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Medicare Benefit Policy Manual - Chapter 1 PDF
Medicare Benefit Policy Manual - Chapter 1 PDF
Inpatient hospital services are defined in Title XVIII of the Social Security Act (the Act)
and in the regulations (42 CFR 409.10):
A. Subject to the conditions, limitations, and exceptions set forth in this subpart, the term
"inpatient hospital or inpatient CAH services" means the following services furnished to
an inpatient of a participating hospital or of a participating CAH or, in the case of
emergency services or services in foreign hospitals, to an inpatient of a qualified hospital:
B. Inpatient hospital services does not include the following types of services:
Patients covered under hospital insurance are entitled to have payment made on their
behalf for inpatient hospital services. (Inpatient hospital services do not include extended
care services provided by hospitals pursuant to swing bed approvals. See Pub. 100-02,
Chapter 8, §10.3, "Hospital Providers of Extended Care Services."). However, both
inpatient hospital and inpatient SNF benefits are provided under Part A - Hospital
Insurance Benefits for the Aged and Disabled, of Title XVIII).
Additional information concerning the following topics can be found in the following
chapters of this manual:
Blood must be furnished on a day which counts as a day of inpatient hospital services to
be covered as a Part A service and to count toward the blood deductible. Thus, blood is
not covered under Part A and does not count toward the Part A blood deductible when
furnished to an inpatient after the inpatient has exhausted all benefit days in a benefit
period, or where the individual has elected not to use lifetime reserve days. However,
where the patient is discharged on their first day of entitlement or on the hospital's first
day of participation, the hospital is permitted to submit a billing form with no
accommodation charge, but with ancillary charges including blood.
The records for all Medicare hospital inpatient discharges are maintained in CMS for
statistical analysis and use in determining future Prospective Payment System (PPS)
Diagnosis Related Group (DRG) classifications and rates.
Non-PPS hospitals do not pay for noncovered services generally excluded from coverage
in the Medicare Program. This may result in denial of a part of the billed charges or in
denial of the entire admission, depending upon circumstance. In PPS hospitals, the
following are also possible:
1. In appropriately admitted cases where a noncovered procedure was performed,
denied services may result in payment of a different DRG (i.e., one which
excludes payment for the noncovered procedure); or
2. In appropriately admitted cases that become cost outlier cases, denied services
may lead to denial of some or all of an outlier payment.
The following examples illustrate this principle. If care is noncovered because a patient
does not need to be hospitalized, the A/B MAC Part A denies the admission and makes no
Part A (i.e., PPS) payment unless paid under limitation on liability. Under limitation on
liability, Medicare payment may be made when the provider and the beneficiary were
not aware the services were not necessary and could not reasonably be expected to know
that the services were not necessary. For detailed instructions, see Pub. 100-04,
Medicare Claims Processing Manual, Chapter 30,"Limitation on Liability" section 20. If
a patient is appropriately hospitalized but receives (beyond routine services) only
noncovered care, the admission is denied.
NOTE: The A/B MAC Part A does not deny an admission that includes covered care,
even if noncovered care was also rendered. Under PPS, Medicare assumes that it is
paying for only the covered care rendered whenever covered services needed to treat
and/or diagnose the illness were in fact provided.
When the hospital is included in PPS, most of the subsequent discussion regarding
coverage of inpatient hospital services is relevant only in the context of determining the
appropriateness of admissions, which DRG, if any, to pay, and the appropriateness of
payment for any outlier cases.
If a patient receives items or services in excess of, or more expensive than, those for
which payment can be made, payment is made only for the covered items or services or
for only the appropriate prospective payment amount. This provision applies not only to
inpatient services, but also to all hospital services under Parts A and B of the program. If
the items or services were requested by the patient, the hospital may charge him or her
the difference between the amount customarily charged for the services requested and the
amount customarily charged for covered services.
An inpatient is a person who has been admitted to a hospital for bed occupancy for
purposes of receiving inpatient hospital services (see §10.2 below). Generally, a patient
is considered an inpatient if formally admitted as inpatient with the expectation that he or
she will require hospital care that is expected to span at least two midnights and occupy a
bed even though it later develops that the patient can be discharged or transferred to
another hospital and not actually use a hospital bed overnight.
The physician or other practitioner responsible for a patient's care at the hospital is also
responsible for deciding whether the patient should be admitted as an inpatient.
Physicians should use the expectation of the patient to require hospital care that spans at
least two midnights period as a benchmark, i.e., they should order admission for patients
who are expected to require a hospital stay that crosses two midnights and the medical
record supports that reasonable expectation. However, the decision to admit a patient is a
complex medical judgment which can be made only after the physician has considered a
number of factors, including the patient's medical history and current medical needs, the
types of facilities available to inpatients and to outpatients, the hospital's by-laws and
admissions policies, and the relative appropriateness of treatment in each setting. Factors
to be considered when making the decision to admit include such things as:
• The need for diagnostic studies that appropriately are outpatient services (i.e.,
their performance does not ordinarily require the patient to remain at the hospital
for 24 hours or more) to assist in assessing whether the patient should be
admitted; and
• The availability of diagnostic procedures at the time when and at the location
where the patient presents.
Admissions of particular patients are not covered or noncovered solely on the basis of the
length of time the patient actually spends in the hospital. In certain specific situations
coverage of services on an inpatient or outpatient basis is determined by the following
rules:
Minor Surgery or Other Treatment - When patients with known diagnoses enter a
hospital for a specific minor surgical procedure or other treatment that is expected to keep
them in the hospital for only a few hours (less than 24), they are considered outpatients
for coverage purposes regardless of: the hour they came to the hospital, whether they
used a bed, and whether they remained in the hospital past midnight.
Renal Dialysis - Renal dialysis treatments are usually covered only as outpatient services
but may under certain circumstances be covered as inpatient services depending on the
patient's condition. Patients staying at home, who are ambulatory, whose conditions are
stable and who come to the hospital for routine chronic dialysis treatments, and not for a
diagnostic workup or a change in therapy, are considered outpatients. On the other hand,
patients undergoing short-term dialysis until their kidneys recover from an acute illness
(acute dialysis), or persons with borderline renal failure who develop acute renal failure
every time they have an illness and require dialysis (episodic dialysis) are usually
inpatients. A patient may begin dialysis as an inpatient and then progress to an outpatient
status.
Under original Medicare, the Quality Improvement Organization (QIO), for each hospital
is responsible for deciding, during review of inpatient admissions on a case-by-case basis,
whether the admission was medically necessary. Medicare law authorizes the QIO to
make these judgments, and the judgments are binding for purposes of Medicare coverage.
In making these judgments, however, QIOs consider only the medical evidence which
was available to the physician at the time an admission decision had to be made. They do
not take into account other information (e.g., test results) which became available only
after admission, except in cases where considering the post-admission information would
support a finding that an admission was medically necessary.
NOTE: When patients requiring extended care services are admitted to beds in a
hospital, they are considered inpatients of the hospital. In such cases, the services
furnished in the hospital will not be considered extended care services, and payment may
not be made under the program for such services unless the services are extended care
services furnished pursuant to a swing bed agreement granted to the hospital by the
Secretary of Health and Human Services.
The program will pay the same amount for routine accommodations services whether the
patient has a private room not medically necessary, a private room medically necessary
(Medicare does not pay for deluxe accommodations in any case), a semiprivate room (2-,
3-, or 4-bed accommodations), or ward accommodations, if its ward accommodations are
consistent with program purposes (see §10.1.6 below).
• The patient (or relative or other person acting on their behalf) has requested the
private room, and the provider informs them of the amount of charge at the time
of the request.
The private room differential may not exceed the difference between the customary
charge for the accommodations furnished and the most prevalent semiprivate
accommodation rate at the time of the patient's admission.
Where the provider bills for a private room as a covered service, i.e., shows the charge
for the room as a covered charge on the Form CMS-1450, the A/B MAC (A) will deem
the private room to be medically necessary. Where the provider, on the other hand,
shows a private differential as a noncovered charge, the A/B MAC (A) will assume that
the private room is not medically necessary.
