FEATURE ARTICLES

​​Taking care of ourselves is an important part of life. But more than that, we should be able to prevent, manage and understand any health problems that arise. This is called health literacy.

Health literacy is important because it helps people find the right health care and services, take care of a chronic condition or disease, or simply maintain their health and wellness.

The National Academies of Sciences, Engineering, and Medicine define health literacy as “the degree to which individuals have the capacity to obtain, process, and understand basic health information and services needed to make appropriate health decisions.

​​ACCORDING TO OFFICIAL WEB SITE OF THE U.S. HEALTH RESOURCES​ "Health Literacy"

Health literacy is the degree to which individuals have the capacity to obtain, process, and understand basic health information needed to make appropriate health decisions.
Low health literacy is more prevalent among:

Older adults
Minority populations
Those who have low socioeconomic status
Medically underserved people

What is our role in promoting health literacy?

Health literacy is a common thread through all of our programs. A large portion of the people we serve are poor and medically underserved.

They need help understanding and navigating a complex health care system. They require culturally competent providers who speak their language so they can make informed health care choices.

A number of patients may be confused with certain medical language, have difficulty understanding English, struggle with filling out forms, or have limited access to health providers in their community.

With the proper training, health care professionals can identify patients' specific health literacy levels and make simple communication adjustments."

A systematic review of the past 20 years literature showed "Low literacy has been linked to poor health outcomes such as higher rates of hospitalization and less frequent use of preventive services (see Fact Sheet: Health Literacy and Health Outcomes). Both of these outcomes are associated with higher healthcare costs." 

In 2015 the U.S. spent nearly $9,000 for the health of every American — far more than what the governments of other countries spend on the health of their citizens – yet life expectancy and health outcomes are generally worse for Americans than for citizens of other developed nations in North America and Europe.

​​The primary responsibility for improving health literacy lies with public health professionals and the healthcare and public health systems. We must work together to ensure that health information and services can be understood and used by all Americans. We must engage in skill-building with healthcare consumers and health professionals. Adult educators can be productive partners in reaching adults with limited literacy skills.

​​​Due to the increased complexity of the healthcare system, it is not surprising that this is creating more people with limited health literacy. ​As our healthcare system gets more complex and as a larger share of responsibility for self-management is moving into patients' hands, the ability to understand and process complex information is becoming increasingly important for getting good health outcomes. 

For the reasons of the high cost to treat disease in America, "disease prevention should be woven into all aspects of our lives, including where and how we live, learn, work and play. Everyone—government, businesses, educators, health care institutions, communities and every single American—has a role in creating a healthier nation.”​

HRSA A-ZIs something missing? If you want to see it in the A-Z index
A
About HRSA
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Black Lung Clinics Program
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CAREWare (Ryan White)
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data.hrsa.gov (formerly Data Warehouse)
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National Health Service Corps
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Office of Pharmacy Affairs – 340B Drug Pricing Program
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Poison Help Hotline 1-800-222-1222
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Radiation Exposure Screening & Education Program
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Teaching Health Centers
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Vaccine Injury Compensation
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Women's Health
Women's Preventive Services Guidelines
Date Last Reviewed:  August 2019

About HRSA

Tens of millions of Americans receive quality, affordable health care and other services through HRSA's 90-plus programs and more than 3,000 grantees.

HRSA programs provide equitable health care to people who are geographically isolated and economically or medically vulnerable. This includes programs that deliver health services to people with HIV, pregnant people, mothers and their families, those with low incomes, residents of rural areas, American Indians and Alaska Natives, and those otherwise unable to access high-quality health care. HRSA programs also support health infrastructure, including through training of health professionals and distributing them to areas where they are needed most, providing financial support to health care providers, and advancing telehealth. In addition, HRSA oversees programs for providing discounts on prescription drugs to safety net providers, facilitating organ, bone marrow, and cord blood transplantation, compensating individuals injured by vaccination, and maintaining data on health care malpractice payments.

Vision
Healthy Communities, Healthy People

Mission
To improve health outcomes and achieve health equity through access to quality services, a skilled health workforce, and innovative, high-value programs.

