Patient Safety Improvement Act of 2016
A BILL
To reduce health care-associated infections and improve antibiotic stewardship through enhanced data collection and reporting, the implementation of State-based quality improvement efforts, and improvements in provider education in patient safety, and for other purposes.
2. Findings
3. Improving data reliability and surveillance
“938. Health care-associated infections and antibiotic use
“(a) GAO study on data validation strategies
“(1) In general—Not later than 1 year after the date of enactment of this section, the Comptroller General of the United States shall conduct an independent evaluation, and submit to the appropriate committees of Congress a report, concerning the action that the Centers for Disease Control and Prevention and State and local departments of health have taken to improve the completeness and accuracy of hospital-reported National Healthcare Safety Network surveillance data.
“(2) Content—The report submitted under paragraph (1) shall review and assess—
“(A) the types of external and internal data validation strategies that are conducted by the Centers for Disease Control and Prevention, State and local departments of health, and hospitals;
“(B) the frequency with which the Centers for Disease Control and Prevention, State and local departments of health, and hospitals audit data submitted to the National Healthcare Safety Network; and
“(C) identify additional actions that the Federal Government can take to support State and local departments of health and hospitals with such validation efforts and improvements to the quality of data submitted to the National Healthcare Safety Network.
“(b) Data reliability framework
“(1) In general—Following the submission of the report under subsection (a), the Director of the Centers for Disease Control and Prevention, in collaboration with the Administrator of the Agency for Healthcare Research and Quality and relevant stakeholders, shall develop a framework to improve the consistency and reliability of hospital data on health care-associated infections that is submitted to the National Healthcare Safety Network.
“(2) Requirements—The framework developed under paragraph (1) shall—
“(A) address issues identified in the findings of the study conducted under subsection (a);
“(B) propose data validation and reliability methodologies; and
“(C) assess the effectiveness and the cost to implement proposed methodologies.
“(c) Data collection pilot program
“(1) In general—The Administrator of the Agency for Healthcare Research and Quality, in collaboration with the Director of the Centers for Disease Control and Prevention, shall convene a meeting with relevant stakeholders to identify best practices and approaches for the collection and reporting of data on the incidence of health care-associated infections to the National Healthcare Safety Network by long-term care facilities, ambulatory surgical centers, and dialysis facilities.
“(2) Pilot program—After conducting the meeting under paragraph (1), the Administrator of the Agency shall establish and implement a pilot program to test best practices and approaches for the collection and reporting of data on the incidence of health care-associated infections by long-term care facilities, ambulatory surgical centers, and dialysis facilities. Such pilot program should incorporate applicable data validation methodologies and other recommendations described in the framework developed under subsection (b).
“(3) Report—Not later than 1 year after the completion of the pilot program under paragraph (2), the Administrator shall submit to the Secretary and the appropriate committees of Congress a report on the best practices identified through the pilot program under paragraph (1), including the lessons learned and challenges encountered with respect to data collection and reporting in long-term care settings, ambulatory surgical centers, and dialysis facilities as well as recommended data validation methods for those settings.
“(4) Authorization of appropriations—There is authorized to be appropriated, such sums as may be necessary to carry out this subsection. Amounts appropriated under the preceding sentence may be used for the purchase of software and technology that supports data collection and reporting.”
4. Aligning quality measures
5. Reducing the incidence of health care-associated infections
“320B. Efforts to reduce health care-associated infections
“(a) Grant program To reduce health care-Associated infections
“(1) In general—The Secretary shall award competitive grants to eligible entities to support State-based collaboratives in implementing evidence-based, regional approaches to infection prevention, control, and surveillance.
“(2) Purpose—Amounts awarded under grants under paragraph (1) may be used to support the following activities:
“(A) Inter-professional and inter-facility learning activities.
“(B) Building Statewide learning collaboratives.
“(C) Assisting with the implementation of the transition-of-care documentation required in section 5 of the Patient Safety Improvement Act of 2016.
“(D) Conducting a needs assessment to identify gaps in health care-associated infection prevention and reporting in a State or region.
“(E) Other activities determined appropriate by the Secretary.
“(3) Eligibility—To be eligible to receive a grant under this subsection, an entity shall be a public or private nonprofit entity that submits to the Secretary an application at such time, in such manner, and containing such information as the Secretary may require, including—
“(A) a description of the activities to be carried out under the grant, including the participants in any collaborative established to carry out such activities;
“(B) goals for the reduction in regional or Statewide rates of health care-associated infections;
“(C) an assurance that the entity will publicly report performance on a set of quality and outcomes measures determined by the Secretary; and
“(D) any other information determined appropriate by the Secretary.
“(4) Priority—In awarding grants under this subsection, the Secretary shall prioritize applicants that collaborate with multiple stakeholders across a region or State.
“(5) Authorization of appropriations—There is authorized to be appropriated, such sums as may be necessary to carry out this subsection.”
“(Z) to comply with the requirement of paragraph (4) (relating to the transmission of information regarding infections).”
