This site is intended for Healthcare professionals only.

ACOG Guidelines for performing office-based procedures including Abortion


ACOG Guidelines for performing office-based procedures including Abortion

Washington, D.C. — American College of Obstetricians and Gynecologists (ACOG) along with the National Partnership for Women & Families released the results of “The Project on Facility Guidelines for the Safe Performance of Primary Care and Gynecology Procedures in Offices and Clinics”. The goal of the Project was to further healthcare quality, safety, affordability, and patient experience without imposing unjustified burdens on patients’ access to care or on clinicians’ ability to provide care within their scope of practice. The findings were published in Obstetrics & Gynecology.

“This collaborative effort among women’s groups and women’s health experts found that guidelines for facilities performing office-based procedures, including abortion, are already comprehensive and adequate,” said Barbara S. Levy, MD, ACOG Vice President of Health Policy. “Regulations or laws requiring changes to currently accepted practices for such procedures are unwarranted and add burden to women and providers without improving safety. Our organizations must now focus on reducing the burden to improve clinicians’ ability to provide care and women’s ability to access that care.”

To date, the organizations listed below have endorsed the guidelines:

  • American Academy of Family Physicians (AAFP)
  • American Academy of Nursing (AAN)
  • American Academy of Physician Assistants (AAPA)
  • American College of Nurse-Midwives (ACNM)
  • American College of Obstetricians and Gynecologists (ACOG)
  • American College of Osteopathic Obstetricians and Gynecologists (ACOOG)
  • American College of Physicians (ACP)
  • American Public Health Association (APHA)
  • National Hispanic Medical Association (NHMA)
  • National Partnership for Women & Families (NPWF)
  • Nurse Practitioners in Women’s Health (NPWH)
  • Planned Parenthood Federation of America (PPFA)
  • Society of Family Planning (SFP)
  • Society of General Internal Medicine (SGIM)

The Key features of  Guidelines are-

Emergency Preparedness 

  • Facilities should establish written policies and procedures for managing facility emergencies (e.g., natural disaster, fire) and patient emergencies (e.g., vasovagal reaction, hemorrhage) and should conduct periodic drills and staff trainings on those policies and procedures. A formal transfer agreement with a hospital is not required as transfers are rare and hospitals are required to accept patients with emergent needs. Good communications in the event of a transfer and working relationships with facilities that may receive or refer patients are encouraged.
  • Facilities should have a staff person trained in basic life support onsite when procedures are performed and have a person other than the clinician performing the procedure onsite to provide assistance, call for additional assistance, or transport to a hospital in an emergency.
  • Facilities should maintain adequate supplies for basic life support and medications and equipment needed to treat emergencies that may occur with the procedures performed.
  • Facilities should provide basic emergency lighting (e.g., battery backup lighting, flashlights).
  • Facilities should keep doorways and hallways free of obstructions that could impede exit by patients and staff or ingress by emergency personnel. Where the types and risks of procedures performed at the facility create a reasonable likelihood that patient transfer by stretcher may be needed, doorways and hallways in the path of egress should be sufficiently wide to permit passage by stretcher (note that this term includes chair stretchers, which can be maneuvered through typical office doorways and hallways).
  • Facilities should provide wayfinding signage that is understandable to the patient population served.

Biological Material Handling 

  • Facilities should establish written policies and procedures for properly labeling, handling, and storing biological specimens to be sent to pathology or other laboratory. The decision of whether to send specimens for pathology evaluation is made by the clinician or on the basis of facility policies.
  • Facilities should establish written policies and procedures for handling, storing, and disposing of hazardous materials in a manner that minimizes the risk of exposure and for reducing the risk of harm to individuals involved, should exposure occur. Tissue not sent to pathology should be disposed of in the same manner as other biological materials. Tissue used in research or commercial endeavors is subject to separate requirements not addressed in this document.
  • Facilities should conduct periodic staff training on the policies and procedures described.

Physical Plant Specifications 

  • Facilities should consider patient privacy, confidentiality, and comfort in the design and flow of the facility.
  • Facilities should perform procedures in exam rooms or procedure rooms adequate to accommodate the equipment and personnel involved in the procedure. Typical exam rooms are an adequate size for most procedures; a room larger than needed to accommodate the equipment and personnel involved in the procedure is neither necessary nor desirable.
  • Facilities should have patients recover in the room in which the procedure was performed or in a separate recovery room or area. A separate recovery room is not required. Some procedures require no recovery time.
  • Facilities should provide separate storage for clean and dirty supplies.
  • If instruments are sterilized onsite, facilities should provide separate marked areas for soiled and clean instrument processing. Separate rooms for those functions are not required. Offsite sterilization services may also be used.
  • Facilities should provide a source of emergency power for equipment if any of the procedures performed in the facility are ones where a power loss during the procedure would threaten patient safety.
  • Facilities should have onsite, and maintain in good condition, the equipment needed for the procedures performed.
  • Facilities should utilize adequate heating, ventilation, and cooling systems. Systems typical for offices are adequate in this context; no special heating, ventilation, or cooling systems are needed.
  • Facilities that store specimens or medications requiring refrigeration should provide separate refrigerated storage for each.

Facility Accreditation and Licensing 

  • Procedures should be provided in facilities that meet current accepted practices. Such accepted practices do not require facility accreditation or facility licensing.

Clinician Qualifications Beyond Licensing 

  • Facilities should ensure that clinical staff are trained in the procedures performed, equipment used in the facility, basic life support, cultural sensitivity, and any requirements governing the facility with regard to accommodations to facilitate safe and appropriate access to health services for individuals with disabilities or other conditions, including limited English proficiency. While some facilities will have no need for nursing staff, facilities should ensure that any clinical duties requiring nursing care are staffed appropriately.
  • Facilities should designate a clinician responsible for ensuring that clinicians who perform procedures at the facility have established competence in those procedures. Such competence may be established through any of a variety of training, education, and assessment activities (which may be specified by the facility, a professional organization, or specialty). Neither board certification nor hospital privileges is required.

Other Policies and Procedures 

  • Facilities should establish written policies and procedures for infection control, conduct periodic staff training on those policies and procedures, and implement a plan to monitor compliance.
  • Facilities that perform procedures on more than an occasional basis should establish a written quality improvement plan that includes recording and reviewing available facility data on select adverse outcomes related to procedures performed and ways to act on information gained.
  • Facilities should establish a written policy and schedule for checking equipment functioning.
  • Facilities should establish a written policy and schedule for managing medication inventory.

For more details click on the link: www.acog.org



Source: self

Share your Opinion Disclaimer

Sort by: Newest | Oldest | Most Voted
  1. user
    Dr Geraldine Sanjay January 31, 2019, 6:51 pm

    How can killing babies in the Womb be considered an office procedure❓The baby is disposed off as biological material.Will God forgive us for this grave crime against his innocent. Creations❓