Goals

​Goal 1: Take actionable steps to achieve health equity and improve public health
Goal 2: Improve access to quality health services
Goal 3: Foster a health workforce and health infrastructure able to address current and emerging needs
Goal 4: Optimize HRSA operations and strengthen program engagement

Past Reports


Date Last Reviewed:  November 2021

About the National Vaccine Injury Compensation Program

The National Childhood Vaccine Injury Act of 1986 (PDF - 312 KB), as amended, created the National Vaccine Injury Compensation Program (VICP), a no-fault alternative to the traditional tort system. It provides compensation to people found to be injured by certain vaccines. Even in cases in which such a finding is not made, petitioners may receive compensation through a settlement.

The VICP was established after lawsuits against vaccine manufacturers and healthcare providers threatened to cause vaccine shortages and reduce vaccination rates. The Program began accepting petitions (also called claims) in 1988. 

What are VICP's objectives?

  • ensure an adequate supply of vaccines;
  • stabilize vaccine costs; and
  • establish and maintain an accessible and efficient forum for individuals found to be injured by certain vaccines. 


The 21st Century Cures Act (Public Law 114-255) (PDF – 729 KB), enacted on December 13, 2016, made several amendments to the National Childhood Vaccine Injury Act of 1986. 
What were the amendments?

  • Expand the VICP’s coverage to include new categories of vaccines that previously were not covered by the VICP: vaccines recommended by the CDC for routine administration to pregnant women (but not for routine administration in children) and subject to a federal excise tax. See Section 3093(c)(1) of P.L. 114-255.
  • Make clear that vaccine-injury claims may be filed both with respect to injuries alleged to have been sustained by women receiving covered vaccines during pregnancy and with respect to injuries alleged to have been sustained by live-born children who were in utero at the time those women were administered such vaccines. See Section 3093(c)(2), (3) of P.L. 114-255.


Who administers VICP?

The Division of Injury Compensation Programs, Healthcare Systems Bureau, Health Resources and Services Administration, U.S. Department of Health and Human Services administers VICP.

Which federal organizations have a role in the VICP?

  • U.S. Department of Health and Human Services (HHS) hosts the Program, conducts medical reviews of petitions, and makes Court-ordered compensation payments;
  • U.S. Department of Justice (DOJ) represents HHS in Court; and
  • U.S. Court of Federal Claims (the Court) makes the final decision regarding whether a petition is compensated and the type and amount of compensation.


What is the Vaccine Injury Compensation Trust Fund?
The Vaccine Injury Compensation Trust Fund provides funding for the National Vaccine Injury Compensation Program to compensate vaccine-related injury or death petitions for covered vaccines administered on or after October 1, 1988.
Funded by a $.75 excise tax on vaccines recommended by the Centers for Disease Control and Prevention for routine administration to children, the excise tax is imposed on each dose (i.e., disease that is prevented) of a vaccine. Trivalent influenza vaccine for example, is taxed $.75 because it prevents one disease; measles-mumps-rubella vaccine, which prevents three diseases, is taxed $2.25.

The Department of Treasury collects the excise taxes and manages the Fund’s investments and produces Vaccine Injury Compensation Trust Fund Monthly Reports.

Advisory Commission on Childhood Vaccines
The Advisory Commission on Childhood Vaccines, consisting of nine voting members, advises and makes recommendations to the Secretary of Health and Human Services, on issues relating to the operation of the VICP and on ways to improve it.

Frequently Asked Questions
For more information, read the FAQs.

​DisclaimerThe content of this website reflects the current thinking of the United States Department of Health and Human Services on the topics addressed and does not create or confer any rights for or on any person and does not operate to bind the Department or the public. The ultimate decision about the scope of the statutes authorizing the VICP is within the authority of the United States Court of Federal Claims, which is responsible for resolving petitions for compensation under the VICP.
If you have additional questions, call: 1-800-338-2382 or email: vaccinecompensation@hrsa.gov.

Date Last Reviewed:  March 2022

​​Who Can File a PetitionYou may file a petition if you:

  • received a covered vaccine and believe that you have been injured by the vaccine,
  • are the parent or legal guardian of a child or disabled adult who received a covered vaccine and whom you believe was injured by the vaccine, or
  • are the legal representative of the estate of a deceased person who received a covered vaccine and who you believe was injured by the vaccine and/or whose death you believe resulted from that vaccination.


