F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Immediate
jeopardy to resident health or
safety
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to implement respiratory care interventions including ensuring
the application of hand mitten restraint as ordered, and to maintain patency of trach tubes due to resident
history of chronic pulling of tracheostomy tube according to the plan of care for 1 of 3 (R4) residents
reviewed for tracheostomy care. As a result of the facility's noncompliance with mittens not being applied
and monitored by staff, R4 was able to reach her tracheostomy tubing and self-decannulated which led to
her expiring. Findings Include:Based on interview and record review, the facility failed to implement
respiratory care interventions including ensuring the application of hand mitten restraint as ordered, and to
maintain patency of trach tubes due to resident history of chronic pulling of tracheostomy tube according to
the plan of care for 1 of 3 (R4) residents reviewed for tracheostomy care. As a result of the facility's
noncompliance with mittens not being applied and monitored by staff, R4 was able to reach her
tracheostomy tubing and self-decannulated which led to her expiring.The Immediate Jeopardy began on
[DATE]. V1 (Administrator) was notified on [DATE] at 2:31 PM of the Immediate Jeopardy. The facility
presented an initial removal plan of [DATE]. The plan was accepted, and on [DATE] the surveyor conducted
an onsite record reviews and interviews to confirm the removal plan was implemented. V1 was informed the
Immediate Jeopardy was removed on [DATE].Although the immediacy was removed, the facility remains
out of compliance at severity level II until the facility can evaluate the effectiveness of the removal plan and
maintain substantial compliance with this regulation.R4 is a [AGE] year-old with the following diagnosis:
aphasia following cerebral infarction, acute respiratory failure with hypercapnia, tracheostomy status,
dependence on supplemental oxygen. R4 admitted on [DATE] and expired in the facility on [DATE].On
[DATE], R4 was found unresponsive with the tracheostomy pulled out and later pronounced expired in
facility by paramedics. On [DATE] at 9:44 AM, V1 (Administrator) and V2 (Assistant Director of Nursing)
informed surveyor that their electronic medical records (EMR) were down from [DATE] until the morning of
[DATE]. All clinical documents were produced manually during this time. However, a completed progress
note was not provided because it was not done as confirmed by V2. There was also no documented
incident report of [DATE] provided to the surveyor.A police report from [NAME] Hills Police Department was
obtained pertaining to the death incident of R4 on [DATE]. Report indicate V17 (Agency Nurse) informed V3
([NAME] Hills Police) that she was the nurse for R4. According to report on [DATE], between the times of
5:55AM and 6:05AM, V17 was in the room assisting another resident when V17 observed R4's trach tube
not in place and R4 was unresponsive. Police interview of V11 (Respiratory Therapist/RT) indicated that he
was the respiratory therapist of R4 and approximately at 4:45 AM of [DATE], V11 was in the room of R4
assisting with trach care. V11 stated R4 is supposed to wear glove restraints (identified as mittens) to
prevent her from removing her trach tube as she has history of removing her trach tube. Report indicated
that V11 stated he did not observe R4 wearing glove restraints while in the room. Report indicated an
Residents Affected - Few
(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 4
Event ID:
145650
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
145650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/02/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Nexus at Palos
10426 South Roberts
Palos Hills, IL 60465
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 - Immediate
jeopardy to resident health or
safety
Residents Affected - Few
interview with V16 (Nursing Supervisor) was also completed. V16 stated R4 was supposed to always wear
the glove restraints according care plan. V17 stated that it was her first time working with R4 and was
unaware that glove restraints were to be in place. Additionally, V17 reported that the facility online medical
records database of R4 for physician orders and plan of care were inaccessible and V17 was not provided
with updates, information or paperwork pertaining to R4 by the prior shift nurse. V16 informed V3 that there
should be a binder at nurse station with R4's plan of care information. Report indicated V3 checked the
binder and did not appear to be properly filled out.On [DATE] at 10:25AM, V3 ([NAME] Hills Police
Department) stated he arrived at facility with R4 unresponsive and 911 paramedics working on her. Staff
were interviewed and nurse on duty/ Agency nurse told V3 at approximately 5:55A - 6:05A R4 was
observed with trach not in place (pulled out). V3 said while in the facility he did not observe R4's mittens in
placed. V3 said employee informed him that electronic access to chart was down from a week to a week
