness of Supplemental Ultrasonography Screening for Women With Dense Breasts
Congratulations to UVM Assistant Professor of Surgery Brian Sprague, PhD on publication of his latest work on the importance of mammographic breast density in Annals of Internal Medicine.
Sprague BL, Stout NK, Schechter C, van Ravesteyn NT, Cevik M, Alagoz O, et al. Benefits, Harms, and Cost-Effectiveness of Supplemental Ultrasonography Screening for Women With Dense Breasts. Ann Intern Med. [Epub ahead of print 9 December 2014] doi:10.7326/M14-0692
Background: Many states have laws requiring mammography facilities to tell women with dense breasts and a negative screening mammography result to discuss supplemental screening tests with their providers. The most readily available supplemental screening method is ultrasonography, but little is known about its effectiveness.
Objective: To evaluate the benefits, harms, and cost-effectiveness of supplemental ultrasonography screening for women with dense breasts.
Design: Comparative modeling with 3 validated simulation models.
Data Sources: Surveillance, Epidemiology, and End Results Program; Breast Cancer Surveillance Consortium; and medical literature.
Target Population: Contemporary cohort of women eligible for routine screening.
Time Horizon: Lifetime.
Perspective: Payer.
Intervention: Supplemental ultrasonography screening for women with dense breasts after a negative screening mammography result.
Outcome Measures: Breast cancer deaths averted, quality-adjusted life-years (QALYs) gained, biopsies recommended after a false-positive ultrasonography result, and costs.
Results of Base-Case Analysis: Supplemental ultrasonography screening after a negative mammography result for women aged 50 to 74 years with heterogeneously or extremely dense breasts averted 0.36 additional breast cancer deaths (range across models, 0.14 to 0.75 deaths), gained 1.7 QALYs (range, 0.9 to 4.7 QALYs), and resulted in 354 biopsy recommendations after a false-positive ultrasonography result (range, 345 to 421 recommendations) per 1000 women with dense breasts compared with biennial screening by mammography alone. The cost-effectiveness ratio was $325 000 per QALY gained (range, $112 000 to $766 000 per QALY gained). Supplemental ultrasonography screening for only women with extremely dense breasts cost $246 000 per QALY gained (range, $74 000 to $535 000 per QALY gained).
Results of Sensitivity Analysis: The conclusions were not sensitive to ultrasonography performance characteristics, screening frequency, or starting age.
Limitation: Provider costs for coordinating supplemental ultrasonography were not considered.
Conclusion: Supplemental ultrasonography screening for women with dense breasts would substantially increase costs while producing relatively small benefits.
Full report here.
UVM Bog report here.
Sprague BL, Stout NK, Schechter C, van Ravesteyn NT, Cevik M, Alagoz O, et al. Benefits, Harms, and Cost-Effectiveness of Supplemental Ultrasonography Screening for Women With Dense Breasts. Ann Intern Med. [Epub ahead of print 9 December 2014] doi:10.7326/M14-0692
Background: Many states have laws requiring mammography facilities to tell women with dense breasts and a negative screening mammography result to discuss supplemental screening tests with their providers. The most readily available supplemental screening method is ultrasonography, but little is known about its effectiveness.
Objective: To evaluate the benefits, harms, and cost-effectiveness of supplemental ultrasonography screening for women with dense breasts.
Design: Comparative modeling with 3 validated simulation models.
Data Sources: Surveillance, Epidemiology, and End Results Program; Breast Cancer Surveillance Consortium; and medical literature.
Target Population: Contemporary cohort of women eligible for routine screening.
Time Horizon: Lifetime.
Perspective: Payer.
Intervention: Supplemental ultrasonography screening for women with dense breasts after a negative screening mammography result.
Outcome Measures: Breast cancer deaths averted, quality-adjusted life-years (QALYs) gained, biopsies recommended after a false-positive ultrasonography result, and costs.
