Current through Register Vol. 51, No. 19, September 20, 2024
A. Patients admitted to facilities shall be
screened for hearing impairment.
B.
Gross Testing of Hearing Sensitivity.
(1) At
each facility, an examination shall be performed for gross testing of hearing
sensitivity on all newly admitted patients within 24 hours of admission. This
examination shall be performed:
(a) By a
physician or a qualified allied health professional; and
(b) According to the following protocol:
(i) Testing shall occur consistently at a
fixed distance from the speaker at all times;
(ii) In order to prevent speech reading which
could be interpreted as a false positive, the speaker's face may not be in view
by the patient while testing is in process; and
(iii) Non-English speaking patients shall be
tested in the language the patient is known to speak or is believed to
comprehend.
(2) Testing performed in conformance with
§B(1) of this regulation shall be repeated within 15 days after admission
on all patients not already tested with a pure tone screening
audiometer.
(3) Each test performed
in compliance with this regulation shall be documented in the patient's
chart.
(4) Once a hearing
impairment is suspected:
(a) Rinne and Weber
testing shall be performed; and
(b)
Referral shall be made for audiometric screening.
C. Audiometric Screening.
(1) Patients with Suspected Hearing
Impairment.
(a) Pure tone audiometric
screening shall occur within 3 working days from the period specified in
§B(1), of this regulation, for any patient who:
(i) Is suspected of having a hearing
impairment on the basis of any of the above tests;
(ii) Was unresponsive because of a possible
hearing impairment; or
(iii)
Responded in a manner that may be construed as a mental disorder, but may be
confused with a possible hearing impairment.
(b) Patients suspected of having a hearing
impairment on the basis of the latest pure tone audiometric screening shall be
referred promptly but in not more than 5 working days to an audiologist or an
otolaryngologist. Referral shall be documented in the patient's
chart.
(c) Upon recommendation by
either the otolaryngologist or audiologist, further evaluation by a
speech-language pathologist shall be conducted.
(d) If the audiometric screening in this
section is used as the initial screening test, that audiometric screening shall
be sufficient testing on admission unless otherwise ordered.
(2) Patients Not Identified as
Hearing Impaired. As soon as possible, but within 90 days after admission, each
patient who has not already been screened with an audiometer shall be so
evaluated.
(3) Each patient's
annual physical examination shall include audiometric screening. The screening
results shall be documented in the patient's chart.
(4) Procedures for Audiometric Screening.
(a) The audiometric screening shall be
performed in accordance with the standards outlined in Regulations .04 and .05
of this chapter.
(b) The
audiometric screening shall be administered by either:
(i) A physician trained to screen hearing
according to the protocol established in this chapter;
(ii) An audiologist; or
(iii) Appropriately and periodically trained
allied health care staff, under the supervision and monitoring of an
audiologist.
(c) An
audiologist shall determine the facility's training protocol and frequency of
training for allied health care staff. At a minimum, training shall occur at
least once a year.
D. Patients Exempted from Audiometric
Screening. If the patient has a history of hearing impairment as defined in
Regulation .02B(8) of this chapter and documented by an audiologist or
physician, the screening procedure identified in §B and C of this
regulation is not required within the first year after admission.
E. Treatment recommendations related to the
patient's hearing impairment made by either an audiologist, otolaryngologist,
or speech pathologist, shall be incorporated in the patient's Individual
Treatment Plan.
F. Provision and
Maintenance of Hearing Aids.
(1) The patient
and appropriate staff on each shift shall receive, in accordance with a plan
developed by an audiologist, instructions on the care, use, and inspection of
the hearing aid by staff referenced in §C(4)(b)(i) and (ii) of this
regulation or the hearing aid vendor.
(2) Designated staff, as identified in the
Individual Treatment Plan, shall be responsible for ensuring daily monitoring
of hearing aids, and implementing timely repair and immediate replacement of
batteries.
(3) Identification of
the need for replacement as well as the replacement of the patient's hearing
aid shall be documented in the patient's record.
(4) Denial of hearing aid replacement by the
treatment team or the patient's refusal to accept a hearing aid shall be
documented and be reevaluated at a minimum of every 3 months.
(5) The facility shall provide a hearing aid
to the patient when an otolaryngologist or audiologist determines that a
patient would benefit from amplification and related accessories. Payments for
aids shall follow the Administration's policy on payment for medical
devices.