F 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to request, refuse, and/or discontinue treatment, to participate in or refuse to
participate in experimental research, and to formulate an advance directive.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review the facility failed to ensure all residents had the right to formulate an advanced
directive for 1 (Resident #38) of 25 residents reviewed for advanced directives. Resident #38 had a DNR in
her record that was signed incorrectly by the witnesses. The facility's failure could place residents at risk for
not receiving healthcare as per their or their legal representatives' wishes.Findings included: Record review
of Resident #38's face sheet printed [DATE] revealed she was a [AGE] year-old female resident admitted to
the facility on [DATE] with diagnoses to include chronic obstructive pulmonary disease (a group of lung
diseases that block airflow and make it difficult to breath), congestive heart failure (a chronic condition in
which the heart dose not pump blood as well as it should), cardiomegaly (enlargement of the heart), and
emphysema (a chronic lung condition where the tiny air sacs (alveoli) in the lungs become permanently
damaged and enlarged, making it hard to breathe and exhale air). Resident #38 was as a DNR in the
section Advance Directives. Resident #38's last MDS was a significant change of condition assessment
completed [DATE] listing her with a BIMS of 15 indicating she was cognitively intact, and she had a
functionality of requiring setup/clean-up assistance from staff with her activities of daily living. Resident
#38's care plan with admission date of [DATE] revealed the following: Problem:Resident has an order for Do
Not Resuscitate. Date initiated: [DATE]. Record review of the clinical record for Resident #38 revealed an
Order Summary printed [DATE] with the following order: DNR Active - Revision Date: [DATE]. Record review
of the clinical record for Resident #38 revealed a DNR dated [DATE] (signed by the physician) with the
following:Section - Two Witnesses: Both witness #1 and witness #2 did not date when they signed the
document. During an interview on [DATE] at 10:26 AM LVN A (the nurse responsible for Resident #38 this
shift) reported that all residents have their code status listed on the front/first page of their electronic chart,
and they have a code book on the unit that lists all residents' code status. LVN A reviewed Resident #38
electronic chart and printed code status and stated, Resident #38 is a DNR so we would not do CPR if she
had no heartbeat or was not breathing. LVN A reported she would notify management if Resident #38 was
to code (found with no heartbeat of was not breathing). When asked to review Resident #38's DNR form
listed in Resident #38's electronic record, LVN A reported both witnesses did not date their signatures
therefore the DNR form was not valid. LVN A stated, we would start CPR on her if she coded now. LVN A
reported if the DNR was not completed correctly it was not considered valid and would affect the resident
care, and the facility would not follow the residents' wishes. During an interview on [DATE] at 9:34 AM the
DON reported she had been made aware Resident #38 had the date missing from two signatures on her
DNR form. The DON reported she and her staff do a complete audit of all DNR's every 6 months and they
check for the proper signatures and just missed the dates. The DON reported if the DNR was incorrect then
the process will be done wrong for the residents, because you do not
(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 6
Event ID:
676461
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
676461
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Country View Living
701 Butler Blvd.
Dimmitt, TX 79027
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 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
have a legal paper. Record review of the facility provided policy titled Advanced Directives updated [DATE],
revealed the following: Policy Statement: Advanced Directives will be respected in accordance with state
law and facility policy. Record review of the OUT-OF-HOSPITAL DO-NOT-RESUSCITATE (OOH-DNR)
ORDER-TEXAS DEPARTMENT OF STATE HEALTH SERVICES, revised [DATE] revealed the
following:-The original or a copy of a fully and properly completed OOH-DNR Order or the presence of an
OOH-DNR device on a person is sufficient evidence of the existence of the original OOH-DNR Order and
either one shall be honored by responding health care professionals
Event ID:
Facility ID:
676461
If continuation sheet
Page 2 of 6
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
676461
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Country View Living
701 Butler Blvd.
Dimmitt, TX 79027
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 0641
Ensure each resident receives an accurate assessment.
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 an assessment accurately reflected a
resident's status for 1 (Resident #38) of 15 residents reviewed for accuracy of MDS assessments. -The
facility failed to accurately assess Resident #38 for the use of CPAP therapy on her significant change of
condition MDS assessment completed 10/07/2025. This failure to accurately assess a resident could place
residents at risk for inaccurate and incomplete MDS assessment which could result in residents not
receiving correct care and services. Findings included: Record review of Resident #38's face sheet printed
12/10/2025 revealed she was a [AGE] year-old female resident admitted to the facility on [DATE] with
diagnoses to include chronic obstructive pulmonary disease (a group of lung diseases that block airflow
and make it difficult to breath), obstructive sleep apnea (a sleep disorder that involves cessation or
significant decrease in airflow in the presence of breathing effort), congestive heart failure (a chronic
condition in which the heart dose not pump blood as well as it should), cardiomegaly (enlargement of the
heart), and emphysema (a chronic lung condition where the tiny air sacs (alveoli) in the lungs become
permanently damaged and enlarged, making it hard to breathe and exhale air). Resident #38's last MDS
was a significant change of condition assessment completed 10/07/2025 listing her with a BIMS of 15
indicating she was cognitively intact, and she had a functionality of requiring setup/clean-up assistance
from staff with her activities of daily living. Section O - Special Treatments, Procedures, and Programs G1.
