HAR §16-12-12.6
HAR §16-12-12.6. Reporting of multiple policies
Cite as Haw. Code R. § 16-12-12.6
(a)
On or before March 1 of each year, an issuer shall
report to the commissioner in substantially the form
entitled Appendix B (Exhibit B (revised 2019)),
located at the end of this chapter, which is made a
part of this section, the following information for
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every individual resident of this State for which the
issuer has in force more than one Medicare supplement
policy or certificate:
(1)
Policy and certificate number; and
(2)
Date of issuance.
(b)
The items set forth in subsection (a) shall
be grouped by individual policyholder. [Eff and comp
12/27/90; am and comp 9/3/92; am and comp 7/6/99; comp
10/15/01; comp 12/9/02; comp 10/8/05; am and comp
9/25/09; am and comp 8/1/19] (Auth: HRS §§431:2-201,
431:10A-305, 431:10A-307, 431:10A-309) (Imp: HRS
§§431:2-201, 431:10A-305, 431:10A-307, 431:10A-309)
§16-12-12.8 Prohibition against preexisting
conditions, waiting periods, elimination periods, and
probationary periods in replacement policies or
certificates. (a) If a Medicare supplement policy or
certificate replaces another Medicare supplement
policy or certificate, the replacing issuer shall
waive any time periods applicable to preexisting
conditions, waiting periods, elimination periods, and
probationary periods in the new Medicare supplement
policy or certificate for similar benefits to the
extent that time was spent under the original policy.
(b)
If a Medicare supplement policy or
certificate replaces another Medicare supplement
policy or certificate which has been in effect for at
least six months, the replacing policy or certificate
shall not provide any time period applicable to
preexisting conditions, waiting periods, elimination
periods, and probationary periods for benefits similar
to those contained in the original policy or
certificate. [Eff and comp 12/27/90; am and comp
9/3/92; comp 7/6/99; comp 10/15/01; comp 12/9/02; am
and comp 10/8/05; comp 9/25/09; am and comp 8/1/19]
(Auth: HRS §§431:2-201, 431:10A-304, 431:10A-305)
(Imp: HRS §§431:2-201, 431:10A-304, 431:10A-305)
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§16-12-12.9 Prohibition against use of genetic
information and requests for genetic testing. (a)
This section applies to all policies with policy years
beginning on or after May 21, 2009.
(b)
An issuer of a Medicare supplement policy or
certificate:
(1)
Shall not deny or condition the issuance or
effectiveness of the policy or certificate
(including the imposition of any exclusion
of benefits under the policy based on a
preexisting condition) on the basis of the
genetic information with respect to such
individual; and
(2)
Shall not discriminate in the pricing of the
policy or certificate (including the
adjustment of premium rates) of an
individual on the basis of the genetic
information with respect to such individual.
(c)
Nothing in subsection (b) shall be construed
to limit the ability of an issuer, to the extent
otherwise permitted by law, from:
(1)
Denying or conditioning the issuance or
effectiveness of the policy or certificate
or increasing the premium for a group based
on the manifestation of a disease or
disorder of an insured or applicant; or
(2)
Increasing the premium for any policy issued
to an individual based on the manifestation
of a disease or disorder of an individual
who is covered under the policy (in such
case, the manifestation of a disease or
disorder in one individual cannot also be
used as genetic information about other
group members and to further increase the
premium for the group).
(d)
An issuer of a Medicare supplement policy or
certificate shall not request or require an individual
or a family member of such individual to undergo a
genetic test.
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(e)
Subsection (d) shall not be construed to
preclude an issuer of a Medicare supplement policy or
certificate from obtaining and using the results of a
genetic test in making a determination regarding
payment (as defined for the purposes of applying the
regulations promulgated under part C of title XI and
Section 264 of the Health Insurance Portability and
Accountability Act of 1996, as may be revised from
time to time) and consistent with subsection (b).
(f)
For purposes of carrying out subsection (e),
an issuer of a Medicare supplement policy or
certificate may request only the minimum amount of
information necessary to accomplish the intended
purpose.
