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JCAHO
Patient Safety Goal
Gerard X. Brogan Jr., MD FACEP Section I: Patient 's Identification A: What is the procedure for initially identifying a patient in the Emergency Department? Upon presentation to Triage, patients will receive an arm band that has the patient's name and date of birth. The patient's room number or bed position must not be used as an identifier. B: What identifiers do you use? Patients shall be identified using a minimum of 2 patient identifiers which will include patient's name and patient's date of birth. The patient's medical record number may be used as a 3rd patient identifier, if necessary. The patient's room number or bed position must not be used as an identifier. Prior to placement of identification data, a designated individual will ask the patient to state and spell his/her full name and his/her date of birth. If the patient's identifying band is removed or missing during hospitalization, the patient must be re-identified as described above prior to placement of new identification band. C: How do you identify an unresponsive patient? If a patient is unable to provide information for any reason, a designated individual will ask the family member, guardian, significant other or appropriate individual to state, spell the patient's full name and provide date of birth, if known, and confirm the patient's full name and date of birth on the patient's identification band as accurate. If the patient is unable to provide information and there is no family member, significant other or accompanying individual available, a designated individual will identify the patient as Jane/John Doe and use the admission date in place of a date of birth. D: How do you identify a nursing home patient? An identification band from the Emergency Department or other health care facility must be removed and replaced with a new identification band once the patient is admitted as an in-patient. Patient's arriving from a nursing home will be identified both by the patient's arm band with confirmation of the patient's transfer papers and medical record. In addition, the above procedures for identifying the patient will be utilized, including asking the patient for their name and date of birth. If the patient is unable to provide the information for any reason, a designated individual will ask the paramedic regarding significant other or accompanying individual to state and spell the patient's full name and provide the date of birth if known, and confirm that the patient's full name and date of birth on the identification band is accurate. E: What is the procedure prior to medication, registration, diagnostic testing or basic procedure? Prior to the patient receiving any treatments or procedures, any transportation, specimen collection, receiving medications, the administration of blood products, hospital personnel must identify the patient by asking the patient to state his/her full name and date of birth and verify by matching identifiers on the identification band, with the information on the appropriate requisition. Section II: Communication Among Caregivers A: How do you provide for coordination among the health professionals and services or settings involved in patient care? Describe the processes for referral, transfer or discharge of patient to another level of care. Coordination of care is accomplished by both clear and complete notes in the medical record as well as clear sign-outs and transfer reports from the Emergency Department to the floor and from shift-to-shift in the in-patient setting. When patients transfer from one unit to another, a new set of transfer orders and a transfer note is competed, in addition to verbal report from the sending unit to the receiving unit. Upon discharge there are written discharge instructions, in addition to verbal report to either the family or to the receiving institution (i.e. nursing home) is completed. B: How do you provide for the change of appropriate patient care and clinical information when patients are admitted, referred, transferred or discharged? When patients are admitted, referred, transferred or discharged, a written record is exchanged with the receiving facility, as well as a verbal report given. C: Do you have a list of abbreviations that are not to be used? Yes. The do not use abbreviations include:
D: What do you do when an order contains an abbreviation that is prohibited? If a healthcare provider receives an order using an abbreviation on the "do not use" list that order must be clarified with the ordering practitioner. If confirming this order delays treatment or puts the patient at risk, and the order is clear and complete, than the order should be carried out and the confirmation obtained as soon as possible thereafter. (Please note that System-wide, the qd, µ, µ.g abbreviations are not to be used.) In addition, individual facilities have selected other Do Not Use abbreviations as described above. E: What is the process for taking verbal or telephone orders and receiving reports of critical test results? A verbal order may only be issued in an emergency when a clinician is unable to document such an order personally due to the condition of the patient or the emergent nature of the situation. The following clinicians may issue a verbal inpatient order: The attending physician, dentist, podiatrist, physician assistant, nurse practitioner, nurse midwife, house staff and certified registered nurse anesthetist. Recipients of a verbal inpatient order may include a registered nurse, a licensed practical nurse, a registered therapist, a licensed, certified respiratory therapist and a licensed technologist within the scope of their practice. In an emergency situation, such as a code or in the operating room, a clinician may communicate a verbal order. The recipient must repeat back the order, clinical receive confirmation of the accuracy before administering the order. The clinician must sign the verbal order immediately following the completion of the emergent situation and/or scheduled procedure. No verbal or telephone orders may be issued for therapeutic agents or total parenteral nutrition. Verbal orders for laboratory testing must be followed up with a hard copy of the test requisition, as per Federal and State requirements. With respect to telephone orders, the process is as follows: The clinician first issues a telephone order. The recipient documents the order on the physician order sheet and the patient's medical record. Documentation includes a purpose or indication of the