and half. V17 stated she did not get report from outgoing nurse regarding R4's mitten needs to be in placed
at all times and V17 has no knowledge of facility restraint policy. V3 stated he believed there was neglect on
facility as staff do not know their restraint policy and there was no hand off report from nurse to nurse
according to his interview with agency nurse who was on duty.On [DATE] at 11AM, in separate interviews,
V2 and V4 (Restorative Nurse) both stated R4 should have mittens on at all times to maintain trach patency
because R4 has a history of pulling on trach tubes.On [DATE] at 10:28AM, V7 (Attending Physician/AP),
stated he is the AP in facility only and not R4's community doctor. V7 said the last time R4 was seen was
Friday, [DATE]. R4 was stable. He was aware that R4 has history of pulling on trach tube and the plan was
to apply restraint (mitten) to prevent R4 from pulling trach. There was an order for mittens to be on at all
times, staff to monitor, and may remove only when there is staff present and working with resident. V7
signed off on the Death certificate with cause of death, Respiratory Failure (not complete list). V7 stated the
immediate cause of death was possibly R4's trach being pulled out since there was no oxygen being
received by R4.On [DATE] at 11:34 AM, V8 (Certified Nursing Assistant/CNA) stated she work 11-7 shift on
8/23 thru 8/24 and was assigned to R4. V8 said she rounded on R4 every 2 hours and at 5:00AM she
provided incontinence care. V8 said she did not visibly saw the mittens being on during her entire shift. V8
said no one communicated to her about R4's need of mittens. V8 stated she do not know the facility
restraint policy and only received education today in the morning. V8 further state that during police
investigation and interview with staff she was present and heard the nurse did not know anything about R4
needing mittens. V8 said there is no CNA to CNA shift to shift report or endorsement.On [DATE] at 1:42
PM, V11 (Respiratory Therapist/RT) stated he was the RT working with R4 on 8/23 -[DATE]. V11's shift is
7p - 7a. On [DATE] at 6:15AM nurse called stated R4 trach was out. When he went to the room V11 said R4
did not look like she was breathing and there was no pulse. V11 stated he do not re-call seeing R4's mittens
on. V11 said there was an order for mittens as R4 have the history of self-decannulating behavior. V11
rounded 6X on R4 during his shift and at one point he reported to the nurse that mitten needs to be
applied, however, V11 said he was unsure if nurse went to the room to check after acknowledging he was
heard.On [DATE] at 10:25 AM, V14 (R14's Daughter) stated the incident of her mother pulling on
tracheostomy tube occurred 3x since admission to facility. Stated facility was aware before admission that
her mother was on restraints from another facility because of behavior. Requested for restraint but was told
initially by V13 (Regional Nurse Consultant/ Interim DON) that facility is restraint free and that they do not
use restraint in the building, but later it was decided that R4 needed it after the 2nd attempt and upon return
from hospital. During this investigation, multiple call attempts to V17 (Agency Nurse) for an
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145650
If continuation sheet
Page 2 of 4
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
145650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/02/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Nexus at Palos
10426 South Roberts
Palos Hills, IL 60465
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 - Immediate
jeopardy to resident health or
safety
Residents Affected - Few
interview was done with no success of a call back.Review of R4's medical records indicate an admission
date of [DATE] with diagnosis information of aphasia following cerebral infarction, tracheostomy status and
dependence on supplemental oxygen (not a complete list). Comprehensive assessment of MDS Section O,
dated [DATE], indicated R4 with tracheostomy care, Section C, [DATE], indicated Brief Interview for Mental
Status (BIMS) was not conducted. Order Summary Report, start date [DATE], read: Monitor left hand mitt
for circulation, motion, sensation, PAIN, ROM. Every 2 hours for monitoring remove mitt for 10-15 period,
CMS/ADL/ROM. Care Plan Report, date initiated [DATE] read: Focus- Physical Restraints: Requires
physical restraint r/t pulling on mechanical equipment. Interventions include Check and remove restraints as
per policy. Keep resident close to areas that are supervised. Provide hazard free environment. Special
Instructions read: Apply MITT to LEFT hand to maintain patency of trach tubes due to patient chronic
pulling of tubing. Ventilator/Aerosol Flowsheet indicated Trach care was done by V11 on [DATE] at 8:30 PM
where trach inner cannula was changed. Consent for Use of Restraint/Device, effective date [DATE] read: 2.
Benefits, a. Based on the resident's individual needs, restraints may be beneficial for the following. 2.