You may file a petition regardless of your age and whether or not you are a U.S. citizen. The covered vaccine must have been given in the United States or its trust territories unless:

  • the person who received the vaccine was, at the time of vaccination, a U.S. citizen serving abroad as a member of the Armed Forces or as an employee of the U.S. Government, or a dependent of such a citizen; or
  • the vaccine’s manufacturer was located in the United States and the person who received the vaccine returned to the United States within six months after the date of vaccination.


Severity Requirements

You can file a petition when the effects of the injury:

  • lasted for more than six months after the vaccination; or
  • resulted in inpatient hospitalization and surgical intervention; or
  • resulted in death.


Filing Deadlines

You must file your petition within the following timeframes:

  • Injury: within three years after the first symptom or manifestation of onset or of the significant aggravation of the injury;
  • Death: within two years of the death and within four years of the first symptom or manifestation of onset or of the significant aggravation of the injury from which the death resulted;
  • Certain Vaccine Injury Table (Table) changes: two years from the date of the Table change for injuries or deaths that occurred up to eight years before the Table change. A Table change includes new vaccines or injuries added to the Table or other changes to the Table if the revision makes a petitioner eligible to seek compensation or significantly increases the likelihood of a petitioner obtaining compensation. 
  • The Court may extend a deadline using equitable tolling in very limited circumstances.


Frequently Asked QuestionsFor more information, read the FAQs.

DisclaimerThe content of this website reflects the current thinking of the United States Department of Health and Human Services on the topics addressed and does not create or confer any rights for or on any person and does not operate to bind the Department or the public. The ultimate decision about the scope of the statutes authorizing the VICP is within the authority of the United States Court of Federal Claims, which is responsible for resolving petitions for compensation under the VICP.

If you have additional questions, call: 1-800-338-2382 or email: vaccinecompensation@hrsa.gov.

​​How to File a Petition
COVID-19 Claims

For claims associated with the COVID-19 vaccine or other COVID-19 related countermeasures, please file your Request for Benefits with the Countermeasures Injury Compensation Program.

To be compensated by the National Vaccine Injury Compensation Program (VICP), you must file a petition with the U.S. Court of Federal Claims and a copy of the petition must sent to the Department of Health and Human Services.

The petition is a legal document that you can prepare yourself, or hire a lawyer to prepare and file on your behalf. Because this is a legal process, most people hire a lawyer.

The Court generally will award reasonable attorneys' fees and other legal costs as long as your petition is deemed reasonable and filed in good faith.

Visit the U.S. Court of Federal Claims, Office of Special Masters for detailed information about how to submit a petition, including guidelines, sample filings and a list of attorneys who have agreed, upon request, to accept referrals in certain vaccine injury cases.

Where do I file my petition?

Submit your petition, one original and two copies, including cover sheet, medical records, and other documentation plus the appropriate filing fee to:

Clerk
U.S. Court of Federal Claims
717 Madison Place NW
Washington, DC 20439

If you are unable to pay the filing fee, call 202-357-6400.

Where must I send a copy of the petition?

After you submit your petition to the U.S. Court of Federal Claims, you must either submit an electronic copy on the HRSA Injury Compensation Programs website or mail in a copy of the petition.

How do I submit a copy of the petition electronically?On the HRSA Injury Compensation Programs website, follow the step-by-step instructions on the How to Create an Account page, and then log in with your username and password. After login, select the Submit button under Submit a Petition to VICP on the home page. Fill out the required fields to submit a copy of the petition.

For more information about VICP, contact 1-800-338-2382 or vaccinecompensation@hrsa.gov.
Or…

How do I submit a copy of the petition by mail?After you submit your petition to the U.S. Court of Federal Claims, submit a copy of the petition by mail to the following address:

Secretary, Health and Human Services
Health Resources and Services Administration
Director, Division of Injury Compensation Programs
National Vaccine Injury Compensation Program (VICP)
5600 Fishers Lane, 08N146B
Rockville, MD 20857

DisclaimerThe content of this website reflects the current thinking of the United States Department of Health and Human Services on the topics addressed and does not create or confer any rights for or on any person and does not operate to bind the Department or the public. The ultimate decision about the scope of the statutes authorizing the VICP is within the authority of the United States Court of Federal Claims, which is responsible for resolving petitions for compensation under the VICP.
If you have additional questions, call: 1-800-338-2382 or email: vaccinecompensation@hrsa.gov.

