Assembly Actions -
Lowercase Senate Actions - UPPERCASE |
|
---|---|
Jan 06, 2010 |
referred to insurance |
Feb 23, 2009 |
referred to insurance |
Assembly Bill A5918
2009-2010 Legislative Session
Sponsored By
TOWNS
Archive: Last Bill Status - In Assembly Committee
- Introduced
-
- In Committee Assembly
- In Committee Senate
-
- On Floor Calendar Assembly
- On Floor Calendar Senate
-
- Passed Assembly
- Passed Senate
- Delivered to Governor
- Signed By Governor
Actions
2009-A5918 (ACTIVE) - Details
- Current Committee:
- Assembly Insurance
- Law Section:
- Insurance Law
- Laws Affected:
- Amd §§3216, 3221 & 4303, Ins L
- Versions Introduced in 2011-2012 Legislative Session:
-
A5464
2009-A5918 (ACTIVE) - Bill Text download pdf
S T A T E O F N E W Y O R K ________________________________________________________________________ 5918 2009-2010 Regular Sessions I N A S S E M B L Y February 23, 2009 ___________ Introduced by M. of A. TOWNS, DenDEKKER, RAIA -- read once and referred to the Committee on Insurance AN ACT to amend the insurance law, in relation to requiring health insurance policies to cover the cost of equipment, supplies and tests for the diagnosis and treatment of thalassemia, or Cooley's anemia, and relating to the medicaid buy-in program for people with thalasse- mia THE PEOPLE OF THE STATE OF NEW YORK, REPRESENTED IN SENATE AND ASSEM- BLY, DO ENACT AS FOLLOWS: Section 1. Legislative findings and intent. The legislature finds and declares that the cost of medical care in the United States has steadily risen in the last five years, outpacing both employer wages and inflation. Chronic disease consumes approximately seventy-eight percent of health expenditures. Patients with thalassemia, an inherited blood disorder, require frequent red blood cell transfusions and iron chela- tion therapy for survival. Patients with thalassemia are the largest chronic consumers of blood in the United States. Patients surveyed in New York state claim their out-of-pocket costs average $555 per month. Eighty-five percent of patients with thalassemia pay between 3 to 5 co-pays per month, with co-pays ranging from $15 to $30 a visit. Nearly fifty percent of patients contributed a portion to their employer's payment of premiums or paid their health insurance premiums outright. Fifty percent of the patients surveyed had deductibles greater than $1,000 that had to be satisfied before coverage began. Patients with thalassemia require numerous prescription drugs, on average between 3 to 4 prescription drugs a month with the average cost to the patient, rang- ing between $150 to $200 a month. The legislature therefore finds that with new treatments being expensive and for those with 50 percent co-in- surance on prescription drugs, with the average cost being $1,500 a month, it would benefit residents of the state to require health insur- ance policies to cover the cost of equipment, supplies and tests for the EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets [ ] is old law to be omitted. LBD08607-01-9
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