F 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, medical record review, staff interview, facility policy review, and review of
manufacturer instructions, the facility failed to ensure insulin was administered as ordered. This affected
one (#31) of seven residents observed for medication administration. The facility census was 38.
Residents Affected - Few
Findings include:
Review of the medical record for Resident #31 revealed an admission date of 07/24/23. Diagnoses included
type II diabetes mellitus, hypertension, hypothyroidism, chronic obstructive pulmonary disease, obstructive
sleep apnea, peripheral vascular disease, encephalopathy, major depressive disorder, and insomnia.
Review of the current physician orders for Resident #31 revealed an order dated 04/05/23 for blood glucose
levels to be obtained prior to meals with Novolog insulin administered subcutaneously (SQ) per sliding
scale via a Flex Touch pen. The order for insulin to be given per sliding scale was for blood glucose levels
between 140 milligrams per deciliter (mg/dL) and 199 mg/dL, inject two units of insulin; for blood glucose
levels between 200 mg/dL and 249 mg/dL, inject four units of insulin; for blood glucose levels between 250
mg/dL and 299 mg/dL, inject six units of insulin; for blood glucose levels between 300 mg/dL and 349
mg/dL, inject eight units of insulin; for blood glucose levels between 350 mg/dL and 399 mg/dL, inject 10
units of insulin; and for blood glucose levels greater than 400 mg/dL the physician was to be notified.
Observation on 08/07/23 at 11:59 A.M. revealed Licensed Practical Nurse (LPN) #500 obtained Resident
#31's blood glucose level and determined the level to be 171 mg/dL.
Continued observation of LPN #500 revealed the nurse returned to the medication administration cart, and
at 12:00 P.M., LPN #500 removed a clear plastic bag that contained the insulin pen (Novolog Flex Touch)
for Resident #31 from the medication cart. LPN #500 then removed a needle and two alcohol swabs from
the medication cart. The insulin pen was then removed from the bag, the cap was removed from the pen
and laid on the plastic bag from which the Novolog Flex Touch pen was removed. LPN #500 proceeded to
open an alcohol wipe, swabbed the top of the insulin pen, attached the needle, and dialed pen to two units
of insulin. While holding the insulin pen in the left hand, LPN #500 used the right hand to return the plastic
bag and the cap to the pen back into the medication cart. LPN #500 then locked the medication cart, picked
up the second alcohol swab, and entered Resident #31's room. LPN #500 approached Resident #31 and
injected the insulin into Resident #31's left arm.
Interview with LPN #500 on 08/07/23 at 12:02 P.M. confirmed the insulin pen was not primed when the
needle was applied and before administering insulin to Resident #31. LPN #500 stated insulin pens
(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 2
Event ID:
365571
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
365571
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/07/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Otterbein Portage Valley
20311 Pemberville Rd
Pemberville, OH 43450
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 0760
Level of Harm - Minimal harm
or potential for actual harm
do not require priming the needle when the needle was applied, and to just dial the pen to the ordered dose
and administer the insulin.
Interview with the Executive Director on 08/07/23 at 2:00 P.M. verified the Novolog Flex Touch pen was
required to be primed when the needle was attached to the pen.
Residents Affected - Few
Review of a policy titled, Insulin Administration, dated 06/21/17, revealed there are several insulin devices
on the market, and it is essential for the nurse to be familiar with the device prescribed and to always follow
manufacturers recommendations and when using pen devices, check the manufacturer's instructions prior
to use as many pens require priming or an air shot prior to administration.
Review of the manufacturers instructions dated March 2023 revealed the Novolog Flex Touch pen required
priming of two units of insulin to ensure insulin comes out of the needle tip to ensure the pen was working
correctly, and to remove all air bubbles to ensure the correct dose of insulin was provided.
This deficiency represents non-compliance investigated under Complaint Number OH00144886.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365571
If continuation sheet
Page 2 of 2