order, if applicable, the drug name, dose, route, frequency and duration and the date and time the order was received by the clinician. The recipient then reads back the order to the clinician verbatim with each numerical digit articulated individually. Confirmation of the read-back from the clinician must be documented on the order sheet. The recipient then signs the order. For orders written on more than 1 page, there should be documentation of the read-back confirmation on each page. The clinician must sign the order within 48 hours after the order was issued. For telephone reporting of critical test results, test result accuracy must be verified by the person receiving the order, reading back the complete test results. F: Do you have established time frames for reporting critical test results to the care provider and are they being met? Yes. Critical test results are reported immediately to the care provider. This is documented in the lab information system by the lab technologist placing the call. including the person and time that the lab was spoke with them. This procedure is monitored by the laboratory. Section III: Medication Safety A: Do you have standardized drugs/IV concentrations? Concentrated electrolytes have been removed from patient care units, including but not limited to potassium chloride, potassium phosphate and sodium chloride greater than 0.9%. In addition, we have standardized and limited the number of drug concentrations available within the Health System. Patient care providers have been educated on high-risk, high-alert medications and ongoing monitoring will be conducted through the medication error in the reporting process. Each site will establish a process for pediatric review of its high-risk/high-alert verification and associated safety processes. Section IV: Eliminate Wrong Site, Wrong Patient, Wrong Procedure, Wrong Surgery A: Describe the process for patient/ site, procedure verification procedure prior to performance of an invasive procedure. For all procedures (in or out of the OR) involving right, left, distinction, multiple structures, such as fingers and toes or multiple levels such as spinal procedures, the intended site must be marked so that the mark will be visible after the patient has prepped and draped. Exceptions to this include single organ cases, interventional cases for which a catheter or instrument insertion at site has not been determined, premature infants, teeth (but indicate the operative tooth names on documentation or mark the operative tooth on the dental radiographs or dental diagrams), or for bedside procedure cases, in which the individual doing the procedure is in continuous attendance with the patient from the time of the decision to do the procedure and consent from the patient to the conduct of the procedure. Specific guidelines include that the person performing the procedure will mark the site prior to moving the patient into the room where the procedure will be done. The site marking will take place before the patient is sedated so that the patient can participate in the procedure. Following proper patient identification, the site will be marked by the person who will be performing the procedure with participation and verification by the patient, if the patient has the capacity. The site must be marked at or near the incision site. Every procedure will be marked in the same manner (an x may not be used). The mark should be made with a marker that is sufficiently permanent to remain visible after completion of the skin prep (stickers may not be used). The mark should be positioned to be visible after the patient is prepped and draped. Verification of the site mark will take place during the timeout. Section V: Infusion Pumps A: Are your infusion pumps protected against free flow? To improve the safety of infusion pumps, free-flow protection on all general use and PCA intravenous pumps is in place. Each facility will conduct an inventory to determine the type and number of infusion pumps used. All new equipment will be inspected by the biomedical engineering department to ensure that it is free flow protected. Section VI: Clinical Alarms A: What kind of alarms do you have in the department? Clinical alarm systems include alarms that are intended to protect patients and to alert staff of a risk or patient need. Examples include, but are not limited to, physiological monitor alarms, infusion pump alarms, ventilator alarms, infant security alarms, nurses call system alarms and patient monitoring alarms. The responsibility of the users to insure that the alarms systems are used appropriately and safely, and that sound levels are sufficient to notify staff in the event of an alarm. Patients and families will be educated regarding not tampering with or changing alarm settings. Section VII: Risk of Procedure for Responding to an Alarm Any staff member aware of an alarm sounding must respond. If the staff member is competent to address the clinical situation that staff member will do just that. If that staff member is not competent to address the clinical situation, that staff member will insure that an appropriate person is notified and does respond. A: What do you do when you hear an alarm sound? Upon hearing an alarm sound, the healthcare provider must respond to the patient. That healthcare provider is not appropriate to respond to a clinical situation the healthcare provider will immediately identify a healthcare provider competent in managing the clinical scenario and insure that that person comes to the bedside. Alarms will not be turned off/muted or otherwise changed. Section VIII: Reduce Infections A: What infection control procedures do you follow in evaluating patients? Healthcare practitioners will comply with current CDC hand hygiene guidelines. In addition, any cases of unanticipated death or major permanent loss of function associated with loss of function associated with healthcare associated infection will be managed as a sentinel event. B: Describe indications for using gloves. Universal precautions should be utilized for all patients. Gloves should be utilized for each individual patient and discarded prior to leaving the room. C: Describe the various types of isolation, in the cases the protective garments for each. PRINCIPLES OF ISOLATION: There are two (2) tiers of precautions: I. Standard Precautions
II. Transmission - Based Precautions:
STANDARD PRECAUTIONS
II. Standard Precautions are designed
to reduce the risk of transmission of microorganisms from both recognized
and unrecognized sources of infection in hospitals.