Vaccine Injury Compensation Data
Most Recent Data Report

National Vaccine Injury Compensation Program Data Report (PDF - 249 KB) - updated March 1, 2022.

Updated monthly, and includes the number of

  • petitions filed;
  • adjudications compensated and dismissed;
  • awards paid by type and amount;
  • claims by vaccine; and
  • adjudication categories by vaccine.


The United States has the safest, most effective vaccine supply in history. In the majority of cases, vaccines cause no side effects, however they can occur, as with any medication—but most are mild. Very rarely, people experience more serious side effects, like allergic reactions.

In those instances, the National Vaccine Injury Compensation Program (VICP) allows individuals to file a petition for compensation.

What does it mean to be awarded compensation?

Being awarded compensation for a petition does not necessarily mean that the vaccine caused the alleged injury. In fact:

  • Approximately 60% of all compensation awarded by the VICP comes as result of a negotiated settlement between the parties in which HHS has not concluded, based upon review of the evidence, that the alleged vaccine(s) caused the alleged injury.
  • Attorneys are eligible for reasonable attorneys’ fees, whether or not the petitioner is awarded compensation by the Court, if certain minimal requirements are met. In those circumstances, attorneys are paid by the VICP directly. By statute, attorneys may not charge any other fee, including a contingency fee, for his or her services in representing a petitioner in the VICP.


What reasons might a petition result in a negotiated settlement?

  • Consideration of prior U.S. Court of Federal Claims decisions, both parties decide to minimize risk of loss through settlement
  • A desire to minimize the time and expense of litigating a case  
  • The desire to resolve a petition quickly


​DisclaimerThe content of this website reflects the current thinking of the United States Department of Health and Human Services on the topics addressed and does not create or confer any rights for or on any person and does not operate to bind the Department or the public. The ultimate decision about the scope of the statutes authorizing the VICP is within the authority of the United States Court of Federal Claims, which is responsible for resolving petitions for compensation under the VICP.

If you have additional questions, call: 1-800-338-2382 or email: vaccinecompensation@hrsa.gov.

Black Lung Clinics Program

We fund the Black Lung Clinics Program (BLCP). This program treats coal miners with job-related coal mine dust lung disease.


Who does BLCP help?

The program serves active, inactive, retired, and disabled US coal miners.

Does BLCP serve patients directly?

We fund Black Lung Clinics. These clinics may serve patients directly or through health care providers such as:

  • Federally Qualified Health Centers
  • Hospitals
  • State health departments
  • Mobile vans
  • Clinics


What services does BLCP support?

  • Outreach and education to raise awareness of Black Lung diseases
  • Primary care (including screening, diagnosis, and treatment)
  • Patient and family education (including anti-smoking education)
  • Benefits counseling (including state and federal compensation programs)
  • Patient care and coordination (including individual patient care plans and referrals as needed)
  • Pulmonary rehabilitation to improve breathing​​



Can my facility participate?

Any state or public or private entity may apply. All applicants, at a minimum, must provide certain services to coal miners in their service area. Federally recognized tribes or tribal organizations that want to apply are eligible if they conduct all proposed activities within federally recognized tribal areas.

Who are the awardees?

We awarded approximately $11.2 million in Fiscal Year (FY) 2020 to the following grantees:


Grantee Organization                                                                           City                            State

Canyonlands Healthcare                                                                                Page                              AZ
National Jewish Health                                                                                   Denver                          CO
University of Illinois - Chicago                                                                      Chicago                       IL
Big Sandy Health Care                                                                                     Prestonsburg             KY
Owensboro Health Muhlenberg Community Hospital                             Greenville                   KY
Miners’ Colfax Medical Center                                                                       Raton                           NM
Genesis Healthcare System                                                                            Zanesville                  OH
UPMC Altoona                                                                                                     Altoona                       PA
Lungs at Work                                                                                                     Canonsburg              PA
Centerville Clinic                                                                                                Fredericktown          PA
Community Health of East Tennessee                                                          Lafollette                   TN
Stone Mountain Health Services                                                                   Jonesville                   VA
West Virginia Department of Health and Human Resources                  Charleston               WV
Reynolds Memorial Hospital                                                                           Glen Dale                  WV
Northwest Community Action Programs of Wyoming                              Worland                    WY