If the beneficiary (or their representative) protests a charge for the private room on the
grounds that the privacy was medically necessary, such protest will, if not in written
form, be reduced to writing and forwarded to the A/B MAC (A). The A/B MAC (A) will
then develop the facts and make a specific determination regarding the medical necessity
of the private room. (If an A/B MAC (A) receives many protests of this kind, the
provider may need guidance on what constitutes medical necessity for privacy). If the
protest is received after the claim is processed, it will be treated as a request for
reconsideration.
If at any time in the course of development (or thereafter within the period when the
determination is not administratively final), the provider acknowledges that the private
room was medically necessary; the A/B MAC (A) will make an immediate finding to this
effect.
Where it is necessary to develop the medical necessity of a private room, the guidelines
in subsections §§10.1.2 and 10.1.3 below will apply.
In establishing the medical necessity for isolation, the date of the physician's written
statement is not controlling, nor is the presence of a written statement. The crucial
question is whether a private room was ordered by the physician because it is necessary
for the health of the patient himself or herself or of other patients. In the absence of such
an order, a patient who requested the room with knowledge of the amount of the charge
may be charged appropriately, even though a physician subsequently submits a statement
that the room was medically necessary. There may be cases in which the physician's
written statement of medical necessity, though dated after admission or even after
discharge, merely confirms an order made informally at or before the time the beneficiary
was admitted to the private room (e.g., the physician made arrangements by phone for the
patient's admission, gave the diagnosis, and stated the beneficiary would need a private
room). In such cases, assuming that the private room was medically necessary, the lack
of a written statement by the physician, or the fact that the written statement was prepared
after discharge, would not be controlling. The patient may not be charged.
Beneficiaries found to need a private room (either because they need isolation for
medical reasons or because they need immediate admission when no other
accommodations are available) may be assigned to any of the provider's private rooms.
They do not have the right to insist on the private room of their choice, but their
preferences should be given the same consideration as if they were paying all provider
charges themselves. The program does not, under any circumstances, pay for personal
comfort items. Thus, the program does not pay for deluxe accommodations and/or
services. These would include a suite, or a room substantially more spacious than is
required for treatment, or specially equipped or decorated, or serviced for the comfort and
convenience of persons willing to pay a differential for such amenities. If the beneficiary
(or representative) requests such deluxe accommodations, the provider should advise that
there will be a charge, not covered by Medicare, of a specified amount per day (not
exceeding the differential defined in the next sentence); and may charge the beneficiary
that amount for each day he/she occupies the deluxe accommodations. The maximum
amount the provider may charge the beneficiary for such accommodations is the
differential between the most prevalent private room rate at the time of admission and the
customary charge for the room occupied. Beneficiaries may not be charged this
differential if they (or their representative) do not request the deluxe accommodations.
The beneficiary may not be charged such a differential in private room rates if that
differential is based on factors other than personal comfort items. Such factors might
include differences between older and newer wings, proximity to lounge, elevators or
nursing stations, desirable view, etc. Such rooms are standard 1-bed units and not deluxe
rooms for purposes of these instructions, even though the provider may call them deluxe
and have a higher customary charge for them. No additional charge may be imposed
upon the beneficiary who is assigned to a room that may be somewhat more desirable
because of these factors.
If the patient is admitted to a provider which has only private accommodations, and no
semiprivate or ward accommodations, medical necessity will be deemed to exist for the
accommodations furnished. Beneficiaries may not be subjected to an extra charge for a
private room in an all-private room provider.
10.1.6 - Wards
(Rev. 1, 10-01-03)
A3-3101.1.F, HO-210.1.F
The law contemplates that Medicare patients should not be assigned to ward
accommodations except at the patient's request or for a reason consistent with the
purposes of the health insurance program.
When ward accommodations are furnished at the patient's request or for a reason
determined to be consistent with the program's purposes, payment will be based on the
average per diem cost of routine services (see §10.1.1 above). Where ward
accommodations are assigned for other reasons, the law provides what may be a
substantial penalty. (See §10.1.6.2 below).
Any request by the patient (or relative or other person responsible for his or her affairs)
for ward accommodations must be obtained by the provider in writing and kept in its
files.
10.1.6.1 - Assignment Consistent With Program Purposes
(Rev. 1, 10-01-03)
A3-3101.1.F.1, HO-210.1.F.1
It is considered to be consistent with the program's purposes to assign the patient to ward
accommodations if all semiprivate accommodations are occupied, or the facility has no
semiprivate accommodations. However, the patient must be moved to semiprivate
accommodations if they become available during the stay.
Some hospitals have a policy of placing in wards all patients who do not have private
physicians. Such a practice may be consistent with the purposes of the program if the
A/B MAC (A) determines that the ward assignment inures to the benefit of the patient.
In making this determination, the principal consideration is whether the assignment is
likely to result in better medical treatment of the patient (e.g., it facilitates necessary
medical and nursing supervision and treatment). The A/B MAC (A) should ask a
provider having this policy to submit a statement describing how the assignments are
made, their purpose, and the effect on the care of patients so assigned.
If the A/B MAC (A) makes a favorable determination on a practice affecting all ward
assignments of Medicare patients in the institution, a reference should be made on the
appropriate billing form for patients to whom the hospital assigned a ward pursuant to
such practice.
It is not consistent with the purposes of the law to assign a patient ward accommodation
based on their social or economic status, their national origin, race, or religion, or their
entitlement to benefits as a Medicare patient, or any other such discriminatory reason. It
is also inconsistent with the purposes of the law to assign patients to ward
accommodations merely for the convenience or financial advantage of the institution.
Additionally, under DRGs, there no longer is a reduction to payment or an adjustment to
the end of year settlement.
10.1.7 - Charges
(Rev. 1, 10-01-03)
A3-3101.1.G, HO-210.1.G
Customary charges means amounts which the hospital or skilled nursing facility is
uniformly charging patients currently for specific services and accommodations. The
most prevalent rate or charge is the rate that applies to the greatest number of semiprivate
or private beds in the institution.
The following guidance applies to all inpatient hospital and CAH services unless
otherwise specified. For the remainder of this guidance, references to hospitals includes
CAHs. The complete requirements for the physician certification are found in 42 CFR
Part 424 subpart B, and requirements for admission orders are found at 42 CFR 412.3.
a. Reason for inpatient services: The physician certifies the reasons for
either— (i) Continued hospitalization of the patient for inpatient medical
treatment or medically required inpatient diagnostic study; or (ii) Special
or unusual services for outlier cases under the applicable prospective
payment system for inpatient services. For example, documentation of an
admitting diagnosis could fulfill this part of the certification requirement.
b. The estimated (or actual) time the beneficiary requires or required in the
hospital: The physician certifies the estimated time in the hospital the
beneficiary requires (if the certification is completed prior to discharge)
or the actual time in the hospital (if the certification is completed at
discharge). Estimated or actual length of stay is most commonly reflected
in the progress notes where the practitioner discusses the assessment and
plan. For the purposes of meeting the requirement for certification,
expected or actual length of stay may be documented in the order or a
separate certification or recertification form, but it is also acceptable if
discussed in the progress notes assessment and plan or as part of routine
discharge planning.
If the reason an inpatient is still in the hospital is that they are waiting for
availability of a skilled nursing facility (SNF) bed, the regulations at 42
CFR 424.13(c) and 424.14(e) provide that a beneficiary who is already
appropriately an inpatient can be kept in the hospital as an inpatient if the
only reason they remain in the hospital is they are waiting for a post-acute
SNF bed. The physician may certify the need for continued inpatient
admission on this basis.
d. For inpatient CAH services only, the physician must certify that the
beneficiary may reasonably be expected to be discharged or transferred to
a hospital within 96 hours after admission to the CAH.
Time as an outpatient at the CAH does not count towards the 96 hour
certification requirement. The clock for the 96 hour certification
requirement only begins once the individual is admitted to the CAH as an
inpatient. Time in a CAH swing-bed also does not count towards the 96
hour certification requirement.
1. Content: The ordering practitioner’s order contains the instruction that the
beneficiary should be formally admitted for hospital inpatient care. The order
must specify admission for inpatient services. Inpatient rehabilitation
facilities (IRFs) must adhere to the admission requirements specified in 42
CFR 412.622. The two midnight benchmark does not apply in IRFs.
