US Healthcare Policies and Delivery Systems
How did we get here?
An Overview of US healthcare History
Healthcare in the US has grown with new discoveries, innovations and technologies. This page is an overview of important milestones within the history of US Healthcare.
Colonial through the early 1900s
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Medical care in the United States was primitive in nature from 1776 until the early 1900s. Those involved in care were limited to patients, their families and the physician. “Physicians set and often adjusted their charges to estimates of patients’ ability to pay and collect their own bills.” (Sultz and Young, 2018, P.24.) During this time doctor’s education was informal and those doctors were often difficult for patients to get to. While some doctors spent time as an apprentice beneath another doctor, there were no requirements for doctors in the colonial era. The first medical school was founded by John Morgan and William Shippen JR in 1765 at the College of Philadelphia. (Penn) Regulations began to come about in the mid-1700s and doctors began to have to become certified. According to MedlinePlus, U.S. National Library of Medicine, “Professional societies began regulating medical practice by examining and licensing practitioners as early as 1760. By the early 1800s, the medical societies oversaw establishing regulations, standards of practice, and certification of doctors.” An important association that formed in this time period was the AMA, or the American Medical Association. According to their website they were founded in 1847. With these changes came the introduction of what is considered the first form of insurance. This insurance was brought about in the 1800s. It isn’t the typical insurance you would see today and according to Sultz & Young (2018), “Sickness insurance, as it was originally called, was the beginning of social insurance programs that mitigated the risks of income interruption by accident, sickness, or disability. Initially such insurance was provided only to wage earners.”(P.24) This insurance was all that was seen until 1915. There was a need for insurance to be required by law. European countries had played a re role in influencing the US in their campaign for healthcare. They already had subsidies and required healthcare. Two things stalled this campaign, WWI and the AMA. (Sultz and Young, 2018, P.24)
The great Depression
The great depression was a rough time for many, and this didn’t exclude hospitals and physicians. 1929 was the start of many financial downfalls. People couldn’t afford to pay medical bills which caused admission rates to plummet. This lack of income for physicians and hospitals brought on experiments with health insurance. The birth of Blue cross was from one of these experiments brought to light by Baylor. According to Sultz and Young (2018), “The Baylor University Hospital plan was not the first, but it became the most influential of those insurance experiments. By enrolling 1,250 public school teachers at 50 cents a month for a guaranteed 21 days of hospital care, Baylor created the model for, and is credited with the genesis of, Blue Cross hospital insurance.”(P.24) These experiments grew into plans that were put to action. The American people needed something to help them with the costs. According to Sultz & Young (2018) this was delivered, “By 1937, there were 26 plans with more than 600,000 members, and the American Hospital Association began approving the plans.”(P.24) The AMA still didn’t support this push for healthcare. This is when government intervention started, which the AMA supported.
The ever-growing influence of government on healthcare
Healthcare costs continued to rise, and it wasn’t completely caused by insurance companies. The government’s influence and role in coverage of health care for special populations shares a portion of the blame. “In 1935, by granting federal aid to the states for public health and welfare assistance, maternal and child health, and children with disabilities services, the Social Security Act became the most significant social policy ever passed by any Congress.” (Sultz & Young,2018, P.25) This as well as the Health Professions Educational Assistance Act of 1963 and the Nurse Training Act helped to pave the way to what was to happen next. Medicaid and Medicare were signed into action by President Lyndon B. Johnson on July 30, 1965. These plans covered older adults and low-income families. This would change in later years to cover more of the population in need. The government supported and was involved in many programs through the years. The need for assistance grew as the cost of healthcare continued to rise. This caused insurance premiums to rise with lack of control over physician and hospitals costs. “Over the years, the U.S. government developed, revised, and otherwise adjusted a host of categorical or disease-specific programs designed to address needs not otherwise met by state or local administrations or the private sector. Today, federally sponsored programs account for about 43 percent of U.S. personal healthcare expenditures.” (Sultz & Young, 2018, P.26) The introduction of block grants began an era labeled as “New Federalism”. In 1970, President Nixon wanted to make a shift in the federal government’s direct influence within healthcare programs. He had a vision of using these block grants to let the states utilize at their discretion funds that were utilized for specific programs. This would give the states and local government more control and say to where the money went and how it was used.
