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Industry News: Other Healthcare News

Tuesday, January 31, 2012

Representatives from the College of American Pathologists met with CMS to express concerns regarding the Molecular Diagnostics (MolDx) reporting program announced by Palmetto GBA in November 2011, and asked CMS to delay or revoke the program. Palmetto's adoption of the Z-codes amounts to the creation of a local coding system, which violates the Health Information Portability Act (HIPAA), CAP leaders told CMS during the meeting.

Tuesday, November 01, 2011

The Medical Group Management Association (MGMA) is calling on the Department of Health and Human Services (HHS) to issue a HIPAA 5010 contingency plan permitting health plans to adjudicate claims that may not have all the required data.

MGMA’s research suggests that critical coordination among many practices and their trading partners has not yet occurred. Practices that do not successfully implement Version 5010 by the Jan. 1, 2012, compliance date face possible disruption in cash flow, say experts.

Thursday, September 22, 2011

According to a recent policy update, CIGNA announces that it will adopt a common time frame for all health care providers to follow when submitting claims. Except where state law requires a longer time frame, the claim filing limit will change from 180 days to 90 days for participating health care professionals. Currently, over 99 percent of CIGNA claims are already submitted within this time frame.

Thursday, September 22, 2011

The BlueCard Program links participating healthcare providers and the independent Blue Cross and Blue Shield Plans across the country, as well as more than 200 countries and territories, through a single electronic network for claims processing and reimbursement.

Labs have submitted all Blue Cross and Blue Shield claims to their local service area plan and the local plan moves the claim to the BlueCard network for processing.

Wednesday, September 21, 2011

The Molecular Pathology Workgroup will meet on Thursday, Oct 13, 2011. The meeting is scheduled for 3:30 pm (CST) in the Chicago D & E Ballroom of the Chicago Marriott Hotel, 540 N. Michigan Avenue, Chicago, IL.

Thursday, July 28, 2011

As the deadline for HIPAA version 5010 looms around the corner on January 1, 2012, demand for information on ICD-10 implementation and risk mitigation continues to escalate. Healthcare Information and Management Systems Society (HIMSS), along with 29 plus participating organizations consisting of associations, providers, health plans, vendors, clearing houses, financial institutions, work force solutions groups and a host of leading industry stakeholders, launched the ICD-10 PlayBook on May 25.

Monday, July 25, 2011

XIFIN is pleased to announce the creation of the XIFIN 5010 community on LinkedIn.  This new group focuses on the payors and their readiness for 5010 submissions, remittance and communications testing.  Payors, vendors, facilities and practices can monitor, generate and participate in discussions related to payor testing challenges and status.   

Friday, May 27, 2011

Washington is the latest state to enact direct billing legislation for anatomic pathology (AP) services. The legislation, signed into law April 20, will ensure that patients are billed for AP service only by the physician who performs or supervises the service. Similar legislation is pending in Indiana, and if approved, Indiana would become the 18th state with a direct billing law.

Monday, May 02, 2011

What Is HCPCS?

The Centers for Medicare and Medicaid Services (CMS) created the HCPCS. It is a collection of codes and descriptors that represent procedures, supplies, products and services that may be provided to Medicare beneficiaries and to patients enrolled in private health insurance programs. The codes are divided into two levels.

Saturday, March 19, 2011

Centers for Medicare and Medicaid Services (CMS), has rescinded its original directive requiring physician signatures for all Medicare orders of clinical diagnostic laboratory services paid on the CLFS that would have become effective on 4/1/2011.

If you wish to monitor physician compliance with a signature on an order for record keeping purposes, you may still use the Signature tracking functionality within the XIFIN system.

Monday, January 31, 2011

On December 18, 2010, the President signed into law the "Red Flag Program Clarification Act of 2010," which clarifies the type of "creditor" that must comply with the Red Flags Rule. The AMA is pleased that this law supports AMA’s long-standing argument to the Federal Trade Commission (FTC) that the Red Flags Rule should not be applied to physicians generally.

Monday, November 22, 2010

Most pathologists and clinical laboratory managers are not aware that implementation of global location numbers (GLNs) will occur in just a few months. Every healthcare provider in the United States and many other nations will get a unique GLN.

Friday, October 01, 2010

The Department of Health and Human Services has unveiled CuidadodeSalud.gov, the first website of its kind in Spanish to connect consumers to new information and resources aimed at helping them access quality, affordable healthcare coverage.

HHS announced the launch on Sept. 8.

Friday, October 01, 2010

Pathologists and clinical laboratory managers will soon have a comprehensive registry of genetic tests that they can consult as needed. The National Institutes of Health (NIH) is creating a single public registry with detailed information about both genetic test providers and the 1,600+ genetic tests these providers offer.

The NIH believes the genetic test registry will bring greater transparency to the field. It hopes that the registry creates increased information-sharing about the different genetic tests which are available. Participation in the registry will be voluntary.

Wednesday, September 01, 2010

In a letter dated June 15, 2010, COLA provided official notice of its intent to voluntarily withdraw from accreditation in the specialty of Pathology. This withdrawal was effective June 30, 2010. All laboratories accredited by COLA in the specialty of Pathology (to include Histopathology, Oral Pathology or Cytology) will have 60 days from the date of this Federal Register notice to seek either CLIA inspection by the State Agency where the laboratory is located or accreditation with another accrediting organization that is currently CMS-approved for the specialty of Pathology.

Friday, August 13, 2010

A recently launched federal website, www.healthcare.gov, provides consumers with information about private and public health coverage options, tailored specifically for their needs in a single, easy-to-use tool. In addition, the website will be a one-stop-shop for information about the implementation of the Affordable Care Act and other health care resources.

Tuesday, November 24, 2009

At the Executive War College this year in New Orleans, we invited 10 laboratory industry top executives to join us to examine the data and insights in a round table discussion format. The net result was a positive dialog about benchmarks, trends, and industry best in class results. At the conclusion of the round table, the consensus from the group was that the information was valuable and that it would be useful to see the same data on a regular basis with a forum for discussion.