[{"innerBlocks":[],"name":"core\/freeform","postId":2804,"blockType":{"name":"core\/freeform","keywords":[],"attributes":{"content":{"type":"string","source":"raw"},"lock":{"type":"object"}},"providesContext":[],"usesContext":[],"selectors":[],"supports":{"className":false,"customClassName":false,"reusable":false},"styles":[],"variations":[],"apiVersion":3,"title":"Classic","description":"Use the classic WordPress editor.","category":"text"},"originalContent":"The shift to the new administration in Washington has changed the approach for achieving regulatory guidance for healthcare information technology.

The number of regulations and rules descending from federal agencies is way down, says Liz Johnson, vice president and CIO of acute care hospitals and applied clinical informatics for Tenet Healthcare.

An executive order from President Donald Trump is part of the reason, said Johnson, chair of the board of trustees for the College of Healthcare Information Management Executives (CHIME). One of the many orders he has signed has required federal agencies to eliminate two regulations for every new one that\u2019s created.

\u201cSo that\u2019s working really well; we have no new regulations,\u201d Johnson quipped at a session Thursday at the CHIME17 Fall CIO Forum in San Antonio. The idea behind the order was to ease regulatory burdens, which have been particularly crushing to providers in general and IT operations in particular.

Also See:<\/b> Why text and email use face a host of regulatory constraints<\/a>

\u201cAll the rules we\u2019ve faced have created more overhead for us, and we really can\u2019t take much more,\u201d she said.

Budget constraints also are limiting the bandwidth of federal agencies such as the Office of the National Coordinator for Health Information Technology, which saw its Fiscal Year 2018 budget slashed by 39 percent from the $60 million it received in FY 2017.

\u201cThat\u2019s clearly going to indicate a change in ONC\u2019s scope,\u201d Johnson said.

For example, in testimony before a Congressional panel this week, Jon White, MD, deputy national coordinator for health IT, noted that ONC would not be able to meet one of the requirements of the Cures Act, a provision that calls for a transparent process to develop criteria as part of an \u201cEHR Reporting Program\u201d for certified health IT.

Other challenges await the health IT industry as the Food and Drug Administration is relaxing its oversight of mobile apps; Johnson contends that providers could bear the brunt of the risk for data breaches involving apps, even as it\u2019s facing increasing pressure to give consumers access to more healthcare information through use of apps.

\u201cWashington is still very divided\u2014today, we don\u2019t even see solidarity within the parties,\u201d she said. \u201cWe need them to stabilize so we know what they\u2019re going to do so we can move forward. This has impacted our ability to predict what\u2019s going to happen and thus what we need to do.\u201d

Recent pronouncements out of Washington have been good for the industry, Johnson said, highlighting the decision to not require providers to meet Stage 3 of the Meaningful Use Program in 2018, and setting 90 day reporting periods for the year instead of reporting on the entire 365 days of the year.

CHIME advocacy staff and organizational leaders will be looking for further guidance on the recently announced plan by CMS to move to a program involving meaningful measures. While no details have been released, it appears the approach could reduce the regulatory burden on providers while increasing the utility of the measures involved.
","saveContent":"The shift to the new administration in Washington has changed the approach for achieving regulatory guidance for healthcare information technology.

The number of regulations and rules descending from federal agencies is way down, says Liz Johnson, vice president and CIO of acute care hospitals and applied clinical informatics for Tenet Healthcare.

An executive order from President Donald Trump is part of the reason, said Johnson, chair of the board of trustees for the College of Healthcare Information Management Executives (CHIME). One of the many orders he has signed has required federal agencies to eliminate two regulations for every new one that\u2019s created.

\u201cSo that\u2019s working really well; we have no new regulations,\u201d Johnson quipped at a session Thursday at the CHIME17 Fall CIO Forum in San Antonio. The idea behind the order was to ease regulatory burdens, which have been particularly crushing to providers in general and IT operations in particular.

Also See:<\/b> Why text and email use face a host of regulatory constraints<\/a>

\u201cAll the rules we\u2019ve faced have created more overhead for us, and we really can\u2019t take much more,\u201d she said.

Budget constraints also are limiting the bandwidth of federal agencies such as the Office of the National Coordinator for Health Information Technology, which saw its Fiscal Year 2018 budget slashed by 39 percent from the $60 million it received in FY 2017.

\u201cThat\u2019s clearly going to indicate a change in ONC\u2019s scope,\u201d Johnson said.

For example, in testimony before a Congressional panel this week, Jon White, MD, deputy national coordinator for health IT, noted that ONC would not be able to meet one of the requirements of the Cures Act, a provision that calls for a transparent process to develop criteria as part of an \u201cEHR Reporting Program\u201d for certified health IT.

Other challenges await the health IT industry as the Food and Drug Administration is relaxing its oversight of mobile apps; Johnson contends that providers could bear the brunt of the risk for data breaches involving apps, even as it\u2019s facing increasing pressure to give consumers access to more healthcare information through use of apps.

\u201cWashington is still very divided\u2014today, we don\u2019t even see solidarity within the parties,\u201d she said. \u201cWe need them to stabilize so we know what they\u2019re going to do so we can move forward. This has impacted our ability to predict what\u2019s going to happen and thus what we need to do.\u201d

Recent pronouncements out of Washington have been good for the industry, Johnson said, highlighting the decision to not require providers to meet Stage 3 of the Meaningful Use Program in 2018, and setting 90 day reporting periods for the year instead of reporting on the entire 365 days of the year.

CHIME advocacy staff and organizational leaders will be looking for further guidance on the recently announced plan by CMS to move to a program involving meaningful measures. While no details have been released, it appears the approach could reduce the regulatory burden on providers while increasing the utility of the measures involved.
","order":0,"get_parent":{},"attributes":[],"attributesType":{"content":{"type":"string","source":"raw"},"lock":{"type":"object"}},"dynamicContent":""}]

Reductions in regulations are a mixed bag for HIT

More for you