Hand Washing - the single most important measure to reduce the risks of transmitting microorganisms from one person to another. placement. Alcohol gel is appropriate for hand antisepsis before and after patient care, except when hands are visibly soiled 1. Gloves
2. Masks, Eye Protection, Face Shields
3. Gowns
4. Patient Care Equipment
5. Environmental Control
6. Linen
7. Occupational Health & Bloodborne Pathogens
8. Patient Placement - applies to patients that are hospitalized.
AIRBORNE PRECAUTIONS I. Patients Placement - applies to
hospitalized patients.
II. Respiratory Protection DROPLET PRECAUTION I. Patients Placement- applies to hospitalized patients.
II. Mask CONTACT PRECAUTIONS I. Patients Placement - applies to hospitalized patients. Patients in psychiatric settings and ambulatory settings, do not require Contact Precautions, Standard Precautions is adequate. Contact Precautions in the psychiatric and ambulatory settings shall be used only in an outbreak situation and as directed by Infection Control.
II. Gloves and Hand Washing
III. Gown
IV. Patient Transport
V. Patient Care Equipment
IMMUNOCOMPROMISED PATIENTS The use of Standard Precautions for all patients and Transmission - Based Precautions for specified patients, as recommended by the CDC Guidelines, should reduce the acquisition by these patients of institutionally acquired bacterial from other patients and environments. A: Describe the process for putting on and removing protective garments. Protective garments will be placed prior to entering the room. In addition, protective garments should be discarded of prior to exiting the room. Garments shall be discarded in such a way that the healthcare practitioner does not increase the risk self-contamination. Section VIII: Reconcile medications across the continuum of care. A complete list of the patient's current medications upon the patient's admission to the healthcare facility will be obtained and documented with involvement of the patient and their family. The process includes a comparison of the medications the healthcare system provides to those on the list. A complete list of the patients medications is communicated to the next provider of service, when it refers or transfers a patient to another setting, service, practitioner or level of care within our outside the organization. Section IX: A: Describe the process of evaluating the patients risk of falls and fall prevention technique. Each patient will be assessed and periodically reassess for risk of falling, including the potential risk associated with the patient's medication regimen and take action to address any identified risks. A risk assessment tool (i.e. Morse scale) may be used to identify patients at risk. After clinical assessment, if the clinical presentation warrants, the nurse may institute a high-risk fall protocol for those patients who do not meet the scoring criteria, according to the Morse scale. Implementation of fall prevention protocols and interventions will be based on the initial assessment. Risk factors include, but are not limited to, history of fall, medication use and alteration of mental status, unsteady gait, balance problems, weakness, visual impairment, ambulation device, advanced age, desire for autonomy, post op/post sedation or urgency/incontinence. An ongoing assessment of the environment will include the following key elements: floors, lighting, equipment, furnishing, toilet, bath facilities, corridors. Identified risk factors will be addressed immediately. Environmental rounds will be conducted at least monthly. In addition, the staff will be educated regarding fall prevention and injury reduction in new employee orientation, as well as on-going educational and annual competency. All patients or residents were assessed as at risk for falls will have an individualized fall prevention plan of care to reduce the occurrence of falls and/or injury and promote safety. The plan will be made in conjunction with the patient and it will include the identified risk factors as well as the interventions, such as lowering the bed and providing ambulation device. There will be continual reassessment and in addition, there will be patient and family education regarding fall prevention.
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