Non-invasive Mechanical Ventilator BiPAP/CPAP - Resident #38 was not listed as having this therapy While
a Resident. Record review of Resident #38's care plan with admission date of 09/03/2024 revealed the
following: Problem: Resident #38 has altered respiratory status/difficulty breathing r/t COPD (a group of
lung diseases that block airflow and make it difficult to breath) . CPAP. Date initiated: 9/10/2024. Record
review of the clinical record for Resident #38 revealed an Order Summary Report with active orders as of
12/10/2025 with the following order:- BiPAP machine at night and PRN setting: in 12, out 7, rate 12,
O2-50% as needed related to DYSPNEA (difficulty breathing), UNSPECIFIED (R06.00) Active 02/07/2025.
During an observation and interview on 12/09/2025 at 10:08 AM Resident #38 was observed with a
CPAP/BiPAP machine on her bedside table. Resident #38 reported she used the machine nightly and the
care and staff were good. During an interview on 12/11/2025 at 9:30 AM MDS Coordinator B reviewed
Resident #38 Significant Change of Condition MDS completed 10/07/2025 and stated, We did this (the
Significant Change of Condition MDS) because she (Resident #38) came off of hospice and no I did not
address her use of CPAP therapy. MDS Coordinator B reported the CPAP therapy should have been
addressed, she (MDS Coordinator B) had completed the MDS assessment, and she did not know why the
CPAP therapy was missing. MDS Coordinator B reported if the CPAP was not addressed on the MDS then
the staff could miss administering the therapy if they review the MDS and the residents might not get their
care. MDS Coordinator B reported the facility follows the RAI manual for any policy related issues with the
MDS assessment. During an interview on 12/11/2025 at 9:38 AM the DON reported if an MDS was not
completed accurately then it was an issue. The DON reported the MDS should accurately reflect the
residents' condition or an adverse reaction could occur because the MDS was not correct for the residents
care. Record review of the Long Term Care Facility Resident Assessment Instrument 3.0 User's Manual
Version 1.18.11, dated October 2023 (RAI Manual) revealed the following: SECTION O: SPECIAL
TREATMENTS, PROCEDURES, ANDPROGRAMS Coding Instructions for Column b. While a
ResidentCheck all treatments, procedures, and programs that the resident received or performed
afteradmission/entry or reentry to the facility and within the last 14 days. If no treatments,procedures or
programs were received by, performed on, or participated in by the residentwithin the last
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676461
If continuation sheet
Page 3 of 6
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
676461
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Country View Living
701 Butler Blvd.
Dimmitt, TX 79027
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 0641
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
14 days or since admission/entry or reentry, check Z, None of the above. O0110G1, Non-invasive
Mechanical VentilatorCode any type of CPAP or BiPAP respiratory support devices that prevent airways
from closingby delivering slightly pressurized air through a mask or other device continuously or
viaelectronic cycling throughout the breathing cycle. The BiPAP/CPAP mask/device enables theindividual to
support their own spontaneous respiration by providing enough pressure whenthe individual inhales to
keep their airways open, unlike ventilators that breathe for theindividual. If a ventilator or respirator is being
used as a substitute for BiPAP/CPAP, code here.This item may be coded if the resident places or removes
their own BiPAP/CPAP mask/device.
Event ID:
Facility ID:
