Patient Safety Indicators1
Patient Safety Indicators1
INTRODUCTION
The Patient Safety Indicators (PSIs) are a set of 26 indicators (including 18 provider-
level indicators) developed by Agency for Healthcare Research and Quality (AHRQ) to
have information on safety-related adverse events occurring in hospitals following
operations, procedures, and childbirth.
LEVELS OF PSIs
PSI indicators are at two levels- area level PSIs and provider level PSIs as tabulated
here
Definition:
A vulnerable patient is unable to protect and take care of him or herself, against
significant harm or exploitation.
PREVENTION OF FALL
In order to assess the fall risk, tools used are discussed ahead. Morse fall risk
assessment is tabulated as follows:
Humpty dumpty scale for paediatrics (HDFS), is a seven- item assessment
scale developed to assess which is used to document gender, age, diagnosis,
environmental factors, response to surgery/sedation, cognitive impairments,
and medication usage.
Obstetric fall risk assessment tool uses a scoring system that determines the
female vulnerable patient's risk for a fall and provides a structured systematic
approach for RNs to use.
Care for prevention of fall: The following measures are taken in this regard:
Fall leaf is displayed on patient cot.
Restraints may be used to prevent fall of unconscious or mentally unstable
patients. Hospitals must have disabled-friendly environment as many
patients categorized as vulnerable may be disabled.
Such patients should be monitored more frequently for ensuring that they
are safe. They shall be accompanied by an attendant while going to
washroom or any other area.
The washroom must have grab bars, anti-skid mats and call alarm system.
While they are on bed, safety railings should be put up in place to prevent
fall from bed.
While being transported on wheelchairs or stretchers, safety belt shall be put
up
PREVENTION OF IATROGENIC INJURY
Up to 50% of adverse events that occur in hospitals are preventable, latrogenic
illnesses are most commonly associated with medications, diagnostic and
therapeutic procedures, nosocomial infections, and environmental hazards.
Healthcare practitioners ensure that the required services are provided, and
duplication of these services is also avoided too.
Drain is a tube used to remove pus, blood or other fluids from a wound. The drain is
fixed by a suture at the end of the wound and a safety pin must be placed through
the end to prevent the drain slipping inwards.
Replace fluid loss through drain by additional IVFs. Drains should be removed
once the drainage has stopped or becomes less than 25 mL/day. Drains can
be 'shortened by withdrawing approximately 2 cm per day, allowing the site
to heal gradually.
Drains that protect post-operative sites from leakage form a tract and are
usually kept in place for one week.
Emptied every 8 hours or as needed, mark and date the output every 8 hours.
Change when full or not working, record drainage in ostomy bag or number
of dressing changes if no bag is used.
? Hickman Catheter
Wash and disinfect your hands with 70% alcohol, wear PPE before entering
the patient's room (Isolation Room), disinfect your hands again.
Record chest tube output of past 24-hourperiod every morning, ensure that
clamp is open for drainage, consider removing chest tube once output is less
than 200 ml. in 24- hour-period.
Remove sutures around chest tube while holding chest tube steadily in place
Instruct patient to perform valsalva maneuver. Withdraw chest tube quickly
while simultaneously covering entrance site with Vaseline gauze.
Tightly tape 4 x 4 gauze over entire entrance site ensuring that no air is able
to leak into the chest tube wound.
Document chest tube removal.
Policy
Restraint may only be used to ensure the immediate physical safety of the patient,
staff or others and must be discontinued at the earliest possible time. Alternative and
nonphysical interventions are attempted prior to use of restraints. Patient's dignity
should be maintained during restraint.
Physician orders
✓ Restraints shall be applied with only a physician's order that defines the
reason for restraint, less restrictive alternatives attempted/considered, type
of restraint to be used, and duration for which the restraint may be applied.
✓ The time limit shall not exceed one calendar day, after which new orders are
required if restraints must be continued.
✓ In emergency situations, (ie., self-extubation), if the physician is not available
to issue the restraint order,
✓ restraint is initiated by a registered nurse based on an appropriate
assessment of the patient.
✓ In that case, the physician is notified within 12 hours of the initiation of
restraint and a written order is obtained from that physician and entered into
the patient's medical record.
Reassessment of use:
The Consultant, in collaboration with the health care team, shall evaluate the patient
at
The end of the prescribed duration of restraint to determine the need for
continued use
Of the device(s). If restraint remains necessary, the order must be renewed.
In the absence of order renewal, restraints shall be removed by the responsible
Nursing staff.
Reapplication of Restraint
The patient is continually assessed to ascertain his or her condition and to
determine if restraint can be discontinued.
If a patient, who was recently restrained, must be placed back into restraints, new
physician order is required.
A temporary release that occurs for the purpose of caring for a patient's needs
(e.g., toileting, feeding, and range of motion) is not considered a discontinuation of
the Intervention.
Circulation: The affected limb(s) has been checked and device application has been
determined not to impair circulation to the extremity:
• Nail bed blanched in less than 3 seconds
• Pulse is present above and below restraint.
