Bill Text: HI SB2885 | 2016 | Regular Session | Amended


Bill Title: Birth Defects Program; Use of Data

Spectrum: Partisan Bill (Democrat 1-0)

Status: (Passed) 2016-04-26 - Act 020, on 04/26/2016 (Gov. Msg. No. 1120). [SB2885 Detail]

Download: Hawaii-2016-SB2885-Amended.html

THE SENATE

S.B. NO.

2885

TWENTY-EIGHTH LEGISLATURE, 2016

S.D. 1

STATE OF HAWAII

 

 

 

 

 

 

A BILL FOR AN ACT

 

 

RELATING TO BIRTH DEFECTS.

 

 

BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF HAWAII:

 


     SECTION 1.  Section 324-43, Hawaii Revised Statutes, is amended to read as follows:

     "[[]§324-43[]]  Use of collected information.  (a)  The information collected under this part shall be used by the department of health or researchers only for the purpose of advancing medical and public health research, medical education, or education of the public and healthcare providers in the interest of reducing morbidity or mortality[,] or increasing physicians' knowledge of resources available for families of persons with birth defects, and only as approved or exempted by an institutional review board.

     (b)  The identity of, or any information which alone or in combination with other reasonably available information that may be used to identify, any person whose condition or treatment has been studied under this part shall be confidential.

     (c)  If the [[]birth defects program[]] or researchers intend to collect additional information directly from a patient or patient's relative for research studies approved by an institutional review board, the researcher shall first obtain approval for the request from the patient's [attending physician.] primary care provider.  If the patient's current physician is not known, the patient may be contacted directly using a method approved by an institutional review board.  The use of the additional information obtained by researchers shall be governed by subsection (a)."

     SECTION 2.  Statutory material to be repealed is bracketed and stricken.  New statutory material is underscored.

     SECTION 3.  This Act shall take effect on July 1, 2016.

 


 


 

Report Title:

Birth Defects Program; Use of Data

 

Description:

Authorizes the use of birth defects data for education of health care providers to reduce morbidity or mortality and to increase physicians' knowledge of resources available for families of persons with birth defects.  (SD1)

 

 

 

The summary description of legislation appearing on this page is for informational purposes only and is not legislation or evidence of legislative intent.

 

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