F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure that a resident who needs respiratory
care, is provided such care, consistent with professional standards of practice for 2 (Resident #1 and
Resident #2) of 4 residents reviewed for respiratory care.
Residents Affected - Few
The facility failed to ensure that Resident #1's oxygen tubing with nasal cannula and humidifier bottle was
replaced every seven (7) days.
The facility failed to ensure that Resident #1's air concentrator filter was cleaned and free of dust and debris
particles.
The facility failed to ensure that Resident #2's Nebulizer tubing and mask, which included the nebulizing
chamber (unit into which liquid medicine is converted into aerosol or mist by the pressurized air pumped
through the tubing), was replaced every seven (7) days.
These failures could place residents at risk for respiratory compromise and infection.
Findings Included:
A) Review of Resident #1's Face Sheet dated 06/20/2024 reflected a [AGE] year-old female admitted to the
facility on [DATE] with the following diagnoses: Unspecified Dementia (condition characterized by
progressive or persistent loss of intellectual functioning, especially with impairment of memory and abstract
thinking, and often with personality change, resulting from disease of the brain) and Dysphagia (swallowing
difficulties).
Review of Resident #1's MDS Comprehensive Assessment, dated 03/14/2024 revealed Resident #1 had a
BIMS Score of 13, which indicated cognition was intact. Resident #1's MDS indicated for Respiratory
Treatments that she was under C1. Oxygen therapy, which occurred while she was a resident.
Review of Resident #1's Comprehensive Care Plan revealed The resident has Oxygen Therapy, PRN with
an intervention for Oxygen at 2L/min per nasal cannula if O2 sat<90% or if Res feels SOB, with both
revised on 10/07/2020.
Review of Resident #1's Order Summary Report reflected an indefinite order on 03/12/2022 for May have
O2 @ 2L/min via NC continuously with directions for every shift for sob/wheezing related to GENERALIZED
ANXIETY DISORDER. Further review revealed an indefinite order on 4/6/2023 for Change respiratory
concentrator water, clean filter q7d with directions for every night shift every Sun.
(continued on next page)
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 3
Event ID:
676385
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
676385
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Crossroads Nursing & Rehabilitation
611 Rose Marie Blvd
Hearne, TX 77859
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Review of Resident #1's Treatment Administration Record from 06/1/2024 - 06/20/2024 reflected, Change
respiratory concentrator water, clean filter q7d every night shift every Sun and indicated it was completed
on Sunday, 06/02/2024, Sunday, 06/09/2024, and Sunday, 06/16/2024.
Observation on 06/20/2024 at 12:00 PM, Resident #1 was in her bed receiving oxygen via nasal cannula
from an air concentrator. A check of her oxygen tubing and concentrator revealed the humidifier bottle had
6-10-24 recorded on the top of it, with no date present on the tubing. Resident #1 was receiving air from the
concentrator at 2L per minute and a check of the filter on the back of it revealed it was covered in dust and
debris particles.
Interview and observation on 06/20/2024 at 2:56 PM, Resident #1 had her tubing and nasal cannula
hanging off the side of her bed side table and stated it was off because she just received a bath. Resident
#1's humidifier bottle had the same date as earlier observation and had not been changed. Resident #1
stated that her oxygen tubing and cannula were not changed on 06/20/2024 but stated they do change it
out. Resident #1 stated that she could not recall in days or weeks when the last time was that they changed
out her oxygen tubing with cannula.
B) Review of Resident #2's Face Sheet dated 06/20/2024 reflected a [AGE] year-old female admitted to the
facility on [DATE] with the following diagnoses: Athetoid Cerebral Palsy (movement disorder cause by
damage to the developing brain characterized by abnormal, involuntary movement), Cystic Fibrosis
(disease that causes thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the
body), and Unspecified Dementia (condition characterized by progressive or persistent loss of intellectual
functioning, especially with impairment of memory and abstract thinking, and often with personality change,
resulting from disease of the brain).
Review of Resident #2's Quarterly MDS Assessment, dated 05/23/2024 revealed Resident #2 had a BIMS
Score of 00, which indicated severe cognitive impairment. Resident #2's MDS indicated for Respiratory
Treatments that she was under C1. Oxygen therapy, which occurred while she was a resident.
Review of Resident #2's Comprehensive Care Plan revealed The resident has impaired cognitive function
r/t dementia dx with an intervention for Administer meds as ordered, with both revised on 08/28/2023.
Resident #2's Comprehensive Care Plan did not specifically address the use of her nebulizer.