While the government was trying to make healthcare more affordable, they were contributing to the constant growth in how much healthcare cost. The programs set in place brought healthcare to many who couldn’t afford it, while at the same time causing a tremendous expenditure. According toSultz and Young (2018), “In the mid-1960s, when Medicare and Medicaid were passed, the United States was spending about $42 billion on health care, or approximately 8.4 percent of the gross domestic product. The costs of U.S. health care now exceed $3 trillion and consume more than 17 percent of the gross domestic product.”(P.26) While costs had grown astronomically there was another notable attempt at controlling them during the Reagan Administration. Diagnosis-related groups or DRGs was brought forth during the 80s to encourage physicians and healthcare facilities to utilize their resources efficiently. The implementation of the Medicare prospective payment system in hospitals caused a shift from what Sultz and Young (2018) calls “a fee-for-service retrospective mode to a pre-paid prospective mode.”(P.28) Rather than charging for the service they were to charge per diagnoses. According to Sultz and Young (2018) the Reagan Administration also tried to control costs by, “the administration also created a new payment method, the resource-based relative value scale (RBRVS) to make physician payments equitable across various types of service, specialties, and geographic locations.”(P.28 ) This wasn’t the end of the government trying to regulate costs within the healthcare system. In 1997 with the introduction of the Balanced Budget Act, the government took steps in reducing costs and balancing the budget. While cost was being addressed there was now a concern for quality and access. With coverage being made for the low-income population, this was causing a cost shift for those with other insurance. This combined with hospitals and physicians doing their own thing and interpreting the regulations loosely has caused quality and access to become an issue.
Quality, Cost and Access control
Though there was a continuous effort with the government to make healthcare more affordable, there was little to no effort in the population having access and good healthcare quality. Legislation compliance was open for interpretation from hospital administrators and physicians. Interpretations were often left loose so that way they could get more for less. In 2010 when the affordable care act was in place this started to change. The Affordable Care Act, also known as “Obamacare”, has helped to change the face of healthcare through reimbursement. This requires healthcare facilities and providers to offer what Sultz and Young (2018) calls, “value-based, rather than volume-based reimbursement.”(P.36 ) Prior to the ACA there had been attempts to address this triangle of issues. Sultz and Young (2018) discusses two initiatives, the Public Health Service Act of 1965 and the Comprehensive Health Planning Act of 1966.(P.27) These two initiatives were both meant to address the three concerns. While intentions were in the right place the Public Health Service Act according to Sultz and Young (2018) allowed for “representatives of each constituency to put their focus on advocating for funding in their respective disciplines. Consequently, the regional medical programs added educational and clinical resources but did not materially improve prevention or cost reductions in the treatment of the target conditions.” (P.27 ) The second attempt at addressing the three concerns was passed in 1966. This was the Comprehensive Health Planning Act. Both programs were unable to attain the goals in mind when enacting them. This was highly due to allocation of research and development funds being a conflict of interest. (Sultz & Young, 2018, P27) In another attempt to fix the issues the National Health Planning and Resources Development Act of 1974 combined the Regional Medical Health Program and Comprehensive Health Planning Act programs. The birth of HSAs was the result of this combination. According to Sultz and Young (2018), “HSAs required representation of healthcare providers and consumers on governing boards and committees to deliberate and recommend healthcare resource allocations to federal and state authorities.”(P.27 ) This attempt was also counted as a failure which led to the support of the federal government to be withdrawn. In another attempt that was successful until the 1990s, the Health Maintenance Organization Act was enacted in 1973. An HMO is an organization responsible for the financing and delivery of comprehensive health services to an enrolled population for a prepaid, fixed fee.(Sultz & Young, 2018, P.28 ) Through this Act, healthcare started seeing a step towards preventative health. According to Sultz and Young (2018), rising costs and consumer complaints caused “a consumer and provider backlash resulted in all 50 states enacting protections against managed care access and cost restrictions.”(P.28 ) This led to PPOs or Preferred Provider Organizations in the 2001. While there were managed care characteristics from HMOs, physicians and hospitals organized PPOs. They had catered PPOs to meet consumer needs.
Technological Advancements and New Problems
The world has always been improving healthcare with advancements in computers, technology and medical advancements. Many of these medical breakthroughs were in other countries however, there have been many notable advancements done in the US. During the 1900s medical advancement was growing rapidly. Sultz and Young (2018) states that some of the most mentionable advancements consisted of:
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The development of vaccines.
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The end of poliomyelitis epidemics using Sabin and Salk vaccines.
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The introduction and use of Librium and Valium. Tranquilizers that were prescribed for emotional and physically illness.
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Advancements in contraceptive methods through the first prescription birth control pill.
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The heart–lung machine and major improvements in the efficacy and safety of general anesthesia techniques made possible the first successful heart bypass operation in 1964.