“(4)
“(A) For purposes of paragraph (1)(Z), the requirement of this paragraph is that a hospital transmit information about infections or colonizations that present in an individual receiving treatment not later than 24 hours upon receipt of the culture to—
“(i) the individual;
“(ii) in the case of an individual who is being transferred to another provider, the receiving provider; and
“(iii) the individual's primary care provider, if identified.
“(B) The information described in subparagraph (A) shall contain the information fields included in the Centers for Disease Control and Prevention’s Inter-facility Infection Control Transfer Form and any other information the Secretary determines appropriate.
“(C) When transmitting information to a receiving provider under subparagraph (A)(ii), a provider shall, where practical, transmit such information electronically.”
“(82) in the case of any hospital (as defined in section 1861(e)) that is a participating provider under the State plan, provide that such hospital meet the requirements of subparagraph (Z) of section 1866(a)(1).”
6. Strengthening antibiotic stewardship
“(b) Grant program for State antibiotic stewardship action plans
“(1) In general—The Secretary, acting through the Director of the Centers for Disease Control and Prevention, shall award grants to States for the development of State plans to promote antibiotic stewardship and prevent the spread of antimicrobial-resistant bacteria across health care settings.
“(2) Eligibility—To be eligible to receive a grant under this subsection, a State shall submit to the Secretary an application at such time, in such manner, and containing such information as the Secretary may require, including—
“(A) an assurance that development of the plan under the grant will be led by an infectious-disease trained physician or a pharmacist with expertise in infectious disease; and
“(B) an assurance that the plan will focus on collaboration across acute and ambulatory care settings and include a summary of resource gaps and challenges.
“(3) Authorization of appropriations—There is authorized to be appropriated, such sums as may be necessary to carry out this subsection.”
“(c) Information Related to Antibiotic Use and Antimicrobial Resistance
“(1) In general—The Director of the Centers for Disease Control and Prevention shall annually prepare and issue a report concerning the aggregate national and regional trends of antibiotic use and bacterial resistance in humans to antibacterial drugs, including the identity of the 10 States with the highest number of prescriptions for antibiotics.
“(2) Stewardship workshops
“(A) In general—Beginning on January 1, 2019, and annually thereafter, the Director of the Centers for Disease Control and Prevention shall conduct at least one antibiotic stewardship workshop in a State identified in the report under paragraph (1).
“(B) Requirements—The workshop under subparagraph (A) shall identify regional strategies to support collaboration across the care continuum to promote antibiotic stewardship. In implementing such workshop, the Director of the Centers for Disease Control and Prevention should seek participation from relevant public and private stakeholders with expertise in infection control, quality improvement, and consumer engagement.
“(3) Authorization of appropriations—There is authorized to be appropriated, such sums as may be necessary to carry out this subsection.”
7. Other improvements
“(d) Continuing education on infection control and patient safety
“(1) In general—The Secretary shall establish a program to provide incentives (in the form of grants or other assistance) to State medical boards that require health care professionals (as defined by the medical board) to complete accredited coursework or training in infection control, antibiotic stewardship, or other patient safety topics as a condition of receiving a renewed license to practice in the State.
“(2) Exemption—A State medical board that receives assistance under paragraph (1) may provide an exemption from the coursework or training requirement under such paragraph for those health care professionals who have specialized training in infection control (such as an infectious disease specialist or certified infection control practitioner), who are not actively practicing in the State, or who do not provide direct patient care.
“(3) Authorization of appropriations—There is authorized to be appropriated, such sums as may be necessary to carry out this subsection.”
“(AA) in the case of hospitals, including critical access hospitals, to require that new members of the board of such hospital, not later than 6 months after joining the board, receive training (in accordance with criteria established by the Secretary) on patient safety topics that are relevant to a hospital (or critical access hospital, as the case may be) setting, such as infection prevention, care transitions, patient safety and quality of care measurement, and staff communication.”
“(d) Authority for direct reporting by patients
“(1) In general—A patient safety organization may collect information reported directly by patients on patient safety incidents and unsafe conditions. Such information shall not be deemed to be “identifiable patient safety work product”.
“(2) Requirements—In collecting patient safety information (including information submitted by patients under this subsection), a patient safety organization shall—
“(A) ensure that all such information (including any other patient safety work product received by the organization) is submitted to the network of patient safety databases; and
“(B) ensure that such information is de-identified prior to submitting the information to the network of patient safety databases.
“(3) Development of best practices—The Director of the Agency shall conduct research on best practices for enabling patient safety organizations to engage patients in reporting on patient safety incidents and for the collection by such organizations of such patient-reported information, including a standardized format for the submission of such data by patients. The Director shall disseminate such best practices for use by patient safety organizations.
“(4) Accessibility—The Director of the Agency shall establish a single access point on the Internet website of the Agency that may be accessed by the public to obtain patient safety data from the data that has been aggregated by the network of patient safety databases.
“(5) Authorization of appropriations—There is authorized to be appropriated, such sums as may be necessary to carry out this subsection.”