Review of Resident #2's Order Summary Report reflected an order on 08/15/2023 for Ipratropium-Albuterol
Inhalation Solution 0.5-2.5 (3) MG/3ML with directions for 1 dose via trach every 4 hours.
Review of Resident #2's Treatment Administration Record from 06/1/2024 - 06/20/2024 reflected,
Ipratropium-Albuterol Inhalation Solution 0.5-2.5 (3) MG/3ML (Ipratropium-Albuterol) 1 dose via trach every
4 hours as needed for Shortness of Breath; Wheezing documented as PRN with no indication of treatment
for dates reviewed. The Treatment Administration Record further reflected Change Nebulizer Tubing and
Delivery Device every 8 hours as needed related to UNSPECIFIED TRACHEOSTOMY COMPLICATION
documented as PRN with no notations of completion for the dates reviewed.
Observation on 06/20/2024 at 12:04 PM, revealed that Resident #2 was in her bed with a nebulizer present
on her nightstand, with a plastic bag in front of it. The bag had Resident #2's last name recorded on the
front of it as well as 6/3. The bag contained tubing and a mask with attached nebulizing chamber, none of
which had a date recorded on them.
Interview and observation on 06/20/2024 at 2:58 PM, revealed that Resident #2's nebulizer mask with
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676385
If continuation sheet
Page 2 of 3
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
676385
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/20/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Crossroads Nursing & Rehabilitation
611 Rose Marie Blvd
Hearne, TX 77859
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
chamber and tubing remained bagged at her bedside with a date of 6/3. Resident #2 was not interviewable
but acknowledged with a smile that she was alright when questioned.
Interview on 06/20/2024 at 3:22 PM, LVN B stated all respiratory equipment including mask, cannulas,
tubing, and humidifier bottles are to be changed out every seven days by a nurse on Sunday night. LVN B
stated they are also supposed to clean the filter on the residents' air concentrator at the same time. LVN B
stated they normally record the date of change on the humidifier bottle for concentrated air and on the
mask or the outside of the bag for nebulizer equipment. LVN B stated that failure to properly change and
maintain oxygen / nebulizer equipment increases a resident's chance of respiratory infection.
Interview on 06/20/2024 at 3:35 PM, RN A stated oxygen and nebulizer equipment are to be changed out
every Sunday night by a nurse or more frequently if they become soiled. RN A stated oxygen tubing with
cannulas have the date recorded on a piece of tape that is stuck to the tubing or have the date recorded on
the humidifier bottle, because they are supposed to be changed at the same time. RN A stated dates for
nebulizer equipment can be placed on the mask itself or the outside of the bag. RN A stated failure to
properly change out oxygen equipment could lead to respiratory issues for the resident.
Interview and observation on 06/20/2024 at 3:37 PM, the ADON stated mask, tubing, cannulas, and
humidifier bottles are to be changed out every seven days by the night nurse on Saturday to Sunday. The
ADON stated the filters on air concentrators are also to be cleaned every seven days or more often if
necessary. The ADON stated when they change out oxygen tubing with cannulas and the humidifier bottle,
they will record the date on the bottle or will place the date on the tubing at the concentrator port. The
ADON stated failure to properly change and maintain respiratory equipment could result in illness or
worsen a resident's condition. At 3:39 PM, the ADON entered the room of Resident #1 and checked her
oxygen concentrator and equipment. The ADON stated it was not correct because it had not been changed
out within the past seven days. The ADON stated the filter on the concentrator had also not been cleaned in
over seven days based off the dust and debris build up on it. At 3:45 PM, the ADON entered the room of
Resident #2 and checked her nebulizer and equipment. The ADON stated that Resident #2's nebulizer
equipment was not correct and had not been changed out every seven days per their procedures.
Interview on 06/20/2024 at 4:00 PM, the Administrator stated her expectation was for all respiratory
equipment to be changed out weekly or more often if soiled. The Administrator stated that the documented
observations were not within policy and could result in illness.
Review of the facility's Respiratory Policies and Procedures Manual dated 6/1/2006 revealed, POLICY
TITLE: 10.0 Respiratory Equipment/Supply Disinfection/Cleaning, 9. In addition to surface disinfection,
perform the following: 9.4 Oxygen Concentrators: Rinse and dry the external filter weekly and prn when
visibly dusty. 11. Schedule for Supply Changes, Item, Nebulizers/Aerosols/Humidifiers, Frequency, Every 7
days. POLICY TITLE: 10.1 Oxygen Concentrators, PROCESS 9. Label, date and attach water bottle.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676385
If continuation sheet
Page 3 of 3