Results of Base-Case Analysis: Supplemental ultrasonography screening after a negative mammography result for women aged 50 to 74 years with heterogeneously or extremely dense breasts averted 0.36 additional breast cancer deaths (range across models, 0.14 to 0.75 deaths), gained 1.7 QALYs (range, 0.9 to 4.7 QALYs), and resulted in 354 biopsy recommendations after a false-positive ultrasonography result (range, 345 to 421 recommendations) per 1000 women with dense breasts compared with biennial screening by mammography alone. The cost-effectiveness ratio was $325 000 per QALY gained (range, $112 000 to $766 000 per QALY gained). Supplemental ultrasonography screening for only women with extremely dense breasts cost $246 000 per QALY gained (range, $74 000 to $535 000 per QALY gained).
Results of Sensitivity Analysis: The conclusions were not sensitive to ultrasonography performance characteristics, screening frequency, or starting age.
Limitation: Provider costs for coordinating supplemental ultrasonography were not considered.
Conclusion: Supplemental ultrasonography screening for women with dense breasts would substantially increase costs while producing relatively small benefits.
Full report here.
UVM Bog report here.
Tuesday, December 16, 2014
Peter Durda's abstract accepted for poster presentation
A recent abstract submitted by Peter Durda to the American Heart Association has been accepted for a poster presentation at the EPI/Lifestyle 2015 Scientific Sessions, scheduled March 3 - 6, 2015 at the Baltimore Marriott in Baltimore, Maryland. The presentation title is Circulating Soluble CD163 and Risk of Cardiovascular Disease and All-Cause Mortality in Older Persons: The Cardiovascular Heart Study (CHS).
Congratulations Peter!
Congratulations Peter!
Clinical Research Oriented Workshop (CROW) Meeting: Dec 11, 2014
Present: Marianne Burke, Nancy Gell, Kairn Kelley, Connie
van Eeghen
Start Up:
Watch out for undelivered emails (Nancy’s current problem) and new
levels of unwanted spam (Connie’s)
1.
Discussion Karen’s
Results section of her Dichotic Listening Test-Retest Draft
a. To
be submitted to a journal for speech/language, one of 3 requirements for
Kairn’s degree
b. This
draft focused on the differences among 3 tests; the next will look at the clinical
implications of the change in scores – how the difference might affect
diagnosis.
c. Results
reporting includes group and individual test reliability, which may begin to
get into the clinical implications – save this discussion for committee.
d. No
subgroup analysis is expected; the group discussed the value of how detailed
the characteristics reported in Table 1 might be. If there are unusual characteristics that
might affect the results (such as children receiving special services),
consider conducting a sensitivity test to see how much those subjects affected
the results.
e. Group
level results: the group discussed how to include raw and percentage scores in
a single table, and how the same information is presented in the narrative.
2.
Discussion:
Next semester’s meeting plan for CROW
a. Results
from Kairn’s Doodle Poll: change to Fridays, starting January 9, from 10:45 –
11:45.
3.
Next Workshop Meeting(s): Thursdays, 11:30 a.m.
– 12:45 p.m., at Given Courtyard South Level 4. Remember: the first 15 minutes are for
checking in with each other.
a.
Dec 18: Marianne: progress on IRB proposal and
recruitment methods (no Ben)
b.
Jan 9: Nancy– topic TBD
c.
Jan 16: Kairn – topic TBD
Friday, December 12, 2014
Cohorts for Heart and Aging Research in Epidemiology
Posted on behalf of Peter Durda
Cohorts for Heart and Aging Research in Epidemiology;
Investigator meeting
Translational Collaboration
Steven Cummings, M.D. University of California, San
Francisco
Dr. Cummings presented his thoughts on translational
collaborations and his history with these endeavors. Through his work as a principle investigator
of the Health, Aging, and Body Composition study (an NIH funded cohort) he has
been instrumental in leading the Longevity Consortium – a number of cohorts
studying the genetics of longevity and aging.
Dr. Cummings emphasized that collaborations are nothing more than
relationships; and they are tough and they take work. When scientists from different disciplines
are brought together they must overcome differing views on experimental design
and funding priorities as well as different languages. Epidemiologists, basic scientists, and
statisticians do not speak the same language and they need to understand each
other. Dr. Cummings sees future
mechanistic studies with basic scientist resulting from these consortia. Another point of emphasis of the talk was the
need to find/have alternative funding.
