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pdfDEPARTMENT OF HEALTH AND HUMAN SERVICES
CENTERS FOR MEDICARE & MEDICAID SERVICES
Form Approved
OMB No.
CERTIFICATE OF MEDICAL NECESSITY
DME 03.XX
POSITIVE AIRWAY PRESSURE (PAP) DEVICES FOR OBSTRUCTIVE SLEEP APNEA
SECTION A
Certification Type/Date:
INITIAL ___/___/___
RECERTIFICATION ___/___/___
PATIENT NAME, ADDRESS, TELEPHONE and HIC NUMBER
SUPPLIER NAME, ADDRESS, TELEPHONE and NPI
(__ __ __) __ __ __ - __ __ __ __ HICN ____________________________
(__ __ __) __ __ __ - __ __ __ __ NPI # __________________________________
PLACE OF SERVICE ________
PT DOB ____/____/____; Sex ____ (M/F) ;
HCPCS CODE
HT.______(in.) ;
WT._____(lbs.)
PHYSICIAN NAME, ADDRESS (Printed or Typed)
NAME and ADDRESS of FACILITY if applicable (See
Reverse)
PHYSICIAN’S NPI: ______________________________
PHYSICIAN’S TELEPHONE #: (__ __ __) __ __ __- __ __ __ __
SECTION B
Information in this Section May Not Be Completed by the Supplier of the Items/Supplies.
EST. LENGTH OF NEED (# OF MONTHS): ______ 1-99 (99=LIFETIME)
ANSWERS
DIAGNOSIS CODES (ICD-9): _________ _________ _________ _________
ANSWER QUESTIONS 1-6 FOR INITIAL EVALUATION
ANSWER QUESTIONS 7-9 FOR FOLLOW-UP EVALUATION (RECERTIFICATION)
(Circle Y for Yes, N for No, D for Does Not Apply)
1. Is the device being ordered for the treatment of obstructive sleep apnea (ICD-9 diagnosis code 327.23)?
Y
N
If YES, continue to Questions 2-5; If NO, Proceed to Section D
__/__/__
2. Enter date of initial face-to-face evaluation
___/___/___
Y
N
3. Enter date of sleep test (If test spans multiple days, enter date of first day of test)
4. Was the patient’s sleep test conducted in a facility-based lab?
_________
5. What is the patient’s Apnea-Hypopnea Index (AHI) or Respiratory Disturbance Index (RDI)?
Y
6. If a bilevel device is ordered, has a CPAP device been tried and found ineffective?
N
D
__/__/__
7. Enter date of follow-up face-to-face evaluation
Y
N
8. Is there a report documenting that the patient used CPAP ≥ 4 hours per night on at least 70% of nights in a 30 consecutive
day period?
Y
N
9. Did the patient demonstrate improvement in symptoms of obstructive sleep apnea with the use of CPAP?
NAME OF PERSON ANSWERING SECTION B QUESTIONS, IF OTHER THAN PHYSICIAN (Please Print):
NAME: ____________________________________________ TITLE: ________________________ EMPLOYER: _________________________
SECTION C
Narrative Description Of Equipment And Cost
(1) Narrative description of all items, accessories and options ordered; (2) Supplier’s charge; and (3) Medicare Fee Schedule
Allowance for each item, accessory, and option. (See Instructions On Back)
SECTION D
Physician Attestation and Signature/Date
I certify that I am the physician identified in Section A of this form. I have received Sections A, B and C of the Certificate of Medical Necessity (including charges for
items ordered). Any statement on my letterhead attached hereto, has been reviewed and signed by me. I certify that the medical necessity information in Section
B is true, accurate and complete, to the best of my knowledge, and I understand that any falsification, omission, or concealment of material fact in that section may
subject me to civil or criminal liability.
PHYSICIAN’S SIGNATURE ______________________________________ DATE _____/_____/_____ (SIGNATURE AND DATE STAMPS ARE ACCEPTABLE)
Form CMS-10269 (06/08)
INSTRUCTIONS FOR COMPLETING THE CERTIFICATE OF MEDICAL NECESSITY
FOR CONTINUOUS POSITIVE AIRWAY PRESSURE (CPAP) (CMS-10269)
SECTION A:
(May be completed by the supplier)
CERTIFICATION TYPE/
DATE:
If this is an initial certification for this patient, indicate this by placing date (MM/DD/YY) needed initially in the space
marked “INITIAL.” If this is a revised certification (to be completed when the physician changes the order, based on
the patient’s changing clinical needs), indicate the initial date needed in the space marked “INITIAL,” and also indicate
the recertification date in the space marked “REVISED.” If this is a recertification, indicate the initial date needed in the
space marked “INITIAL,” and also indicate the recertification date in the space marked “RECERTIFICATION.” Whether
submitting a REVISED or a RECERTIFIED CMN, be sure to always furnish the INITIAL date as well as the REVISED or
RECERTIFICATION date.