Skin integrity: Skin integrity has been checked under and around the device(s), and
at all bony prominences and no pressure or reddened areas have developed.
• The patient is covered either by gown, sheet, or curtain and is protected from public
view.
• Device application: The device is applied according to the manufacturer's guidelines
and in a manner that is secure but not tight. Straps are secured to bed or chair frame
(never to side rails or other moveable parts); and quick release is possible.
• Fluid needs: Fluids are administered as ordered by the physician. If the patient is
not on fluid restriction, oral fluids are offered at least every two hours. If the patient
is nothing by-mouth (NPO), oral care is provided at least daily to maintain integrity of
oral mucosa.
• Toileting needs: Elimination needs are attended to, either by foley catheter (only if
ordered for other medical necessity) or by offering the patient the bed pan or
assistance to bathroom or bedside commode chair.
• Nutrition offered: Nutritional needs are met as ordered by the physician. If oral
intake is allowed, the patient is offered and assisted with meals and snacks.
• Range of motion: Active or passive range of motion in the affected limb(s) is
completed either by the patient or the caregiver. For patients requiring limb
restraints, ROM is recommended at least every 2 hours.
• Evaluation for restraint reduction or removal: Need for the use of restraint(s) is
evaluated frequently (at least every two hours) and restraints are discontinued at the
earliest possible time
Confirm the diagnosis of thalassemia and appropriate clinical and laboratory for
transfusion.
Use careful donor selection and screening, favouring voluntary, regular, non-
remunerated blood donors.
Before first transfusion, perform extended red cell antigen typing of patients at
least for C, E, and Kell.
At each transfusion, give ABO, Rh(D) compatible blood. Matching for C, E and Kell
antigen is highly recommended.
Before each transfusion, perform a full cross-match and screen for new antibodies,
or in centres that meet regulatory requirements, perform an electronic cross-match.
Use leucoreduced packed red cells. Pre-storage filtration is strongly recommended,
but blood bank pre-transfusion filtration is acceptable. Bedside filtration is only
acceptable if there is no capacity for pre-storage filtration or blood bank
pretransfusion filtration.
Use washed red cells for patients who have severe allergic reactions.
Transfuse red cells stored in CPD-A within one week of collection and red cells
stored in additive solutions within two weeks of collection.
Transfuse every 2-5 weeks, maintaining pre-transfusion haemoglobin above 9-10.5
g/dL. or higher levels (11-12 g/ dl.) for patients with cardiac complications.
Keep a record of red cell antibodies, transfusion reactions and annual transfusion
requirements for each patient.
Keep the post-transfusion hemoglobin below 14-15 g/dl.
METHODS OF TRANSFER
o For a single person (One first aiders) are - Drag method. ankle pull/leg pull
method, shoulder pull/collar pull method, blanket pull method, cradle
method, fireman’s carry, pick-a-back carry and human crunch method.
o For two persons (Two first aiders): Twohanded seat, double human crutch,
fourhanded seat, wheel chair method, chair method and stretchers
SURGICAL SAFETY
CARE COORDINATION EVENT RELATED TO MEDICATION
RECONCILIATION AND ADMINISTRATION
✓ Understand how three particular key drug classes correspond with many
ADEs: Anticoagulants (bleeding) opioids (accidental overdoses, sedation, and
respiratory depression) and diabetes agents (Hypoglycemia), Due as the high
risks of inaccurate or missing information, provides must have point of-care
access to comprehensive, real-time actionable pharmacy data to help ensure
more complete documentation and reduce ADEs in the process.
✓ Commit extra resources toward keeping certain high-risk populations, such
as the elderly and paediatric patients, safe.
Identifying the appropriate medication, dose, and frequency. Mistakes can often
occur in this point to the reconciliation process, often attributable to gaps in
information.
✓ Capture all medications and their details: While documenting the details of
a patient's prescription, medications is critical, also ask for information about
all other medications, such as vitamins, herbals, health supplements,
nutraceuticals, respiratory therapy-related medications (e.g.. inhalers),
vaccines, and intravenous solutions. Be sure to capture the medication name,
strength, dose, route, formulations, frequency, and most recent dose taken.
✓ Help patient recollect the memory: Patients who take multiple medications
can struggle to remember all of them. Probing questions can help with
memory recollection. Types of probing questions include open-ended
questions, close ended questions, and questions about specific conditions.
Providers must take health literacy into consideration when working on developing
an accurate medication list and educating patients on their regimen and potential
risks. Specifically, it can be helpful to target efforts on improving communication.
Listen: Put your thoughts on hold before responding and take time to understand the
perceptions of others.
Ensure that your entries in the EMR are accurate and complete: Prior to finalizing
your medical record entries. review them as diligently as you would an important
article or letter you might write.
Focus first on areas where risk is highest: The top two areas of vulnerability are
surgery and emergency departments. These two areas must be focused.