(g)
Notwithstanding subsection (d), an issuer of
a Medicare supplement policy may request, but not
require, that an individual or a family member of such
individual undergo a genetic test if each of the
following conditions is met:
(1)
The request is made pursuant to research
that complies with part 46 of title 45, Code
of Federal Regulations, or equivalent
federal regulations, and any applicable
state or local law or regulations for the
protection of human subjects in research.
(2)
The issuer clearly indicates to each
individual, or in the case of a minor child,
to the legal guardian of such child to whom
the request is made that:
(A)
Compliance with the request is
voluntary; and
(B)
Non-compliance will have no effect on
enrollment status or premium or
contribution amounts.
(3)
No genetic information collected or acquired
under this subsection shall be used for
underwriting, determination of eligibility
to enroll or maintain enrollment status,
premium rates, or the issuance, renewal, or
replacement of a policy or certificate.
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(4)
The issuer notifies the commissioner in
writing that the issuer is conducting
activities pursuant to the exception
provided for under this subsection,
including a description of the activities
conducted.
(5)
The issuer complies with such other
conditions as the commissioner may by rule
require for activities conducted under this
subsection.
(h)
An issuer of a Medicare supplement policy or
certificate shall not request, require, or purchase
genetic information for underwriting purposes.
(i)
An issuer of a Medicare supplement policy or
certificate shall not request, require, or purchase
genetic information with respect to any individual
prior to such individual's enrollment under the policy
in connection with such enrollment.
(j)
If an issuer of a Medicare supplement policy
or certificate obtains genetic information incidental
to the requesting, requiring, or purchasing of other
information concerning any individual, such request,
requirement, or purchase shall not be considered a
violation of subsection (i) if such request,
requirement, or purchase is not in violation of
subsection (h).
(k)
For the purposes of this section only:
(1)
"Issuer of a Medicare supplement policy or
certificate" includes a third-party
administrator or other person acting for or
on behalf of such issuer.
(2)
"Family member" means, with respect to an
individual, any other individual who is a
first-degree, second-degree, third-degree,
or fourth-degree relative of such
individual.
(3)
"Genetic information" means, with respect to
any individual, information about such
individual's genetic tests, the genetic
tests of family members of such individual,
and the manifestation of a disease or
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disorder in family members of such
individual. Such term includes, with
respect to any individual, any request for,
or receipt of, genetic services, or
participation in clinical research which
includes genetic services, by such
individual or any family member of such
individual. Any reference to genetic
information concerning an individual or
family member of an individual who is a
pregnant woman, includes genetic information
of any fetus carried by such pregnant woman,
or with respect to an individual or family
member utilizing reproductive technology,
includes genetic information of any embryo
legally held by an individual or family
member. The term "genetic information" does
not include information about the sex or age
of any individual.
(4)
"Genetic services" means a genetic test,
genetic counseling (including obtaining,
interpreting, or assessing genetic
information), or genetic education.
(5)
"Genetic test" means an analysis of human
DNA, RNA, chromosomes, proteins, or
metabolites, that detect genotypes,
mutations, or chromosomal changes. The term
"genetic test" does not mean an analysis of
proteins or metabolites that does not detect
genotypes, mutations, or chromosomal
changes; or an analysis of proteins or
metabolites that is directly related to a
manifested disease, disorder, or
pathological condition that could reasonably
be detected by a health care professional
with appropriate training and expertise in
the field of medicine involved.
(6)
"Underwriting purposes" means:
(A)
Rules for, or determination of,
eligibility (including enrollment and
continued eligibility) for benefits
under the policy;
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(B)
The computation of premium or
contribution amounts under the policy;
(C)
The application of any preexisting
condition exclusion under the policy;
and
(D)
Other activities related to the
creation, renewal, or replacement of a
contract of health insurance or health
benefits. [Eff and comp 9/25/09; am
and comp 8/1/19] (Auth: HRS
§§431:2-201, 431:10A-304, 431:10A-305)
(Imp: HRS §§431:2-201, 431:10A-304,
431:10A-305, 431:10A-309)