PATIENT
INFORMATION:
Indicate the patient’s name, permanent legal address, telephone number and his/her health insurance claim number (HICN)
as it appears on his/her Medicare card and on the claim form.
SUPPLIER INFORMATION:
Indicate the name of your company (supplier name), address and telephone number along with the National Provider
Identification (NPI) number assigned to you by the National Supplier Clearinghouse (NSC).
PLACE OF SERVICE:
Indicate the place in which the item is being used, i.e., patient’s home is 12, skilled nursing facility (SNF) is 31, End Stage
Renal Disease (ESRD) facility is 65, etc. Refer to the DME MAC supplier manual for a complete list.
FACILITY NAME:
If the place of service is a facility, indicate the name and complete address of the facility.
HCPCS CODES:
List all HCPCS procedure codes for items ordered that require a CMN. Procedure codes that do not require certification
should not be listed on the CMN.
PATIENT DOB, HEIGHT,
WEIGHT AND SEX:
Indicate patient’s date of birth (MM/DD/YY) and sex (male or female); height in inches and weight in pounds, if requested.
PHYSICIAN NAME,
ADDRESS:
Indicate the physician’s name and complete mailing address.
NPI:
Accurately indicate the ordering physician’s National Provider Identification number (NPI).
PHYSICIAN’S
TELEPHONE NO:
Indicate the telephone number where the physician can be contacted (preferably where records would be accessible pertaining
to this patient) if more information is needed.
SECTION B:
(May not be completed by the supplier. While this section may be completed by a non-physician clinician, or a
physician employee, it must be reviewed, and the CMN signed (in Section D) by the ordering physician.)
EST. LENGTH OF NEED:
Indicate the estimated length of need (the length of time the physician expects the patient to require use of the ordered item)
by filling in the appropriate number of months. If the physician expects that the patient will require the item for the duration of
his/her life, then enter 99.
DIAGNOSIS CODES:
In the first space, list the ICD9 code that represents the primary reason for ordering this item. List any additional ICD9 codes
that would further describe the medical need for the item (up to 3 codes).
QUESTION SECTION:
This section is used to gather clinical information to determine medical necessity. Answer each question which applies to the
items ordered, circling “Y” for yes, “N” for no, or fill in the blank if other information is requested.
NAME OF PERSON
ANSWERING SECTION B
QUESTIONS:
If a clinical professional other than the ordering physician (e.g., home health nurse, physical therapist, dietician)
SECTION C:
(To be completed by the supplier)
NARRATIVE
DESCRIPTION OF
EQUIPMENT & COST:
Supplier gives (1) a narrative description of the item(s) ordered, as well as all options, accessories, supplies and drugs;
(2) the supplier’s charge for each item, option, accessory, supply and drug; and (3) the Medicare fee schedule allowance for
each item/option/accessory/supply/drug, if applicable.
SECTION D:
(To be completed by the physician)
PHYSICIAN
ATTESTATION:
The physician’s signature certifies (1) the CMN which he/she is reviewing includes Sections A, B, C and D; (2) the answers
in Section B are correct; and (3) the self-identifying information in Section A is correct.
PHYSICIAN SIGNATURE
AND DATE:
After completion and/or review by the physician of Sections A, B and C, the physician must sign and date the CMN in
Section D, verifying the Attestation appearing in this Section. The physician’s signature also certifies the items ordered are
medically necessary for this patient. Signature and date stamps are not acceptable.
or a physician employee answers the questions of Section B, he/she must print his/her name, give his/her professional title
and the name of his/her employer where indicated. If the physician is answering the questions, this space may be left blank.
According to the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it displays a valid OMB control number. The valid OMB control number for this
information collection is 0938-0679. The time required to complete this information collection is estimated to average 15 minutes per response, including the time to review instructions, search existing resources,
gather the data needed, and complete and review the information collection. If you have any comments concerning the accuracy of the time estimate or suggestions for improving this form, please write to: CMS,
7500 Security Blvd., N2-14-26, Baltimore, Maryland 21244-1850.
Form CMS-10269 (06/08)
File Type | application/pdf |
File Modified | 2008-07-17 |
File Created | 2008-07-01 |