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in 1972, computed tomography was invented
(P.29 )
There was also the use of diagnostic imaging advancements. The use of MRI and CT scans swept through the hospitals of the nation. With this new technology came the development and use of new drugs and medical procedures. Consequently, with the new technologies came longer life expectancy. There was no shortage in complications that arose from these new advancements. Ethical and financial issues rose to the surface causing a need for exploration. According to Sultz and Young (2018), “The AMA established three programs to assess the ramifications of medical advancements: the Diagnostic and Therapeutic Technology Assessment Program, the Council on Scientific Affairs, and the AMA Drug Evaluations.”(P.29) Once these issues were brought to light to policy makers there was a need for them to be addressed. This is what Congress did with the Technology Assessment Act of 1972. “Congress recognized that “it is essential that, to the fullest extent possible, the consequences of technologic applications be anticipated, understood, and considered in determination of public policy on existing and emerging national problems.” (Sultz & Young, 2018, P.29) The Office of Technological Assessment was birthed and was intended to sort out complex information while being unbiased. 1995 was the end of the OTC due to controversies within Congress. That wasn’t the only program introduced to support research within the healthcare system. The Agency for Health Care Policy and Research was brought about in 1989. It’s aim was to get a better understanding of healthcare and healthcare outcomes on a clinical and systems level. The research was to get a sense of what worked. (Sultz & Young,2018, P.30)
Other influences on healthcare
There are four other notable influences on US healthcare. The first is the Health Insurance Portability and Accountability Act, also known as HIPPA. HIPPA was enacted in 1996 with two main purposes in mind, uninterrupted health insurance coverage when a change in employment or a change in family composition. The second main purpose and most well known is personal health information privacy. The need to maintain patient confidentiality has extended into third parties who have access to patient health records. According to Sultz and Young (2018), “In 2013 DHHS issued final rules under a 2009 law that significantly extended HIPAA’s Privacy and Security provisions beyond healthcare organizations and providers to their subcontractors and other business entities which handle electronic patient information. The DHHS Office of Civil Rights has responsibility for enforcing the Privacy and Security Rules with voluntary compliance activities and civil money penalties.”(P.33) Keeping patient’s privacy has been a huge focus in healthcare since 1996 with trainings, updates and enforcement.
The second notable influence on US healthcare is the Oregon Death with Dignity Act and Other End-of-Life Legislation. Enacted in 1994, this act made it legal for those who are terminally within the state of Oregon to request an assisted suicide. This would be done by a physician prescribing a prescription that would end the patient’s life. Some states in following years would follow in the footsteps of Oregon with similar legislation. Washington followed in 2008, Montana in 2010, Vermont in 2013, California in 2016. Deliberations in some states are still going, such as New Mexico. (Sultz & Young, 2018, P.35)
The third notable influence is the Health Information Technology for Economic and Clinical Health Act. According to Sultz and Young, (2018), “The federal government took the most significant step in the history of health information technology on April 27, 2004, when President Bush created the Office of the National Coordinator for Health Information Technology (ONCHIT or “the ONC”) by Executive Order. The ONC was legislatively mandated in the American Recovery and Reinvestment Act (ARRA) when signed by President Obama on February 17, 2009.”(P.35) This was when the use of EHRs was mandated as it was part of the ARRA through the Health Information Technology for economic and Clinical Health Act. With the use of EHR’s HIPPA becomes more important and pushes the need for security.
The fourth notable influence is the internet. The availability of information is astounding, and patients can look up their symptoms and educate themselves about their potential condition prior to ever seeing their physician. This can expedite the appointment and at times can make it longer. The use of the internet extends into healthcare facilities. Payment systems, referrals systems, EHRs all use the internet to be efficient. Use of portable electronics are being implemented to obtain some intake information on the patient before being taken to an exam room.
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US healthcare has been a fast-moving evolution due to new discoveries and advancements but in other areas has been a continuous cycle to try and fix. The history of US healthcare is vast and will continue to grow and change throughout time. There are many politics, organizations, technologies and advancements that will help oversee many changes. Learning about the history can better help form the future.

Resources:
Penn in the 18th Century School of Medicine. (2019). Retrieved October 2, 2019, from https://archives.upenn.edu/exhibits/penn-history/18th-century/medical-school.
Young, K. M., Kroth, P. J., & Sultz, H. A. (2018). Sultz & Youngs health care Usa: understanding its organization and delivery. Burlington, MA: Jones & Bartlett Learning.
US healthcare has evolved since its beginning with the founding of our country. Medical care started in the Colonial era and was very simple with the system involving two parties. Through many changes, innovations, discoveries and the introduction of third parties into the healthcare system it has evolved into what we see in America today. This evolution of change has brought about favorable outcomes but has also led to unfavorable outcomes within the healthcare system. Through this history of change we can see how healthcare has evolved to where it is today.
