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June 2012 - American Association for Clinical Chemistry

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<strong>Clinical</strong><br />

Laboratory<br />

News<br />

eDiTorial sTaff<br />

editor—Nancy Sasavage, PhD<br />

senior editor—Genna Rollins<br />

senior editor—Bill Malone<br />

editorial assistant—Laura Kachin<br />

contributors—Hubert W. Vesper, PhD,<br />

and Julianne Cook Botelho, PhD<br />

boarD of eDiTors<br />

chair—Amy Saenger, PhD<br />

Mayo Clinic, Rochester, Minn.<br />

members—Lorin M. Bachmann, PhD, DABCC<br />

VCU Health System, Richmond, Va.<br />

Andrew Don-Wauchope, MD<br />

Juravinski Hospital and Cancer Center,<br />

Hamilton, Ontario<br />

Jacqueline Fisher<br />

Children’s Hospital Boston, Boston, Mass.<br />

Steven Goss, PhD<br />

Siemens Healthcare Diagnostics, Newark, Del.<br />

Pamela Steele, PhD<br />

Covance, Inc., Indianapolis, Ind.<br />

aacc officers<br />

President— W. Greg Miller, PhD, DABCC,<br />

FACB<br />

President-elect—Robert H. Christenson, PhD,<br />

DABCC, FACB<br />

Treasurer—D. Robert Dufour, MD<br />

secretary—Elizabeth L. Frank, PhD, DABCC,<br />

FACB<br />

Past-President—Ann Gronowski, PhD<br />

aDverTising sales<br />

Scherago International, Inc.<br />

525 Washington Blvd, Ste. 3310<br />

Jersey City, NJ 07310<br />

Phone: (201) 653-4777, Fax: (201) 653-5705<br />

E-mail: aacc@scherago.com<br />

President—H.L. Burklund<br />

v.P. of sales—Mike Minakowski<br />

sr. Director of sales & marketing<br />

—Steven A. Hamburger<br />

Traffic manager—Qien Porter<br />

subscriPTions<br />

<strong>American</strong> <strong>Association</strong> <strong>for</strong> <strong>Clinical</strong> <strong>Chemistry</strong>, Inc.<br />

1850 K Street, NW, Suite 625<br />

Washington, DC 20006<br />

Phone: (202) 857-0717 or (800) 892-1400<br />

Fax: (202) 887-5093<br />

E-mail: custserv@aacc.org<br />

Subscriptions to <strong>Clinical</strong> Laboratory News are<br />

free to qualified laboratory professionals in<br />

the United States. AACC members outside<br />

the U.S. pay $87 <strong>for</strong> postage. The subscription<br />

price <strong>for</strong> those who do not qualify <strong>for</strong> a free<br />

subscription is $87/year in the U.S. and $130/<br />

year outside the U.S. For more in<strong>for</strong>mation,<br />

contact the AACC Customer Service Department<br />

at (800) 892-1400 or (202) 857-0717 or<br />

custserv@aacc.org.<br />

eDiTorial corresPonDence<br />

Nancy Sasavage, PhD, Editor<br />

<strong>Clinical</strong> Laboratory News<br />

1850 K Street, NW, Suite 625<br />

Washington, DC 20006<br />

Phone: (202) 835-8725 or (800) 892-1400<br />

Fax: (202) 835-8725<br />

E-mail: nsasavage@aacc.org<br />

Contents copyright © <strong>2012</strong> by the <strong>American</strong><br />

<strong>Association</strong> <strong>for</strong> <strong>Clinical</strong> <strong>Chemistry</strong>, Inc.,<br />