One example of private funding sources is Calico; a Google company
established in 2013 for the purpose of identifying drugs to extend
longevity. Calico will fund a ‘super’
cohort of >5000 participants over the age of 95. The two take home messages from this talk
were: 1) Translational collaboration involves hard work on relationships; and
2) There is a funding shift to private sources and there are funds available,
Dr. Cummings cited the Nature 2012 article entitled “Alternative funding:
Sponsor my science”.
Wednesday, December 10, 2014
Clinical Research Oriented Workshop (CROW) Meeting: Dec 4, 2014
Present: Marianne Burke, Sylvie Frisbie, Nancy Gell, Juvena
Hitt, Kairn Kelley, Amanda Kennedy, Ben Littenberg, Connie van Eeghen
Start Up:
(Connie was trapped in Hewlett-Packard land, and missed this.)
1.
Discussion Ben
Littenberg reviewed the PROMIS29 survey, planned as the primary outcome measure
of a PCORI research study for which the application is due in February.
a. The
survey read well, although the presentation of raw scores is hard to interpret
and may be misleading. Version 2 has
updated questions that include family and friends (matching a comment made in a
recent patient feedback group working on this grant).
b. The
T-scores present the percentiles related to the individual responses (not
the number of standard deviations from
the mean). However, these totals appear
to provide artificial ceilings and perhaps artificial floors for scores. (Ben later corrected this: the T-scores represent
a standardized score in 10ths of a sd with the mean set to 50. Given the
T-score, you get the percentile by looking it up in the cumulative normal
distribution.)
c. Ben
and Juvena to explore further. Face
validity is good, content flow decent, format acceptable; scoring is
mysterious. Further research needed:
website, NIH staff. Nancy has a colleague who might be of assistance.
2.
Discussion: Connie
shared the abstract of a manuscript in the process of a re-write after
re-running all the data. She shared 2
tables: description of patient-subjects (Table 3) and outcomes (Table 4).
a. Table
3 data, describing the underlying population, is unusual in that it compares
two time periods. Consider one table for
the 17 month period. Move the bottom row
(visits pppm) to the top of the result table.
b. The
12 month pre-window provides a conservative approach to assessing the change,
relative to the 5 month post-window. The
5 month post-window has a higher prevalence of older, sicker, and higher level
of visits (i.e. frequent flyers) than the 12 month window has.
c. Briefly
discuss the new Table 3, then focus the discussion on Table 4. Then discuss (without a new table) the changes
in the population attributed to the intervention.
d. Limitations:
secular changes induced by the intervention
e. Kaplan
Meier plots: makes the lines show up differently when viewed in black and white
f. Thank
you, everyone!
3.
Discussion:
Next semester’s meeting plan for CROW
a. Kairn
to send out DoodlePoll
4.
Next Workshop Meeting(s): Thursdays, 11:30 a.m.
– 12:45 p.m., at Given Courtyard South Level 4. Remember: the first 15 minutes are for
checking in with each other.
a.
Dec 11: Kairn: manuscript (no Ben)
b.
Dec 18: Marianne: data collection tools (no Ben)
c.
Jan 8: TBD
d.
Jan 15: TBD
Tuesday, December 2, 2014
PCP as secret therapist
Here's a NYT opinion piece, explaining the intricacies of PCP and young adult patients. Any reactions?
http://opinionator.blogs.nytimes.com/2014/12/01/the-secret-therapist/?hp&action=click&pgtype=Homepage&module=c-column-top-span-region®ion=c-column-top-span-region&WT.nav=c-column-top-span-region&_r=1
Connie
http://opinionator.blogs.nytimes.com/2014/12/01/the-secret-therapist/?hp&action=click&pgtype=Homepage&module=c-column-top-span-region®ion=c-column-top-span-region&WT.nav=c-column-top-span-region&_r=1
Connie
Wednesday, November 26, 2014
Report by Marianne Burke, PhD student
I
attended a presentation by Richard Platt MD, Chair of Population Health at Harvard
Pilgrim Health Care (HPHC) Institute, November 8 2014. Chicago Ill AAMC
Conference, Matheson Lecture entitled “On a Clear Day You Can See the Learning
Health System.”
Dr.