4. Timing: The order must be furnished at or before the time of the inpatient
admission. The order can be written in advance of the formal admission (e.g.,
for a pre‐scheduled surgery), but the inpatient admission does not occur until
hospital care services are provided to the beneficiary. Conversely, in the
unusual case in which a patient is admitted as an inpatient prior to an order
to admit and there is no documented verbal order, the inpatient stay should
not be considered to commence until the inpatient admission order is
documented. CMS does not permit retroactive orders. Authentication by the
ordering practitioner of the order (either by signature or, in the case of an
initial order under (B)(2)(a) or a verbal order under (B)(2)(b),
countersignature) is required prior to discharge for all inpatient cases.
Nursing and other related services, use of hospital facilities, and medical social services
ordinarily furnished by the hospital for the care and treatment of inpatients are covered
under hospital insurance and included in the Prospective Payment system payment.
NOTE: The services of a private-duty nurse or other private-duty attendant are not
covered. Private-duty nurses or private-duty attendants are registered nurses, licensed
practical nurses, or any other trained attendant whose services ordinarily are rendered to,
and restricted to, a particular patient by arrangement between the patient and the private-
duty nurse or attendant. Such persons are engaged or paid by an individual patient or by
someone acting on their behalf, including a hospital that initially incurs the costs and
looks to the patient for reimbursement for such noncovered services.
Where the hospital acts on behalf of a patient, the services of the private-duty nurse or
other attendant under such an arrangement are not inpatient hospital services regardless
of the control which the hospital may exercise with respect to the services rendered by
such private-duty nurse or attendant.
Medical social services are services which contribute meaningfully to the treatment of a
patient's condition. Such services include, but are not limited to:
• Assessment of the social and emotional factors related to the patient's illness, need
for care, response to treatment, and adjustment to care in the facility;
• Appropriate action to obtain case work services to assist in resolving problems in
these areas; and
Drugs and biologicals for use in the hospital, which are ordinarily furnished by the
hospital for the care and treatment of inpatients, are covered.
Three basic requirements must be met for a drug or biological furnished by a hospital to
be a covered hospital service:
2. The drug or biological must meet the statutory definition. Under the statute,
payment may be made for a drug or biological only where it is included, or
approved for inclusion, in the latest official edition of the United States
Pharmacopoeia-National Formulary (USP-NF), the United States Pharmacopoeia
Drug Information (USP DI), or the American Dental Association (ADA) Guide to
Dental Therapeutics, except for those drugs and biologicals unfavorably evaluated
in the ADA Guide to Dental Therapeutics. Combination drugs are also included
in the definition of drugs if the combination itself or all of the therapeutic
ingredients of the combination are included, or approved for inclusion, in any of
the above drug compendia. Drugs and biologicals are considered approved for
inclusion in a compendium if approved under the established procedure by the
professional organization responsible for revision of the compendium; or be
approved by the pharmacy and drug therapeutics or equivalent committee of the
medical staff of the hospital for use in the hospital; and
3. Use of the drug or biological must be safe and effective and otherwise reasonable
and necessary as specified in the Medicare Benefit Policy Manual, Chapter 15,
“Covered Medical and Other Health Services,” §50.
Drugs and biologicals, which have not received final marketing approval by the FDA, are
not covered unless CMS instructs the A/B MAC (A) to the contrary. However, FDA-
approved drugs are used for indications other than those specified on the labeling. As
long as the FDA has not specified such use as nonapproved, coverage is determined
taking into consideration the generally accepted medical practice in the community. For
example, the labeling of certain chemotherapeutic drugs indicates their use in the therapy
of specified types of cancer. However, based on experience and empirical evidence,
physicians may prescribe these drugs for a wider range of cancer treatments than what is
indicated in the labeling. Local medical review policy may or may not grant coverage,
depending on the circumstances.
A hospital stay solely for the purpose of use of a drug or biological that is determined not
reasonable and necessary is not covered.
Medicare covers only those drugs and biologicals included, or approved for inclusion, in
the latest official edition or revision of the compendia as previously listed.
Where a drug is excluded from coverage because it is unfavorably evaluated in either the
AMA Drug Evaluations or Accepted Dental Therapeutics, the exclusion applies to all
uses for which the drug or biological was so unfavorably evaluated.
Drugs and biologicals are considered approved for use in the hospital if selected for
inclusion in the hospital drug list of formulary under the procedure of the committee
established for that purpose. Express approval is required; the fact that a drug or
biological has not been specifically determined to be unacceptable for use in the hospital
does not constitute approval.
Drugs and biologicals are covered if approved for general use in the hospital, or if
approved for use by a particular patient or group of patients. Approval by a pharmacy
and drug therapeutics committee is an alternative to approval for inclusion of the drug or
biological in an approved drug compendium (see §30.1 above); such approval does not
preclude the need for a determination of medical necessity. An investigational drug is
not considered to meet the reasonable and necessary test since its efficacy has not yet
been established.
The decision of individual hospitals should not transcend the determinations of the Food
and Drug Administration and Public Health Service in respect to the safety and
effectiveness of drugs. Therefore, even if approved by an appropriate hospital
committee, the reasonable cost of an investigational or other nonapproved drug or
biological (e.g., Laetrile) cannot be reimbursed. This exclusion from payment applies
whether or not the drug or biological is administered during the course of an otherwise
covered hospital stay, since payment may not be made for items and services that are not
reasonable and necessary. A hospital stay solely for the purpose of administering a drug
or biological that is not reasonable and necessary, including an investigational drug or
biological, is not covered and the drug or biological itself is not covered.
Combination drugs are covered if the combination itself or all of the therapeutic
ingredients of the combination are included, or approved for inclusion, in any of the
designated drug compendia. Any combination drug approved for use in the hospital by
the pharmacy and drug therapeutics or equivalent committee is covered.
Drugs and biologicals not included in the drug list or formulary maintained by the
hospital's pharmacy and drug therapeutics committee may be covered if the hospital has a
policy which permits such drugs to be furnished to a patient at the special request of a
physician. However, in order to be covered, such drugs and biologicals must be included,
or approved for inclusion, in one of the designated drug compendia. (In addition, a
combination drug, or all of its therapeutic ingredients, would have to be included or
approved for inclusion in one of the compendia.)
Drugs and biologicals furnished by a hospital to an inpatient for use outside the hospital
are, in general, not covered as inpatient hospital services. However, if the drug or
biological is deemed medically necessary to permit or facilitate the patient's departure
from the hospital, and a limited supply is required until the patient can obtain a
continuing supply, the limited supply of the drug or biological is covered as an inpatient
hospital service.
Supplies, appliances, and equipment, which are ordinarily furnished by the hospital for
the care and treatment of the beneficiary solely during the inpatient hospital stay, are
covered inpatient hospital services.
Under certain circumstances, supplies, appliances, and equipment used during the
beneficiary's inpatient stay are covered under Part A even though the supplies, appliances
and equipment leave the hospital with the patient upon discharge. These are
circumstances in which it would be unreasonable or impossible from a medical
standpoint to limit the patient's use of the item to the periods during which the individual
is an inpatient. Examples of items covered under this rule are:
• Items which are temporarily installed in or attached to the patient's body while an
inpatient, and which are also necessary to permit or facilitate the patient's release
from the hospital, such as tracheotomy or drainage tubes.
Hospital “admission packs” containing primarily toilet articles, such as soap,
toothbrushes, toothpaste, and combs, are covered under Part A if routinely furnished by
the hospital to all its inpatients. If not routinely furnished to all patients, the packs are not
covered. In that situation, the hospital may charge beneficiaries for the pack, but only if
they request it with knowledge of what they are requesting and what the charge to them
will be.
Supplies, appliances, and equipment furnished to an inpatient for use only outside the
hospital are not, in general, covered as inpatient hospital services. However, a temporary
or disposable item, which is medically necessary to permit or facilitate the patient's
departure from the hospital and is required until the patient can obtain a continuing
supply, is covered as an inpatient hospital service.