Related Resources

Black Lung Data and Resource Center  (BLDRC)
BLDRC improves patient-level data collection and analysis, clinic operations, and the quality and breadth of services that BLCP recipients provide.

Black Lung Program – 340B Program Savings
Black Lung Clinics can participate in the 340B Drug Pricing Program to save money on prescription drugs and use those savings to improve and expand patient care.

Black Lung Clinics Program 2017-2020 Cohort Snapshot (PDF - 1.63 MB)
This provides information on each of the 15 awardees across the 2017 – 2020 cohort, including demographics, promising practices, challenges, and major accomplishments.

Federal Programs

Department of Labor
Division of Coal Mine Workers’ Compensation Program
Mine Safety and Health Administration

Centers for Disease Control and Prevention
Coal Workers’ Health Surveillance Program

Celebrating 40 Years

In 2019 BLCP celebrated 40 years of supporting coal miners throughout the country. View the history, progress, and impact of BLCP on miners' lives.

​Contact UsJason Rush
Email: blacklung@hrsa.gov
Phone: 301-945-3054

Date Last Reviewed:  November 2021

Lower Extremity Amputation Prevention (LEAP)

Lower Extremity Amputation Prevention (LEAP) can dramatically reduce lower extremity amputations in individuals with Hansen's disease or any condition that results in loss of protective sensation in the feet.

HRSA's National Hansen's Disease Program (NHDP) developed LEAP in 1992.

The Five-Step LEAP Program

STEP ONE: Annual Foot Screening

The foundation of this prevention program is a foot screening that identifies those patients who have lost protective sensation.

The initial plantar ulcer usually results from an injury to a foot that has lost sensation. In the absence of protective sensation, even normal walking can result in such injuries.

The LEAP Foot Screen uses a 5.07 monofilament, which delivers 10 grams of force, to identify patients with a foot at risk of developing problems.

Perform an initial foot screen on all patients at diagnosis and at least annually thereafter.
To help prevent foot problems, at-risk patients should be seen at least four times a year. This is to check their feet and shoes to help prevent foot problems from occurring.

STEP TWO: Patient Education

Teaching the patient self-management skills is the second component of the LEAP Program.
Once taught simple self-management techniques, the patient assumes personal responsibility and becomes a full partner with the health care team in preventing foot problems.

STEP THREE: Daily Self-Inspection

Daily self-inspection is an integral part of the self-management program.

Every individual who has lost protective sensation must regularly and properly examine their feet on a daily basis.
Studies have shown that daily self-inspection is the single most effective way to protect feet in the absence of the pain warning system.

Early detection of foot injuries (blister, redness, or swelling), callus or toe nail problems (thick, tender, long, or discolored) is necessary to prevent potentially more serious problems.

Some problems should be reported immediately to a health care provider while the patient can manage others if they have been taught simple, basic self-management techniques.

STEP FOUR: Footwear Selection

Shoes, like feet, come in a variety of styles and shapes.

A person with normal sensation in their feet can wear almost any shoe style with little risk of injury. If the patient has lost protective sensation, poorly designed or improperly fitting shoes can seriously complicate the condition of the feet.

Once a patient has lost protective sensation, they should never walk barefoot, even around the house.
The patient should never wear narrow toe shoes or boots, heeled shoes, shoes with vinyl tops, thongs or any shoe that is too loose or too tight.

This person will need special assistance in selecting the appropriate style and fit of shoes.

The shoe should fit the shape of the foot. There should be at least ½ inch between the longest toe and the end of the shoe.

In a properly fitting shoe, a small amount of leather can be pinched up.

The patient, the family and the health care team need to recognize that wearing appropriately styled shoes that fit can prevent most foot problems.