except as noted. Printed in the U.S.A.<br />

<strong>Clinical</strong> laboratory news (issn 0161-9640)<br />

is the authoritative source <strong>for</strong> timely analysis<br />

of issues and trends affecting clinical<br />

laboratories, clinical laboratorians, and the<br />

practice of clinical laboratory science.<br />

@cln_aacc<br />

4 CliniCal laboratory news <strong>June</strong> <strong>2012</strong><br />

Few Understand the Evidence<br />

screening Tests, continued from page 3<br />

and patients had completely ignored the<br />

USPSTF recommendation.<br />

Patients’ enthusiasm alone may not be<br />

to blame <strong>for</strong> such a discrepancy between<br />

recommendations and practice. There also<br />

is reason to doubt that physicians themselves<br />

can comprehend or communicate<br />

even the basic facts about evidence when<br />

it comes to screening tests. A nationally<br />

representative survey of internal medicine<br />

physicians found that a majority were easily<br />

stumped by questions about basic statistics<br />

and would recommend a screening test<br />

to save lives based on irrelevant evidence<br />

(Ann Intern Med <strong>2012</strong>;156:340–349).<br />

The researchers expected that physicians<br />

would understand that in screening<br />

tests, survival statistics are susceptible to<br />

lead-time and overdiagnosis biases. In fact,<br />

more than 20 years ago the National Cancer<br />

Institute concluded that reduced mortality<br />

in a randomized trial could be the<br />

only reliable evidence that a screening test<br />

saved lives. However, when presented with<br />

evidence about two hypothetical screening<br />

tests, physicians in the study overwhelmingly<br />

favored a test backed by evidence of<br />

improved 5-year survival over one with an<br />

improved mortality rate.<br />

The inability of some physicians to interpret<br />

data about screening tests appears<br />

even more dire considering how USPSTF<br />

and other groups have leaned toward optional<br />

shared decision-making in their recommendations.<br />

This concept emphasizes<br />

the importance of doctor-patient collaboration<br />

to arrive at healthcare decisions and<br />

puts greater emphasis on patient autonomy<br />

and choice. The concept gained momentum<br />

especially with PSA testing after<br />

USPSTF’s 2008 “I” recommendation <strong>for</strong><br />

prostate cancer screening in men younger<br />

than 75, which suggested that these men<br />

“should be assisted in considering their personal<br />

preferences be<strong>for</strong>e deciding whether<br />

to be tested.”<br />

Many opinion leaders in healthcare<br />

expressed deep frustration with this strategy,<br />

questioning shared decision-making<br />

<strong>for</strong> controversial screening tests <strong>for</strong> which<br />

the evidence perplexes both doctors and<br />

patients. For example, Allan Brett, MD, is<br />

among those who welcomed USPSTF’s<br />

more conservative 2011 draft recommendations<br />

against using PSA tests to screen <strong>for</strong><br />

prostate cancer.<br />

After those draft recommendations<br />

were published, Brett, a professor of medicine<br />

at the University of South Carolina<br />

School of Medicine and member of the<br />

university’s Center <strong>for</strong> Bioethics and Medical<br />

Humanities, wrote an editorial praising<br />

USPSTF <strong>for</strong> giving physicians clearer guidance<br />

(N Engl J Med 2011; 365:1949–1951).<br />

“For two decades, primary care physicians<br />

have been expected to present a flawed<br />

online extra<br />

low-value scenarios<br />

<strong>for</strong> lab Tests<br />

go to the <strong>June</strong> issue<br />

of CLN at<br />

www.aacc.org<br />

screening test to patients, cloaking the flaws<br />

in an elaborate ritual of in<strong>for</strong>med decision<br />

making. In turn, men have been expected<br />

to make sense of a confusing mix of hypothetical<br />

outcomes,” he wrote. Due to the<br />

difficulty of digesting the data on screening,<br />

these patient-physician discussions about<br />

PSA testing were “essentially a charade,”<br />

and their decisions “reflected their general<br />

concerns about cancer or their general inclination<br />

to accept or resist medical interventions.”<br />

Brett is also the editor-in-chief of<br />

Journal Watch General Medicine.<br />

Brett also recently wrote about coping<br />

with patient pressure <strong>for</strong> unnecessary tests<br />

and procedures more generally (JAMA<br />

<strong>2012</strong>;307:149–150). Physicians have been<br />

overcorrecting <strong>for</strong> their traditionally paternalistic<br />

tendencies since the 1980s, he<br />

argued. Now the pendulum has swung too<br />

far, with physicians’ intellectual authority<br />

routinely questioned. “Yes, there should be<br />

a partnership between doctors and patients<br />

in decision-making, but when it crosses the<br />

boundary into things that don’t plausibly<br />

confer medical benefit, physicians should<br />

be able to say no,” he told CLN.<br />

These pressures on physicians are one<br />

reason that Harris advocates the use of outcomes<br />

tables that do a better job of capturing<br />

all of the potential benefits and harms<br />

of a particular screening test. “If you don’t<br />

lay it out <strong>for</strong> people, it’s hard <strong>for</strong> them to<br />

see what is meant by harms,” he said. “We<br />

need to help people see that the benign<br />

blood test that you agree to when you have<br />

a doctor visit can end up being the first step<br />

in a cascade of events that, after a while, you<br />

won’t be able to control. And that cascade<br />

can end up with your being helped, but it<br />

might also result in your being hurt.”<br />

But is it possible that giving patients<br />

more choices can boost screening where<br />

underutilization is a problem? New evidence<br />

suggests that in the case of colon<br />

cancer screening, offering patients choices<br />

about the type of test boosted compliance<br />

(Arch Intern Med <strong>2012</strong>;172:575–582). The<br />

researchers viewed these results as particularly<br />

significant because patients frequently<br />

avoid recommended colon cancer screening.<br />

They found that patients <strong>for</strong> whom<br />

colonoscopy was recommended were less<br />

likely to complete colorectal cancer screening<br />

than either those <strong>for</strong> whom FOBT was<br />

recommended or those who were given<br />

a choice between FOBT or colonoscopy.<br />

Only 38.2% of the participants in the colonoscopy<br />

group completed that procedure,<br />

compared with 67.2% in the FOBT group<br />

and 68.8% of those allowed to choose their<br />

own screening method.<br />

In an invited commentary on the study,<br />

Theodore Levin, MD, urged physicians to<br />

See screening Tests, continued on page 6<br />

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