Such services to hospital inpatients may be covered under Part A even when furnished off
the hospital premises. For example, diagnostic or therapeutic services of an audiologist
off the hospital premises are covered if billed for by the hospital under arrangements (see
Pub 100-01, the Medicare General Information, Eligibility, and Entitlement Manual,
Chapter 5, §10.3, for further information concerning “under arrangements”), if the
services are furnished at a speech and hearing center, and if the audiologist meets the
qualifications for an audiologist:
• Surgical dressings, and splints, casts, and other devices used for the reduction of
fractures and dislocations;
• Prosthetic devices (other than dental) which replace all or part of an internal body
organ (including contiguous tissue) or replace all or part of the function of a
permanently inoperative or malfunctioning internal body organ; and
• Leg, arm, back, and neck braces, trusses, and artificial legs, arms, and eyes.
With respect to items that leave the hospital with the patient upon discharge, such as
splints or casts, the rules for determining whether the item is covered are the same as the
rules set forth above for supplies, appliances, and equipment.
A consulting physician is one whose services include history taking, examination of the
patient and, in each case, furnishing to the attending physician an opinion regarding
diagnosis or treatment. A physician providing clinical laboratory services for patients of
other physicians is not considered to be a consulting physician.
A laboratory operated by or under the supervision of a hospital (or the organized medical
staff of the hospital) that does not meet at least the definition of an emergency hospital is
considered to be an independent laboratory. However, a laboratory serving hospital
patients and operated on the premises of a hospital that meets the definition of an
emergency hospital is presumed to be subject to the supervision of the hospital or its
organized medical staff and is not an independent laboratory. A laboratory that a
physician or group of physicians maintains for performing diagnostic tests in connection
with their own or the group practice is also not considered to be an independent
laboratory.
The "Conditions of Participation for Hospitals (HIRM-1)" call for independent clinical
laboratory services furnished under arrangements made by a hospital to be furnished only
by a laboratory meeting the specified conditions for coverage under the program. These
require that:
• Where State or applicable local law provides for licensing of independent clinical
laboratories, the laboratory is either licensed under law or is approved as meeting
the requirements for licensing by the State or local agency responsible for
licensing laboratories; and
• Such laboratories also meet the health and safety requirements prescribed by the
Secretary of Health and Human Services. (See “The Conditions of Participation
for Hospitals” at 42 CFR 482).
Diagnostic services furnished a hospital inpatient under arrangements with the laboratory
of another participating hospital are reimbursable on a cost basis under Part A to the
hospital obtaining the services if the hospital is PPS exempt. If the hospital is not
exempt, there is not separate payment for lab services furnished to inpatients.
NOTE: Where a PPS exempt hospital obtains diagnostic laboratory services for
inpatients under arrangements described in §§50.3 and 50.4 the cost to the hospital
obtaining the services would be the reasonable charge for the laboratory's service.
Hospital insurance covers the reasonable cost of the services of medical or osteopathic
interns or residents-in-training under a teaching program approved by the appropriate
approving body.
The services of interns and residents-in-training in the field of podiatry who are in a
residency program approved by the Council on Podiatric Medical Education of the
American Podiatric Medical Association are covered on the same basis as the services of
other interns and residents in other approved residency programs.
When the hospital services are covered, all ancillary services such as x-rays,
administration of anesthesia, use of the operating room, etc., are covered.
Regardless of whether the inpatient hospital services are covered, the medical services of
physicians furnished in connection with noncovered dental services are not covered. The
services of an anesthesiologist, radiologist, or pathologist whose services are performed
in connection with the care, treatment, filling, removal, or replacement of teeth or
structures directly supporting teeth are not covered.
Reasonable and necessary services associated with pregnancy are covered and
reimbursable under the Medicare program. Because pregnancy is a condition sufficiently
at variance with the usual state of health, it is appropriate for a pregnant woman to seek
medical care. The increased possibility of illness or injury accompanying this condition
is well recognized, and medical supervision is required throughout pregnancy and for a
brief period beyond. Skilled medical management is appropriate throughout the events of
pregnancy, beginning with diagnosis of the condition, continuing through delivery, and
ending after the necessary postnatal care. Similarly, if the pregnancy terminates, whether
spontaneously or for therapeutic reasons (i.e., where the life of the mother would be
endangered if the fetus were brought to term), the need for skilled medical management
and/or medical services is equally as important as in those cases carried to full term.
After the infant is delivered, items and services furnished to the infant cannot be covered
and reimbursed under the program on the basis of the mother's eligibility.
90 - Termination of Pregnancy
(Rev. 1, 10-01-03)
B3-4276.1,.2
Effective for services furnished on or after October 1, 1998, Medicare will cover
abortions procedures in the following situations:
2. In the case where a woman suffers from a physical disorder, physical injury, or
physical illness, including a life-endangering physical condition caused by the
pregnancy itself that would, as certified by a physician, place the woman in
danger of death unless an abortion is performed.
NOTE: The "G7" modifier must be used with the following CPT codes in order for
these services to be covered when the pregnancy resulted from rape or incest, or the
pregnancy is certified by a physician as life threatening to the mother:
Effective for services rendered on or after January 15, 1980, reasonable and necessary
services associated with treatment for infertility are covered under Medicare. Like
pregnancy (see §80 above), infertility is a condition sufficiently at variance with the usual
state of health to make it appropriate for a person who normally would be expected to be
fertile to seek medical consultation and treatment. A/B MACs (A) should coordinate
with QIOs to see that utilization guidelines are established for this treatment if
inappropriate utilization or abuse is suspected.
The IRF benefit is not to be used as an alternative to completion of the full course of
treatment in the referring hospital. A patient who has not yet completed the full course of
treatment in the referring hospital is expected to remain in the referring hospital, with
appropriate rehabilitative treatment provided, until such time as the patient has completed
the full course of treatment. Though medical management can be performed in an IRF,
patients must be able to fully participate in and benefit from the intensive rehabilitation
therapy program provided in IRFs in order to be transferred to an IRF. IRF admissions
for patients who are still completing their course of treatment in the referring hospital and
who therefore are not able to participate in and benefit from the intensive rehabilitation
therapy services provided in IRFs will not be considered reasonable and necessary.
Conversely, the IRF benefit is not appropriate for patients who have completed their full
course of treatment in the referring hospital, but do not require intensive rehabilitation.
Medicare benefits are available for such patients in a less-intensive setting.
A/B MACs (A) must consider the documentation contained in a patient’s IRF medical
record when determining whether an IRF admission was reasonable and necessary,
specifically focusing on the preadmission screening, the post-admission physician
evaluation, the overall plan of care, and the admission orders.
The preadmission screening documentation must indicate the patient’s prior level of
function (prior to the event or condition that led to the patient’s need for intensive
rehabilitation therapy), expected level of improvement, and the expected length of time
necessary to achieve that level of improvement. It must also include an evaluation of the
patient’s risk for clinical complications, the conditions that caused the need for
rehabilitation, the treatments needed (i.e., physical therapy, occupational therapy, speech-
language pathology, or prosthetics/orthotics), expected frequency and duration of
treatment in the IRF, anticipated discharge destination, any anticipated post-discharge
treatments, and other information relevant to the care needs of the patient.
If the patient is being transferred from a referring hospital, the preadmission screening
may be done in person or through a review of the patient’s medical records from the
referring hospital (either paper or electronic format), as long as those medical records
contain the necessary assessments to make a reasonable determination. However, a
preadmission screening conducted entirely by telephone will not be accepted without
transmission of the patient’s medical records from the referring hospital to the IRF and a
review of those records by licensed or certified clinical staff in the IRF.
The IRF is responsible for developing a thorough preadmission screening process for
patients admitted to the IRF from the home or community-based environment, which is
expected to include all of the required elements described in this section. However, such
admissions may not necessarily involve the use of medical records from a prior hospital
stay in another inpatient hospital setting unless such records are pertinent to the
individual patient’s situation.
The “rehabilitation physician” need not be a salaried employee of the IRF but must be a
licensed physician with specialized training and experience in rehabilitation. For ease of
exposition throughout this document, this physician will be referred to as a “rehabilitation
physician”.