Prevention of injury to self or other. Progress Notes, Effective Date: [DATE] 15:39 Type: Nurses Notes: Note
Text: @ 0910 Pt., was observed by this nurse with her trach out, immediately RT was called to pt's room by
CNA. 2 RT put the trach back in and SPO2 97 HR 66. Progress Notes, Effective Date: [DATE] 23:59 Type:
Nurses Notes: Note Text: A Shiley 5XLTD decannulation occurred. Nurse notified the RT. Despite multiple
attempts, the trach wouldn't reinsert. DON was notified. RT applied a 4x4 gauze over the stoma and a
non-rebreather mask. R4 was stable at 95% oxygen saturation and 82 b/m HR. Ambulance left with her not
in distress. Progress Note, Effective date [DATE] 20:08 Type: Nurses Notes: Note Text: Writer called resident
daughter to inquire / inform of the use of hand restrain, daughter verbalized that she is aware of such order
from the hospital and gave verbal Consent for the use of the hand mitten to restrain resident from pulling
out her trach again. Nurse on Duty made aware. Facility did not provide progress note or completed
incident report for [DATE] self-decannulation incident. Review of Illinois Certificate of Death read Cause of
Death, Immediate Cause a. Nontraumatic Intracerebral Hemorrhage, b. Acute Respiratory Failure, c. Type 2
Diabetes. Certificate was signed and certified by the Attending Physician/Physician in Charge on [DATE].
Policy and ProcedureGuideline: Physical Restraint/Device, Review date 10/2021General: To provide
guidance on the assessment for the use and documentation of physical devices including, but not limited to,
position change alarms, bed rails, furniture positioning, concave mattress, reclining chairs, cushions such
as wedge shaped, hand mitts, abdominal binders, etc. A physical restraint is any manual method, physical
or mechanical device/equipment or material that limits a resident's freedom of movement and cannot be
removed by the resident in the same manner as it was applied by staff.Guideline:2. If is determined that the
physical device is a restraint: a. A physician order will be obtained. b. Education will be provided to the
resident/resident representative regarding the risks and benefits of the physical device. c. Informed consent
will obtain from the resident/resident representative using the Consent for use of Restraint/Device Form3. If
a resident or resident representative request the use of a restraint, then the facility will evaluate the
appropriateness of the request and consult with the physician/NP to determine if resident has a medically
necessary reason for the restraint.6. the effectiveness of physical device in treating the medical symptoms
or as a therapeutic intervention and any negative impact on the resident shall be assessed by the facility
throughout the period of time the physical device is being used and documented in the progress note.7. The
behavior incident that prompted the use of the physical device will be documented in the progress note.8.
The date and time the physical device was applied and released will be
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145650
If continuation sheet
Page 3 of 4
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
145650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/02/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Nexus at Palos
10426 South Roberts
Palos Hills, IL 60465
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 - Immediate
jeopardy to resident health or
safety
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
documented in the progress note.9. the name and title of the person responsible for the application and
supervision of the physical device will be documented in the progress note. On [DATE] the surveyor verified
by interview and record review that the facility implemented the following to remove the
immediacy:Immediate Actions:The facility took the following actions to address the citation and prevent any
additional residents from suffering an adverse outcome. All residents with tracheostomies were reviewed by
DON/Unit managers. Completed on [DATE]. The review was done to ensure special instructions which
includes mittens or other physical restraints were in place per physician orders and resident care plans.
There was one resident to was identified with a physical restraint. No other concern was identified related to
use of physical restraints during the review.The DON/Unit Managers provided education to nursing staff
(nurses and nursing assistants), RT's (respiratory therapists) including Agency staff on special instructions
such as use/application of mittens and other physical restraints for residents with Tracheostomy, following
care plans and physician orders. Completion date: [DATE].The DON/Nurse Managers provided education to
the nurses, including nurse agency staff, on change of shift reporting. The training also included notifying
nursing assistants of any new special instructions at the start of the shifts. Completion date: [DATE].All
nursing staff (nurses and nursing assistants) and RT's (respiratory therapists), including agency staff, who
are not available and/or currently on vacation will also receive the same education upon their return to
work. The DON/Unit Managers will provide the same training. Ongoing. Additional Interventions:The
DON/Unit Managers will continue to audit new admissions with Tracheostomy to ensure that orders for
physical restraints are care planned and are communicated with the nursing staff and RT's. Initiated on
[DATE].The DON, Administrator, Unit Managers reviewed the policies and procedures related to physical
restraints, tracheostomy, nursing rounds, care plan and following physician orders. There is no revision
necessary. Completion date: [DATE].The QAPI committee held an Ad-Hoc QAPI meeting to discuss R4,
and action actions described in this plan of removal. Completion date: [DATE].The DON/Unit Managers will
conduct audit and observation of all residents with tracheostomy weekly for four (4) weeks to ensure
compliance with special instructions, such use if mittens and physical restraints are being implemented,
physician orders and care plan interventions are followed. Ongoing.The results of the audit/observation will
be reviewed by the QAPI committee weekly for four (4) weeks. The QAPI committee will determine if
additional corrective actions are necessary to maintain compliance. Ongoing.The facility asserts the
likelihood for serious harm no longer exists on [DATE].
Event ID:
Facility ID:
145650
If continuation sheet
Page 4 of 4