STEP FIVE: Management of Simple Foot Problems

In addition to causing loss of protective sensation, neuropathy can also affect the autonomic nerves in the foot. And this can lead to dry cracked skin, increasing the probability of foot injuries and wounds.

This prevention program emphasizes the importance of reporting all injuries to the health care provider.

Date Last Reviewed:  June 2019

​Opioid Crisis
The Nation is in the midst of an unprecedented opioid epidemic. More than 130 people a day die from opioid-related drug overdoses

Prevention and access to treatment for opioid addiction and overdose reversal drugs are critical to fighting this epidemic. Primary care settings have increasingly become a gateway to better care for individuals with both behavioral health (including substance use) and primary care needs.

The Health Resources and Services Administration (HRSA) supports its grantees with resources, technical assistance, and training to integrate behavioral health care services into practice settings and communities. 

How HRSA is Addressing the Opioid Crisis

Expanding access through health centers and other primary care settings
Using telehealth to treat opioid use disorder
Connecting stakeholders to opioid-related resources
Sharing best practices and regional approaches
Increasing opioid use disorder training in primary care
Informing policy and future investments
Addressing opioid-related poisonings and overdoses

Oral Health

Oral health is an integral part of overall health. To increase access to quality oral health care, HRSA provides support for oral health programs, activities, and initiatives.

To increase early detection and prevention, and improve overall health, HRSA developed the Integrating Oral Health and Primary Care Practice (IOHPCP) (PDF – 784 KB) initiative. This initiative seeks to improve the knowledge and skills of primary care clinicians and promote interprofessional collaboration across health professions.

Additionally, in response to recommendations from the National Academy of Medicine (NAM) , HRSA identified five key oral health domains and associated core clinical competencies.

Risk Assessment
Oral Health Evaluation
Preventive Intervention
Communication and Education
Interprofessional Collaborative Practice

How Do These Work in Practice?

In 2013, HRSA awarded the National Network for Oral Health Access (NNOHA) funding to pilot the oral health competencies in three health centers across the country.

User's Guide for Implementation of Interprofessional Oral Health Core Clinical Competencies: Results of a Pilot Project (PDF – 4.7 KB) describes the challenges associated with developing a new program, strategies to address these challenges, and recommendations for implementing the program in primary care settings.
Webinars


Which Programs Address Oral Health?

HRSA bureaus and offices support a variety of programs, activities, and initiatives that improve oral health.
Office of Planning, Analysis, and Evaluation (OPAE)OPAE provides HRSA-wide oral health leadership for cross-agency initiatives and departmental priorities. They also administer the National Organizations for State and Local Officials (NOSLO) and National Forum for State and Territorial Chief Executives (National Forum) cooperative agreement programs which supports activities that address oral health.

Agency-wide efforts


NOSLO


Maternal and Child Health Bureau (MCHB)


Ryan White HIV/AIDS Bureau (HAB)

The Ryan White HIV/AIDS Program provides related care and services to more than 500,000 people every year, including dental programs to address the unique health issues faced by people living with HIV/AIDS.

Bureau Health Workforce (BHW)Oral Health Workforce Development Programs help build and train the oral health workforce, improving access to quality oral healthcare for those most in need.

The National Health Service Corps offers loan repayments and scholarships for health care professionals, including dentists and dental hygienists that practice in Health Professional Shortage Areas (HPSAs).

The National Center for Health Workforce Analysis supports Health Workforce Research Centers at various universities through cooperative agreements including the Oral Health Workforce Research Center at the State University of New York at Albany.

Bureau of Primary Health Care (BPHC)

HRSA's Health Center program increases access to quality primary health care services, including oral health, for medically underserved populations. Most grantees also provide dental services either on-site or by paid referral.

  • 2016: 420 health center grantees received additional funding to increase oral health services as part of the HRSA Oral Health Expansion Supplement effort. 
  • 2016: Health centers provided more than 14 million dental visits — an increase of 56% since 2010.