In order for the IRF stay to be considered reasonable and necessary, the post-admission
physician evaluation must be completed within the first 24 hours of admission to the IRF
and must support the medical necessity of the IRF admission. The post-admission
physician evaluation documentation must be retained in the patient’s medical record at
the IRF.
What to do if there are differences between the preadmission screening and the post-
admission physician evaluation (within the first 24 hours of admission to the IRF):
In most cases, the clinical picture of the patient that emerges from the post-admission
physician evaluation will closely resemble the information documented in the
preadmission screening. However, for a variety of reasons, the patient’s condition at the
time of admission may occasionally not match the description of the patient’s condition
on the preadmission screening. This could occur, for example, if the patient’s condition
changes after the preadmission screening is completed. In these cases, it is important for
a rehabilitation physician to note the discrepancy and to document any deviations from
the preadmission screening as a result. For example, if the patient’s preadmission
screening indicated an expectation that the patient would actively participate in an
intensive rehabilitation therapy program on admission to the IRF, but the patient is only
able to tolerate a less intensive therapy program on the first day due to an increase in pain
secondary to a long ambulance trip to the IRF, the IRF does not have to discharge the
patient since the clinicians fully expect the patient to be able to participate in the
intensive rehabilitation program the next day. Instead, the reason for the temporary
change must be noted in the patient’s medical record at the IRF.
In addition, the preadmission screening and the post-admission physician evaluation
could differ in rare cases when a patient’s preadmission screening indicates that the
patient is an appropriate candidate for IRF care but this turns out not to be the case,
either, for example, due to a marked improvement in the patient’s functional ability since
the time of the preadmission screening or an inability to meet the demands of the IRF
rehabilitation program. If this occurs, the IRF must immediately begin the process of
discharging the patient to another setting of care. It might take a day or more for the IRF
to find placement for the patient in another setting of care. A/B MACs (A) will therefore
allow the patient to continue to receive treatment in the IRF until placement in another
setting can be found. However, in these particular cases, any IRF services provided after
the 3rd day following the patient’s admission to the IRF (considering the day of admission
to be the 1st day) are not considered reasonable and necessary. In these particular cases,
instead of denying the entire IRF claim for not meeting the criteria in section 110.2 of
this chapter, Medicare authorizes its A/B MACs (A) to permit the IRF claim to be paid at
the appropriate case mix group (CMG) for IRF patient stays of 3 days or less.
Whereas the individual assessments of appropriate clinical staff will contribute to the
information contained in the overall plan of care, it is the sole responsibility of a
rehabilitation physician to integrate the information that is required in the overall plan of
care and to document it in the patient’s medical record at the IRF.
In the unlikely event that the patient’s actual length of stay and/or the expected intensity,
frequency, and duration of physical, occupational, speech-language pathology, and
prosthetic/orthotic therapies in the IRF differ significantly from the expectations
indicated in the overall plan of care, then the reasons for the discrepancies must be
documented in detail in the patient’s medical record at the IRF.
In order for the IRF admission to be considered reasonable and necessary, the overall
plan of care must be completed within the first 4 days of the IRF admission; it must
support the determination that the IRF admission is reasonable and necessary; and it must
be retained in the patient’s medical record at the IRF.
While CMS believes that it may be good practice to conduct the first interdisciplinary
team meeting within the first 4 days of admission to develop the overall individualized
plan of care, CMS believes that there may be other ways of developing the overall
individualized plan of care. Thus, IRFs may develop this required documentation using
whatever internal processes they believe are most appropriate.
At the time that each Medicare Part A fee-for-service patient is admitted to an IRF, a
physician must generate admission orders for the patient's care. These admission orders
must be retained in the patient’s medical record at the IRF.
Medicare now requires that the IRF patient assessment instrument (IRF-PAI) forms be
included in the patient’s medical record at the IRF (either in electronic or paper format).
The information in the IRF-PAIs must correspond with all of the information provided in
the patient’s IRF medical record.
In order for IRF care to be considered reasonable and necessary, the documentation in the
patient’s IRF medical record (which must include the preadmission screening described
in section 110.1.1, the post-admission physician evaluation described in section 110.1.2,
the overall plan of care described in section 110.1.3, and the admission orders described
in section 110.1.4) must demonstrate a reasonable expectation that the following criteria
were met at the time of admission to the IRF:
1. The patient must require the active and ongoing therapeutic intervention of multiple
therapy disciplines (physical therapy, occupational therapy, speech-language
pathology, or prosthetics/orthotics), one of which must be physical or occupational
therapy.
3. The patient must reasonably be expected to actively participate in, and benefit
significantly from, the intensive rehabilitation therapy program that is defined in
section 110.2.2 at the time of admission to the IRF. The patient can only be expected
to benefit significantly from the intensive rehabilitation therapy program if the
patient’s condition and functional status are such that the patient can reasonably be
expected to make measurable improvement (that will be of practical value to improve
the patient’s functional capacity or adaptation to impairments) as a result of the
rehabilitation treatment, as defined in section 110.3, and if such improvement can be
expected to be made within a prescribed period of time. The patient need not be
expected to achieve complete independence in the domain of self-care nor be
expected to return to his or her prior level of functioning in order to meet this
standard.
A primary distinction between the IRF environment and other rehabilitation settings is
the interdisciplinary approach to providing rehabilitation therapy services in an IRF.
Patients requiring only one discipline of therapy would not need this interdisciplinary
approach to care. For this reason, the information in the patient’s IRF medical record
(especially the required documentation described in section 110.1) must document a
reasonable expectation that, at the time of admission to the IRF, the patient required the
active and ongoing therapeutic intervention of multiple therapy disciplines (physical
therapy, occupational therapy, speech-language pathology, or prosthetics/orthotics), one
of which must be physical or occupational therapy.
A primary distinction between the IRF environment and other rehabilitation settings is
the intensity of rehabilitation therapy services provided in an IRF. For this reason, the
information in the patient’s IRF medical record (especially the required documentation
described in section 110.1) must document a reasonable expectation that at the time of
admission to the IRF the patient generally required the intensive rehabilitation therapy
services that are uniquely provided in IRFs. Although the intensity of rehabilitation
services can be reflected in various ways, the generally-accepted standard by which the
intensity of these services is typically demonstrated in IRFs is by the provision of
intensive therapies at least 3 hours per day at least 5 days per week. However, this is not
the only way that such intensity of services can be demonstrated (that is, CMS does not
intend for this measure to be used as a “rule of thumb” for determining whether a
particular IRF claim is reasonable and necessary).
The intensity of therapy services provided in IRFs could also be demonstrated by the
provision of 15 hours of therapy per week (that is, in a 7-consecutive day period starting
from the date of admission). For example, if a hypothetical IRF patient was admitted to
an IRF for a hip fracture, but was also undergoing chemotherapy for an unrelated issue,
the patient might not be able to tolerate therapy on a predictable basis due to the
chemotherapy. Thus, this hypothetical patient might be more effectively served by the
provision of 4 hours of therapy 3 days per week and 1 ½ hours of therapy on 2 (or more)
other days per week in order to accommodate his or her chemotherapy schedule. Thus,
IRFs may also demonstrate a patient’s need for intensive rehabilitation therapy services
by showing that the patient required and could reasonably be expected to benefit from at
least 15 hours of therapy per week (defined as a 7-consecutve day period starting from
the date of admission), as long as the reasons for the patient’s need for this program of
intensive rehabilitation are well-documented in the patient’s IRF medical record and the
overall amount of therapy can reasonably be expected to benefit the patient. Many IRF
patients will medically benefit from more than 3 hours of therapy per day or more than 15
hours of therapy per week, when all types of therapy are considered. However, the
intensity of therapy provided must be reasonable and necessary under section
1862(a)(1)(A) of the Act and must never exceed the patient’s level of need or tolerance,
or compromise the patient’s safety. See below for a brief exceptions policy for
temporary and unexpected events.
The required therapy treatments must begin within 36 hours from midnight of the day of
admission to the IRF. Therapy evaluations constitute the beginning of the required
therapy services. As such, they are included in the total daily/weekly provision of
therapies used to demonstrate the intensity of therapy services provided in an IRF.