676461
If continuation sheet
Page 4 of 6
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
676461
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Country View Living
701 Butler Blvd.
Dimmitt, TX 79027
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
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 residents who need respiratory
care were provided with such care consistent with professional standards of practice for 1 (Resident #38) of
15 residents reviewed for respiratory care. -Resident #38 was not receiving oxygen at the correct dose. This
failure could affect residents by placing them at risk for respiratory compromise and associated
complications such as shortness of breath, confusion, respiratory failure, infection, and exacerbation of
their condition. Findings included:Record review of Resident #38's face sheet dated 12/10/2025 revealed an
[AGE] year-old female resident admitted to the facility on [DATE] with diagnoses to include Chronic
Obstructive Pulmonary Disease(airway inflammation and difficulty breathing), Obstructive Sleep Apnea(a
sleep disorder that involves cessation or significant decrease in airflow in the presence of breathing effort),
Chronic Respiratory failure with hypoxia(low oxygen levels in the blood), dependence on supplemental
oxygen(needs extra oxygen to breathe adequately) and need for assistance with personal care. Record
review of Resident #38's Significant Change MDS completed 10/07/2025 listed her with a BIMS of 15
indicating her cognition was intact. Resident #38 was listed as receiving oxygen therapy while a
resident.Record review of Resident #38's care plan revealed the following revision for oxygen on
10/03/2025 reflected Resident #38 had altered respiratory status related to COPD with an intervention for
supplemental oxygen via nasal cannula to maintain saturation at 92% and above, not to exceed 4 liters.
Record review of Resident #38's order summary reports revealed the following active orders: Oxygen via
nasal cannula at 4L/min continuously related to Chronic Obstructive Pulmonary Disease dated
02/07/2025.Record review of Resident #38's vitals from 09/11/2025 through 12/10/2025 revealed oxygen
saturation was above 92% via n/c.During an observation on 12/09/2025 at 10:08 AM Resident #38 was
sitting in her wheelchair and was wearing oxygen via nasal cannula at 2L/min Resident #38 stated she
wears her oxygen continuously and believed her supplemental oxygen was supposed to be at 2-3lpm.
Resident #38 felt she was getting enough oxygen and had no concerns. During an observation on
12/10/2025 at 10:27 AM Resident #38 was in her room watching television while sitting in her wheelchair
and was utilizing oxygen at 2L/min. During an interview on 12/10/2025 at 10:35 AM LVN B (the skilled staff
member responsible for Resident #38 this shift) checked Resident #38's oxygen and verified that the
current dose being administered was 2L/min. LVN B then reviewed Resident #38's physician orders and
noted Resident #38 was ordered to receive oxygen at 4L/min. LVN stated Resident #38's orders were
wrong, and the orders should be 2L/min and stated the physician and changed it from 4L/min to 2L/min and
it must not have been changed in the system. LVN B stated the 2 liters she was receiving was correct and
did not believe there was a negative outcome for not following the physician's order. During an interview on
12/10/2025 at 2:17 PM the DON reported that staff were not following the physician's order per the record.
The DON stated Resident #38's oxygen order should have been 2-4L/min rather than 4L/min. The DON
stated she had contacted the physician, and the order would be changed to reflect 2-4L/min. The DON
stated she and the floor nurses were responsible for ensuring correct dosages were administered and
acknowledged that because the physician's order stated 4L/min, the discrepancy would have been
addressed. The DON stated that failure to administer the correct oxygen dose could have resulted in harm
to the resident. Record review of the facility provided policy titled, Oxygen Administration updated April
2025, reflected the following: Purpose: The purpose of this procedure is to provide guidelines for safe
oxygen administration. Preparation: Verify that there is a physician's order for this procedure. Review the
physician's orders or facility protocol for oxygen administration.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676461
If continuation sheet
Page 5 of 6
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
676461
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Country View Living
701 Butler Blvd.
Dimmitt, TX 79027
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 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to store, prepare, distribute, and serve food in
accordance with the professional standards for food service safety for 1 of 1 kitchen reviewed for kitchen
sanitation. 1. The facility failed to ensure freezer items were properly stored, labeled, and dated. These
failures could place residents who ate food served by the kitchen at risk of food-borne illness. Findings
included: Observation of the freezer on 12/9/25 at 9:40 AM revealed the following:1. (2) plastic bags of okra,
no label or date, not in original box. 2. (3) plastic bags of frozen chicken strips, no label or date, not in
original box. Observation of the freezer on 12/10/25 at 11:00 am revealed the following: 1. (2) plastic bags
of okra, no label or date, not in original box. 2. (3) plastic bags of frozen chicken strips, no label or date, not
in original box. In an interview and a walk through with the DM on 12/10/25 at 11:20 AM, the DM stated she
expected the kitchen staff to label and date all food items as they were used or taken out of the box. The
DM stated she had done spot checks on a weekly basis. When asked who trained the staff on labeling and
dating foods, she stated she had trained the staff on labeling and dating the food. The DM stated the
consequences of not labeling and dating foods would be food borne illnesses could make residents sick.
Record Review of the policy titled Food Storage dated April 2021, documented: Food must be stored in
properly covered containers with a date and label identifying the food item. Foods may remain in the
[NAME] box as long as content and date are easily visible on the box. Any food removed from the [NAME]
box must be labeled and dated.
Event ID:
Facility ID:
676461
If continuation sheet
Page 6 of 6