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 <dateIssued encoding="w3cdtf">1998-09-24</dateIssued>
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<classification authority="sudocs">GA 1.13:T-AIMD-98-310</classification>
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 <subject>Y2K</subject>
 <subject>Strategic information systems planning</subject>
 <subject>Systems compatibility</subject>
 <subject>Medical equipment</subject>
 <subject>Health care services</subject>
 <subject>Medical information systems</subject>
 <subject>Systems conversions</subject>
 <subject>Computer software verification and validation</subject>
 <subject>Computer software</subject>
 <subject>Embedded computer systems</subject>
 <identifier>VA Year 2000 Strategy</identifier>
 <identifier>VA Veterans Integrated Service Network</identifier>
 <identifier>Y2K</identifier>
 <identifier>Magnetic Resonance Imaging</identifier>
 <type>Testimony</type>
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<titleInfo>
 <title>Year 2000 Computing Crisis: Leadership Needed to Collect and Disseminate Critical Biomedical Equipment Information</title>
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<abstract>Biomedical equipment that relies on computers or computer chips, from
cardiac monitoring systems to electronic imaging machines, may be
adversely affected by the Year 2000 problem. Although this situation has
serious implications for the delivery of health care to the nation&apos;s
veterans, the Veterans Health Administration (VHA) still does not know
the full extent of its Year 2000 problem or the cost to overcome it.
This is because it has yet to receive compliance information from 27
percent of the biomedical equipment manufacturers on its list of
suppliers or from the nearly 100 other manufacturers that VHA discovered
were no longer in business. According to VHA, most manufacturers
reporting noncompliant equipment cited incorrect display of date or time
as problems--albeit ones that health care providers can work around.
Some manufacturers, however, cited more serious problems that could
jeopardize patient safety. For example, a miscalculation by a radiation
therapy planning computer could cause a patient to receive a hazardous
radiation dose. The Food and Administration (FDA), which oversees and
regulates medical devices, has sent letters to biomedical equipment
manufacturers asking for information on products affected by the Year
2000 problem. The response rate to FDA has been disappointing. It is
critical that such information be obtained and publicized. This
testimony summarizes the September 1998 report, GAO/AIMD-98-240.</abstract>
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<note>Testimony</note>
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<subject>
 <topic>Y2K</topic>
 <topic>Strategic information systems planning</topic>
 <topic>Systems compatibility</topic>
 <topic>Medical equipment</topic>
 <topic>Health care services</topic>
 <topic>Medical information systems</topic>
 <topic>Systems conversions</topic>
 <topic>Computer software verification and validation</topic>
 <topic>Computer software</topic>
 <topic>Embedded computer systems</topic>
 <topic>VA Year 2000 Strategy</topic>
 <topic>VA Veterans Integrated Service Network</topic>
 <topic>Y2K</topic>
 <topic>Magnetic Resonance Imaging</topic>
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