The standard of care for IRF patients is individualized (i.e., one-on-one) therapy. Group
therapies serve as an adjunct to individual therapies. In those instances in which group
therapy better meets the patient’s needs on a limited basis, the situation/rationale that
justifies group therapy should be specified in the patient’s medical record at the IRF.
Brief Exceptions Policy - While patients requiring an IRF stay are expected to need and
receive an intensive rehabilitation therapy program, as described above, this may not be
true for a limited number of days during a patient’s IRF stay because patients’ needs vary
over time. For example, if an unexpected clinical event occurs during the course of a
patient’s IRF stay that limits the patient’s ability to participate in the intensive therapy
program for a brief period not to exceed 3 consecutive days (e.g., extensive diagnostic
tests off premises, prolonged intravenous infusion of chemotherapy or blood products,
bed rest due to signs of deep vein thrombosis, exhaustion due to recent ambulance
transportation, surgical procedure, etc.), the specific reasons for the break in the provision
of therapy services must be documented in the patient’s IRF medical record. If these
reasons are appropriately documented in the patient’s IRF medical record, such a break in
service (of limited duration) will not affect the determination of the medical necessity of
the IRF admission. Thus, A/B MACs (A) may approve brief exceptions to the intensity
of therapy requirement in these particular cases if they determine that the initial
expectation of the patient’s active participation in intensive therapy during the IRF stay
was based on a diligent preadmission screening, post-admission physician evaluation, and
overall plan of care that were based on reasonable conclusions.
The information in the patient’s IRF medical record (especially the required
documentation described in section 110.1) must document a reasonable expectation that
at the time of admission to the IRF the patient’s condition is such that the patient can
reasonably be expected to actively participate in, and significantly benefit from, the
intensive rehabilitation therapy program that is defined in section 110.2.2.
A primary distinction between the IRF environment and other rehabilitation settings is
the high level of physician supervision that accompanies the provision of intensive
rehabilitation therapy services. For this reason, the information in the patient’s IRF
medical record (especially the required documentation described in section 110.1) must
document a reasonable expectation that at the time of admission to the IRF the patient’s
medical management and rehabilitation needs require an inpatient stay and close
physician involvement. Close physician involvement in the patient’s care is
demonstrated by documented face-to-face visits from a rehabilitation physician or other
licensed treating physician with specialized training and experience in rehabilitation at
least 3 days per week throughout the patient’s IRF stay. The purpose of the face-to-face
visits is to assess the patient both medically and functionally (with an emphasis on the
important interactions between the patient’s medical and functional goals and progress),
as well as to modify the course of treatment as needed to maximize the patient’s capacity
to benefit from the rehabilitation process. Other physician specialties may treat and visit
the patient, as needed, more often than 3 days per week. However, the requirement for
IRF physician supervision is intended to ensure that IRF patients receive more
comprehensive assessments of their functional goals and progress, in light of their
medical conditions, by a rehabilitation physician with the necessary training and
experience to make these assessments at least 3 times per week. The required
rehabilitation physician visits must be documented in the patient’s medical record at the
IRF.
An IRF stay will only be considered reasonable and necessary if at the time of admission
to the IRF the documentation in the patient’s IRF medical record indicates a reasonable
expectation that the complexity of the patient’s nursing, medical management, and
rehabilitation needs requires an inpatient stay and an interdisciplinary team approach to
the delivery of rehabilitation care. That is, the complexity of the patient’s condition must
be such that the rehabilitation goals indicated in the preadmission screening, the post-
admission physician evaluation, and the overall plan of care can only be achieved through
periodic team conferences—at least once a week—of an interdisciplinary team of
medical professionals (as defined below).
Interdisciplinary services are those provided by a treatment team in which all of its
members participate in a coordinated effort to benefit the patient and the patient’s
significant others and caregivers. Interdisciplinary services, by definition, cannot be
provided by only one discipline. Though individual members of the interdisciplinary
team work within their own scopes of practice, each professional is also expected to
coordinate his or her efforts with team members of other specialties, as well as with the
patient and the patient’s significant others and caregivers. The purpose of the
interdisciplinary team is to foster frequent, structured, and documented communication
among disciplines to establish, prioritize, and achieve treatment goals.
The periodic team conferences—held a minimum of once per week—must focus on:
• Assessing the individual's progress towards the rehabilitation goals;
• Considering possible resolutions to any problems that could impede progress towards
the goals;
A team conference may be formal or informal; however, a review by the various team
members of each other's notes does not constitute a team conference. It is expected that
all treating professionals from the required disciplines will be at every meeting or, in the
infrequent case of an absence, be represented by another person of the same discipline
who has current knowledge of the patient. Documentation of each team conference must
include the names and professional designations of the participants in the team
conference. The occurrence of the team conferences and the decisions made during such
conferences, such as those concerning discharge planning and the need for any
adjustment in goals or in the prescribed treatment program, must be recorded in the
patient’s medical record in the IRF. The focus of the review of this requirement will be
on the accuracy and quality of the information and decision-making, not on the internal
processes used by the IRF in conducting the team conferences.
Since discharge planning is an integral part of any rehabilitation program and must begin
upon the patient’s admission to the IRF, an extended period of time for discharge from
the IRF would not be reasonable and necessary after established goals have been reached
or the determination has been made that further progress is unlikely.
For an IRF stay to be considered reasonable and necessary, the patient does not have to
be expected to achieve complete independence in the domain of self-care or return to his
or her prior level of functioning. However, to justify the need for a continued IRF stay,
the documentation in the IRF medical record must demonstrate the patient’s ongoing
requirement for an intensive level of rehabilitation services (as defined in section 110.2.1)
and an inter-disciplinary team approach to care (as defined in section 110.2.2). Further,
the IRF medical record must also demonstrate that the patient is making functional
improvements that are ongoing and sustainable, as well as of practical value, measured
against his/her condition at the start of treatment. Since in most instances the goal of an
IRF stay is to enable a patient’s safe return to the home or community-based environment
upon discharge, the patient’s treatment goals and achievements during an IRF admission
are expected to reflect significant and timely progress toward this end result. During
most IRF stays, therefore, the emphasis of therapies would generally shift from
traditional, patient-centered therapeutic services to patient/caregiver education, durable
medical equipment training, and other similar therapies that prepare the patient for a safe
discharge to the home or community-based environment.
CMS notes that as evidenced by the criteria established above, an IRF claim could never
be denied for the following reasons: (1) because a patient could not be expected to
achieve complete independence in the domain of self-care or (2) because a patient could
not be expected to return to his or her prior level of functioning.
Medical and hospital services are sometimes required to treat a condition that arises as a
result of services that are not covered because they are determined to be not reasonable
and necessary or because they are excluded from coverage for other reasons. Services
"related to" non-covered services (e.g., cosmetic surgery, non-covered organ transplants,
non-covered artificial organ implants, etc.), including services related to follow-up care
and complications of non-covered services which require treatment during a hospital stay
in which the non-covered service was performed, are not covered services under
Medicare. Services "not related to" non-covered services are covered under Medicare.
Following are examples of services "related to" and "not related to" non-covered services
while the beneficiary is an inpatient:
• A beneficiary was admitted to the hospital for covered services, but during the
course of hospitalization became a candidate for a non-covered transplant or
implant and actually received the transplant or implant during that hospital
stay. When the original admission was entirely unrelated to the diagnosis that
led to a recommendation for a non-covered transplant or implant, the services
related to the admitting condition would be covered.
• A beneficiary was admitted to the hospital for covered services related to a
condition which ultimately led to identification of a need for transplant and
receipt of a transplant during the same hospital stay. If, on the basis of the
nature of the services and a comparison of the date they are received with the
date on which the beneficiary is identified as a transplant candidate, the
services could reasonably be attributed to preparation for the non-covered
transplant, the services would be "related to" non-covered services and would
also be non-covered.