Platt discussed the work of the HPHC Institute as the Coordinating Center of the
National Patient-Centered Clinical Research Network funded with a 9 million
grant from PCORI (Patient Centered Clinical Research Institute). He introduced
the presentation by stating that there are so many patient care questions for
which there are no evidence-based answers, and that we (medical professionals)
have overestimated what we know. He stated that less than 15% of medical
guidelines are supported by firm evidence. Most are expert opinion or consensus
of practice. He made the case for finding the problems in large data
surveillance sets even as we try use these sets more often and try to combine
them to answer patient centered questions.
The
Matheson Lecture “at the juncture of Technology, Informatics and Medical
Library Science” occurs annually at AAMC (Association of American Medical
Colleges) co-sponsored by the AAMC Group on Information Resources and the
Association of Academic Health Sciences Libraries.
This
lecture was interesting and well-documented though not surprising to me as a
CTS student (of our excellent faculty) and medical librarian.
Wednesday, November 19, 2014
Clinical Research Oriented Workshop (CROW) Meeting: Nov 13, 2014
Present: Marianne Burke, Nancy Gell, Kairn Kelley (by
phone), Connie van Eeghen
Start Up:
Welcome Nancy! Nancy is a new
Assistant Professor in RMS, teaching in the PT program (public policy in Spring
2014; cardio-pulmonary – next year; health promotion – next year). Her
background is PT, Public Health – Health Behavior and Health Education,
Exercise Science.
1.
Discussion Marianne
Burke shared her updated draft application to the Lindberg Research Fellowship
offered by the Medical Library Association
a. Marianne
made many substantial changes regarding organization and language. We focused on grantsman(woman)ship issues:
b. Bring
out the applicant – make her easy to see.
Include voice, roles, and management responsibility (the grant pays for
research assistant(s)) as appropriate
c. Move
the goals of the research grant forward – it’s buried on the second page
d. Make
the language in the new diagram consistent with the narrative
e. Next
step: submission deadline is tomorrow – good luck!
2.
Next Workshop Meeting(s): Thursdays, 11:30 a.m.
– 12:45 p.m., at Given Courtyard South Level 4. Remember: the first 15 minutes are for
checking in with each other.
a.
Nov 20: Nancy – project proposal on physical activity
maintenance
b.
Nov 27: Thanksgiving! No CROW; eat turkey instead J
c.
Dec 4: Connie – manuscript: findings and discussion
Tuesday, November 11, 2014
Clinical Research Oriented Workshop (CROW) Meeting: Oct 30, 2014
Present: Marianne Burke, Kairn Kelley, Amanda Kennedy, Ben
Littenberg, Connie van Eeghen
Start Up:
(Missed this!)
1.
Discussion Marianne
Burke shared her draft application to the Lindberg Research Fellowship offered
by the Medical Library Association
a. Concise,
clear language
i.
Literature review
ii.
Significance – three specific ideas leading to the need
for evidence-based information about library-based services, using dermatology
because… leading to a cluster randomized trial. (Minimizes bias and strengthen
validity…)
1. Software
attached to outcomes
2. Library
services attached to outcomes
3. Cost
may be affected
b. Consistent
headings and outline form: help the reader understand, using terms from the application
instructions
i.
What each topic is (headers)
ii.
Flow of information: why this is important before what
the details are
c. Aims:
aims are broad; hypotheses are specific (e.g. there is no difference in time to
resolution for patients in the intervention group compared to patients in the
control group)
i.
One aim
ii.
Two hypotheses
d. Budget:
present the entire budget? Or just the
portion paid for by the fellowship?
e. Research
design:
i.
Sub-headings to support flow
ii.
Diagram of recruitment, randomization, patient visits,
recruitment, and interviews
f. Limitations:
watch for tone
g. Timeline:
make consistent with application; remember final report
h. Research
Dissemination Plan: this is a separate criterion in the reviewer’s
instructions. Buff this up!
i.
Next steps
i.
Letter of support (set up for Ben)
ii.
Revise
2.
Next Workshop Meeting(s): Thursdays, 11:30 a.m.
– 12:45 p.m., at Given Courtyard South Level 4. Remember: the first 15 minutes are for
checking in with each other.
a.
Oct 30: Marianne’s topic – doctoral fellowship
application(s)
b.
Nov 6: Connie to check with Ben on BHI data analysis
(No Marianne, Charlie, or Amanda)
c.
Nov 13: Marianne – grant applications
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