Office of Rural Health Policy (ORHP)

  • Rural Health Care Services Outreach program supports projects that demonstrate creative and effective models of outreach and service delivery in rural communities.
    • In 2017, ORHP awarded 60 new Outreach Grants, including 11 new grantees with a focus in oral health care delivery. These programs seek to improve access to affordable oral health care services in rural areas.
  • Rural Oral Health Toolkit  helps programs to identify and implement oral health services and provides examples of resources and best practices.
  • Rural Health Network Development supports rural integrated health care network, integrating systems of care administratively, clinically and financially.
    • Two grantees are engaged in oral health projects.


Date Last Reviewed:  February 2018

About the Office of Women's Health

Mission

To advance health and wellness for women across the lifespan by leading and promoting innovative, sex and gender-responsive public health approaches

Vision

Healthy women, healthy communities

Core Functions

OWH provides leadership on women's health and sex/gender-specific issues.
We work within and outside of the U.S. Department of Health and Human Services to improve the health, wellness, and safety of women across the lifespan.

We accomplish this through the following core functions:

  • Provide subject matter and technical expertise to HRSA’s Administrator on health issues impacting women across the lifespan
  • Lead cross-agency collaborations with HRSA bureaus and offices and other federal and non-federal partners to address key issues of concern for women
  • Consult with organizations and key stakeholder groups to inform HRSA investments in women’s health


Date Last Reviewed:  
May 2021

Women’s Preventive Services Guidelines

Affordable Care Act Expands Prevention Coverage for Women’s Health and Well-Being

The Affordable Care Act (ACA) – the health insurance reform legislation passed by Congress and signed into law by President Obama on March 23, 2010 – helps make prevention services affordable and accessible for all Americans by requiring most health insurance plans to provide coverage without cost sharing for certain recommended preventive services. Preventive services that have strong scientific evidence of their health benefits must be covered and plans can no longer charge a patient a copayment, coinsurance or deductible for these services when they are delivered by a network provider.

Under the ACA, most private health insurers must provide coverage of women’s preventive health care – such as mammograms, screenings for cervical cancer, prenatal care, and other services –with no cost sharing. Under section 2713 of the Public Health Service Act, as modified by the ACA, non-grandfathered group health plans and non-grandfathered group and individual health insurance coverage are required to cover specified preventive services without a copayment, coinsurance, deductible, or other cost sharing, including preventive care and screenings for women as provided for in comprehensive guidelines supported by HRSA for this purpose.

The law recognizes and HHS understands the unique health needs of women across their lifespan. The purpose of WPSI is to improve women’s health across the lifespan by identifying preventive services and screenings to be used in clinical practice and, when supported by HRSA, incorporated in the Guidelines.

HRSA-Supported Women’s Preventive Services Guidelines: Background

The HRSA-supported Women’s Preventive Services Guidelines (Guidelines) were originally established in 2011 based on recommendations from a Department of Health and Human Services' commissioned study by the Institute of Medicine  (IOM), now known as the National Academy of Medicine (NAM).

Since the establishment of the Guidelines, there have been advancements in science and gaps identified in clinical practice. To address these, in 2016, the Health Resources and Services Administration (HRSA) awarded a five-year cooperative agreement, the Women’s Preventive Services Initiative (WPSI), to the American College of Obstetricians and Gynecologists (ACOG) to convene a coalition of clinician, academic, and consumer-focused health professional organizations to conduct a scientifically rigorous review to develop recommendations for updated Guidelines in accordance with the model created by the NAM Clinical Practice Guidelines We Can Trust. The American College of Obstetricians and Gynecologists (ACOG) formed an expert panel, also called the WPSI, for this purpose.

In March 2021, ACOG was awarded a subsequent cooperative agreement to review and recommend updates to the Guidelines. Under ACOG, WPSI reviews existing Women’s Preventive Services Guidelines biennially, or upon the availability of new evidence, as well as new preventive services topics. New topics for future consideration can be submitted on a rolling basis at the Women’s Preventive Services Initiative website .

HRSA-Supported Women's Preventive Services Guidelines

HRSA supports the Guidelines listed below that address health needs specific to women. In December 2021, HRSA approved a new guideline on obesity prevention for midlife women and updates to five existing preventive services guidelines: Well-Women Preventive Visits, Breastfeeding Services and Supplies, Counseling for Sexually Transmitted Infections (STIs), Screening for Human Immunodeficiency Virus (HIV) Infection, and Contraception.*