After a beneficiary has been discharged from the hospital stay in which the beneficiary
received non-covered services, medical and hospital services required to treat a condition
or complication that arises as a result of the prior non-covered services may be covered
when they are reasonable and necessary in all other respects. Thus, coverage could be
provided for subsequent inpatient stays or outpatient treatment ordinarily covered by
Medicare, even if the need for treatment arose because of a previous non-covered
procedure. Some examples of services that may be found to be covered under this policy
are the reversal of intestinal bypass surgery for obesity, complications from cosmetic
surgery, removal of a non-covered bladder stimulator, or treatment of any infection at the
surgical site of a non-covered transplant that occurred following discharge from the
hospital.
However, any subsequent services that could be expected to have been incorporated into
a global fee are not covered. Thus, where a patient undergoes cosmetic surgery and the
treatment regimen calls for a series of postoperative visits to the surgeon for evaluating
the patient's progress, these visits are not covered.
Section 1821 of the Social Security Act provides for coverage of services furnished in a
Medicare qualified religious nonmedical health care institution (RNHCI), when the
beneficiary meets specific coverage conditions. The beneficiary must have a valid
election for RNHCI services and would otherwise qualify for care in a conventional
hospital or post hospital extended care facility that was not a religious nonmedical health
care institution.
The RNHCI benefit provides only for Part A inpatient services. The Medicare program
will only pay for nonmedical health care services furnished in RNHCIs, as defined in
Section 1861(ss)(1) of the Act and 42 CFR 403 Subpart G. The program does not pay for
supporting religious services or payment for the religious practitioner. The cost of
religious items/services and the cost of using a religious practitioner is a personal
financial responsibility and not covered by Medicare.
A beneficiary may elect to receive care in an RNHCI based on his or her own religious
convictions or to revoke that election at any time if for any reason he or she decides to
pursue medical care. Section 1821(a) of the Act requires that as a condition for Part A
Medicare coverage, the beneficiary must have a condition that would qualify under
Medicare Part A for inpatient hospital services or extended care services furnished in a
hospital or skilled nursing facility that is not an RNHCI if it were not for their religious
convictions.
When a beneficiary has an effective election on file with CMS but does not have a
condition that would qualify for Medicare Part A inpatient hospital or posthospital
extended care services if the beneficiary were an inpatient of a hospital or a resident of a
SNF that is not an RNHCI, then services furnished in an RNHCI are not covered by
Medicare. A Medicare claim for services that were furnished to that beneficiary would
be treated as a claim for noncovered services. If the beneficiary only needs assistance
with activities of daily living, then the beneficiary's condition could not be considered as
meeting the Medicare Part A requirements. Prior to submitting a claim to Medicare it is
the responsibility of the RNHCI’s utilization review committee to determine that the
beneficiary meets the Medicare Part A requirements.
If no valid election is filed or the election has been revoked and no new election is in
effect, the beneficiary does not have Medicare coverage for services furnished in an
RNHCI. Consequently, a Medicare claim for services furnished to such a beneficiary
would also be treated as a claim for noncovered services.
In those cases where a beneficiary is admitted to an RNHCI with a valid election, the
submission of prior claim for medical services to the Common Working File will revoke
the election during the course of the RNHCI stay. If this is the first revocation, the
beneficiary may make a new election without any disruption to the benefit. If this,
however, is the second or subsequent revocation, the applicable waiting period applies
and the remainder of the stay is not covered by Medicare (see 130.2.2).
For an RNHCI to receive payment under the Medicare program, the beneficiary must
make a written election to receive benefits under §1821 of the Act. To elect religious
nonmedical health care services, the beneficiary or the beneficiary’s legal representative
must attest that the individual is conscientiously opposed to acceptance of nonexcepted
medical treatment, and the individual’s acceptance of such treatment would be
inconsistent with the individual’s sincere religious beliefs.
Religious non-medical care or religious method of healing means health care furnished
under established religious tenets that prohibit conventional or unconventional medical
care for the treatment of a beneficiary, and the sole reliance on these religious tenets to
fulfill a beneficiary's total health care needs.
Medical care or treatment means health care furnished by or under the direction of a
licensed physician that can involve diagnosing, treating, or preventing disease and other
damage to the mind and body. It may involve the use of pharmaceuticals, diet, exercise,
surgical intervention, and technical procedures.
The signed and notarized election must include a statement that the receipt of
nonexcepted medical services would constitute a revocation of the election and may limit
further receipt of payment of religious nonmedical health care services. The election is
effective on the date it is signed, and it remains in effect until revoked in writing or by the
receipt and filing of a claim for nonexcepted medical treatment.
The completed election form must be filed with the specialty contractor, a copy retained
by the RNHCI provider and a copy provided to the beneficiary. See Pub. 100-04,
Medicare Claims Processing Manual, Chapter 3, Section 170 for instructions on
submission of elections to the specialty contractor.
Section 1821 defines “excepted” medical treatment as medical care or treatment that is
received involuntarily or is required under Federal, State or local law. The term is
intended to identify the kinds of medical services that can be provided to a beneficiary
with an election for RNHCI services without revoking the election.
Examples of excepted medical care include, but are not limited to the following:
Examples of nonexcepted medical care could include but are not limited to the following:
• A beneficiary receiving medical diagnosis and/or treatment for persistent
headaches and/or chest pains.
Note that the terms ‘excepted’ and ‘nonexcepted’ care represent mutually exclusive
conditions under §1821 of the Social Security Act. Medicare contractors may use the
examples above in making determinations of excepted and nonexcepted care.
Revocation is the cancellation of the RNHCI election and can be achieved in two ways:
either by submitting a written statement to the intermediary indicating the desire to cancel
the election or by seeking nonexcepted medical care for which Medicare payment is
sought.
See Pub. 100-04, Medicare Claims Processing Manual, Chapter 3, Section 170 for
instructions on submission of revocations to the specialty contractor. See section 180 of
that manual for a description of how Medicare non-specialty contractors revoke elections
upon billing for nonexcepted services.
After an initial revocation, the individual may again file a written election to receive the
religious nonmedical health care benefit. This second election takes effect immediately
upon its execution. If an individual revokes a second election, the next (third) election
cannot become effective until 1 year after the date of the most recent revocation.
Subsequent elections are not effective until 5 years after the most recent revocation. Once
an election is revoked, Medicare payment cannot be made to an RNHCI unless a valid
election is filed. The RNHCI revocation does not interfere with the beneficiary’s ability
to seek other Medicare services within the limits of his/her Medicare coverage.
Under normal Medicare rules, a provider of services may only bill a beneficiary
deductible and coinsurance amounts. However, total Medicare payments to RNHCIs are
subject to limits established in sections 1821(c)(2) (A) or (B) of the Act. In the event that
the Medicare program reduces payments to RNHCIs based on these limits, RNHCIs may
also bill beneficiaries an amount equal to any such reduction.
Prior to the passage of the Medicare Prescription Drug, Improvement and Modernization
Act (MMA) of 2003, the Medicare program’s RNHCI benefit was limited to inpatient
services provided in an RNHCI facility. The MMA revised sections 1821(a) and 1861 of
the Social Security Act to extend coverage to RNHCI items and services that are
provided in a beneficiary’s home and that are comparable to items and services provided
by a home health agency that is not an RNHCI.
Beneficiaries elect the RNHCI benefit if they are conscientiously opposed to accepting
most medical treatment, since accepting such services would be inconsistent with their
sincere religious beliefs. The Medicare home health benefit provides skilled nursing,
physical therapy, occupational therapy, speech language pathology and home health aide
services to eligible beneficiaries under a physician’s plan of care. The home health
benefit also provides medical supplies, a covered osteoporosis drug and durable medical
equipment (DME) while under a plan of care (see chapter 7).
Medicare covers specified durable medical equipment and intermittent RNHCI nursing
visits provided in the home to RNHCI beneficiaries. These services comprise the RNHCI
home benefit. The remainder of the services covered under the Medicare home health
benefit are medical in nature and must be provided under the order of a physician. As
such, these services conflict with RNHCI beneficiaries’ conscientious opposition to
medical care.
The RNHCI home benefit must exclude the same services that are excluded from the
home health benefit, which include: drugs and biologicals; transportation; services that
would not be covered as inpatient services; housekeeping services; services covered
under the End Stage Renal Disease program; prosthetic devices; and medical social
services provided to family members. These exclusions are defined at 42 CFR 409.49.
