Unit 5.5 - JCI
Unit 5.5 - JCI
Unit 5.5 - JCI
International
JOINT COMMISSION
INTERNATIONAL
Joint Commission International (JCI) is a
division of Joint Commission Resources (JCR),
the subsidiary of the Joint Commission on
Accreditation of Healthcare Organizations
(JCAHO). Its mission is to continuously
improve the safety and quality of care in the
international community through the
provision of education and consultation
services and international accreditation.
Evolution of the Joint Commission
• 1910 – 1913: Concern for the quality of hospital care in the U.S.
• 1910: Ernest A. Codman, M.D., focused on results & outcomes of
treatment.
• 1918: American College of Surgeons began Hospital Standardization
Program.
• 1951: Joint Commission on Accreditation of Hospitals (JCAH) formed
to continue the challenge.
• 1965: Social Security Act Ammendments added credibility to the
JCAH’s functions.
• 1987: JCAH renamed as Joint commission for Accreditation of
Healthcare Organisations (JCAHO) to widen the scope
• 1999: Joint Commission International (JCI) launched International
Accreditation Programmes.
JCI Accreditation
According to JCI, accreditation is a process in which an entity, separate
and distinct from the health care organization, usually non-
governmental, assesses the health care organization to determine if it
meets a set of standards designed to improve quality of care.
Accreditation is usually voluntary and standards are usually regarded
as optimal and achievable. Accreditation also provides a visible
commitment by an organization to improve the quality of patient care,
to ensure a safe environment and to continually work to reduce risks to
patients and staff.
The standards will be revised and published at least every three years.
Accreditation Surveys
• interview with staff and patients and other verbal information;
• on-site observations of patient care processes by surveyors;
• policies, procedures, clinical practice guidelines, and other documents
provided by the organization
Patient-Centered Standards
The organization supports the patient’s right to respectful and compassionate care at the end of life.
• Patient informed consent is obtained
• The organization informs patients and families about how to gain access to clinical research, clinical
investigation, or clinical trials involving human subjects.
• Informed consent is obtained before a patient participates in clinical research, clinical investigation, and
clinical trials.
Assessment of Patients (AOP)
• Each patient’s initial assessment(s) includes an evaluation of physical,
psychological, social, and economic factors, including a physical
examination and health history.
• Assessment findings are documented in the patient’s record and
readily available to those responsible for the patient’s care.
• All patients are reassessed at intervals based on their condition and
treatment to determine their response to treatment and to plan for
continued treatment or discharge.
• Qualified individuals conduct the assessments and reassessments.
Laboratory Services
• All equipment used for laboratory testing is regularly inspected, maintained, and
calibrated, and appropriate records are maintained for these activities.
• Procedures for collecting, identifying, handling, safely transporting, and disposing
of specimens are followed.
• A laboratory safety program is in place, followed, and documented.