Additionally, the RNHCI home benefit excludes the items or services provided by any
HHA that is not an RNHCI; or any supplier, independent RNHCI nurse or aide that is
working directly for a beneficiary rather than under arrangements with the RNHCI.
Medicare requires a brief letter of intent from the provider in order to determine the
number of RNHCIs that will be implementing the home service benefit.
In the case where an RNHCI chooses to provide home services then only care on an
intermittent basis, which is provided to an eligible beneficiary who is confined to their
home for health reasons, will be covered under the home benefit. The home benefit is not
to be confused with hospice care, which may involve more frequent visits and can
involve institutional services. If for some reason the home serviced patient requires more
than intermittent service, then institutional services may be required. However, the
patient would need to meet the criteria for admission to a RNHCI, or the patient would
require another institutional setting not necessarily covered by Medicare.
Similar to the inpatient RNHCI benefit, the physician role in certifying and ordering the
home benefit is replaced with the use of the RNHCI utilization review committee to
review the need for care and plan for initial and continued care in the home setting. The
home benefit will also require a prompt review of admission to the home service, since
the patient must be fully eligible (have a health condition that keeps them confined to the
home (42CFR409.42(a), have health needs that can be met with intermittent care, and
have a valid election) before billable services can be rendered and Medicare payment
requested. Additionally the utilization review committee is responsible for review and
approval of care plans and orders for DME items, and review of the need for the
continuation of services.
As in the original RNHCI benefit, Medicare will only pay for nonmedical services in the
home, but not for those religious items or services provided by the RNHCI.
Medicare covers these items and services for dates of service from January 1, 2005
through December 30, 2006. Total Medicare payments under this benefit for each
calendar year during this period are limited to $700,000.
Medicare covers a defined list of nonmedical DME items for RNHCI home services that
are comparable to items used in the inpatient RNHCI setting and could be provided by an
HHA. The DME items include canes, crutches, walkers, commodes, a standard
wheelchair, hospital beds, bedpans, and urinals. Those RNHCIs offering home services
may order these items without a physician order and without compromising the
beneficiary election for RNHCI care. The need for each item of DME ordered must be
supported by the RNHCI patient’s plan of care for the home setting and the RNHCI
nurses’ notes for home services. It must be noted that the benefit is applicable only to
what we shall refer to as “nonmedical DME items” and does not include any of the
related services provided by RNHCI staff members.
The RNHCI shall establish a payment arrangement with one or more DME suppliers to
obtain any of the items on the DME list (below) they may require for a beneficiary. The
supplier will provide the items and related instructions on use to the
beneficiary/family/care giver. The RNHCI will submit claims for these DME items to
the RNHCI specialty FI.
The RNHCI must stress to suppliers that DME claims are not to be submitted to the
DMERC because this will cause the beneficiary’s election for RNHCI care to be revoked.
DME Items and HCPCS Codes for use by RNHCI Home Service Units Canes
E0100 Cane, includes canes of all materials, adjustable or fixed, with tip
E0105 Cane, quad or three prong, includes canes of all materials, adjustable or fixed with
tip
Crutches
E0112 Crutches, underarm, wood, adjustable or fixed, pair, with pads, tips and handgrips
E0113 Crutch underarm, wood, adjustable or fixed, pair, with pad, tip and handgrip
E0114 Crutches, underarm, other than wood, adjustable or fixed, pair, with pads, tips and
handgrips
E0116 Crutch underarm, other than wood, adjustable or fixed, with pad, tip and handgrip
Walkers
Commodes
Wheelchairs
E0250 Hospital bed, fixed height, with any type side rails, with mattress
E0255 Hospital bed, variable height, hi-lo, with any type side rails, with mattress
E0260 Hospital bed, semi-electric (head and foot adjustment), with any type side rails,
with mattress
E0290 Hospital bed, fixed height, without side rails, with mattress
E0292 Hospital bed, variable height, hi-lo, without side rails, with mattress
Payment to RNHCIs for these specified DME items will be made based on the DME fee
schedule. Coinsurance applies to these items. Deductible does not apply to these items.
Medicare covers intermittent RNHCI nursing visits provided in the home to RNHCI
beneficiaries. The RNHCI nursing personnel may be skilled in ministering to a
beneficiary’s religious needs (not covered by Medicare), but do not have the training or
nursing skill sets required of credentialed/licensed health care professionals (e.g.,
registered nurse). While RNHCI nurses may provide tender loving care, they are focused
primarily on religious healing and meeting basic beneficiary needs for assistance with
activities of daily living (e.g., bathing, toileting, dressing, ambulation), as part of creating
a milieu for religious healing. The care provided by an RNHCI nurse is not at the level
of either a registered nurse or a licensed practical nurse. The physical care provided by
an RNHCI nurse is at a level that could be considered as supportive, but decidedly not
“skilled” as defined by the Medicare program.
For purposes of payment for RNHCI nursing services in the home, the following services
are comparable to the services of HHAs that are not RNHCIs (e.g., the RNHCI nurse and
the home health aide share the following basic tasks):
• Assist with activities of daily living which include: ambulation, bed to
chair transfer, and assist with range of motion exercises; bathing,
shampoo, nail care and dressing; feeding and nutrition; and toileting;
• Documenting visit
By comparison the home health aide will routinely perform additional medically oriented
services (e.g., observation and reporting of existing medical conditions, taking and
reporting vital signs, and using basic infection control procedures).
Due to the uniqueness of RNHCI nursing in the Medicare program, Medicare pays for
RNHCI nursing visits at a percentage of the HHAs “low utilization payment adjustment”
(LUPA) rate for home health aides. Only a visit by an RNHCI nurse to a home will be
considered as billable to Medicare. A visit is defined as an episode in which an RNHCI
nurse will render physical care to an RHNCI beneficiary in the home setting. The visit is
a single billable unit that is not influenced by the number of involved caregivers or the
duration of the episode. The difference in skill levels and the incorporation of RNHCI
religious activity (noncovered by Medicare) into a visit, resulted in a payment rate that is
80% of the home health aide rate adjusted by metropolitan service area (MSA) wage
index rate for the involved RNHCI.
RNHCI nursing visits are paid using the LUPA system even in situations where the
involved patient would not be classified as low utilization. The HHAs have moved to
PPS, which is constructed on the medical model and therefore inappropriate for RNHCI
use. The same “labor”/”non-labor” portions applied in the HHA PPS will be used for
calculating the RNHCI nursing visit payments.
1. Home Health Aide Visit (National standardized rate for 2005) $44.76
Step 1. Take the HHA aide visit base rate ($ 44. 76) for the involved year (2005), from
the HHA update published annually each November in the Federal Register.
Step 2. To calculate the RNHCI nurse visit base rate, multiply the HHA base rate ($
44.76) by the allowed percentage for an RNHCI nurse visit (.80%) to allow for
religious activity and reduced physical care skill level = ($ 35.81)
Step 3. To calculate the labor portion of the Standardized Budget Neutral Per-Visit
Payment Amount for 1 RNHCI nurse visit, multiply the fixed allowance .76775
by the RNHCI nurse visit rate ($ 35.81) = ($ 27.49)
Step 4. Apply the wage index for the involved MSA from the HHA update published
annually each November in the Federal Register (Baltimore, MD = .9907)
multiplied by the labor portion of the RNHCI nurse visit ($ 27.49) = ($27.23).
Step 5. To calculate the non-labor portion of the Standardized Budget Neutral Per-Visit
Payment Amount for 1 RNHCI nurse visit, multiply the fixed allowance .23225
by the RNHCI nurse visit rate ($ 35.81) = ($ 8.32)
Step 6. To calculate the LUPA rate for 1 RNHCI nurse visit add the products from Step 4
($27.49) and Step 5 ($ 8.32) = ($ 35.55)
Step 7. To calculate the LUPA payment for RNHCI nurse visits to one beneficiary in a 30
day period, multiply the product of Step 6 ($ 35.55) by the number of visits (12) = ($
426.60)
Transmittals Issued for this Chapter