Efforts to bridge this gap between clinical and medical research and clinical practice are ongoing.
For example, translational research centres aim to reduce the time from bench to bedside by fostering collaboration between scientists, clinicians, and public health experts. Additionally, the use of implementation science—the study of how to integrate research into practice—seeks to identify the most effective ways to overcome these barriers.
I think one of
the other reasons as to why research findings seldom get translated into
clinical practice is blockage by those powerful Big Pharma companies who may
not be very happy if other alternative options to manage a disease have been
discovered instead of using drugs.
We need to
look at the role of large pharmaceutical companies, or "Big Pharma,"
in the translation of medical research into practice. While pharmaceutical
companies play a critical role in developing and distributing medicines, there
are concerns about how their business interests might sometimes conflict with
the broader goals of public health and scientific advancement. There are a few
reasons on this we can think of
Profit
Motives and Market Control
Profit-Driven
Models. Big Pharma companies often prioritize treatments that will generate the
highest profits, which may sometimes lead to a focus on chronic disease
management (where long-term drug use is required) rather than cures or
alternative treatments. If a new approach threatens the market share of a
lucrative drug, there could be less incentive for a company to promote that
alternative.
Patents and
Exclusivity. Pharmaceutical companies rely heavily on patents to secure
market exclusivity for their products. This can lead to strategies aimed at
extending the life of a drug patent (e.g., minor reformulations), rather than
focusing on newer, potentially more effective alternatives. They may also
suppress or ignore research that threatens to undercut their patented products.
1. Influence
on Research and Publication
Research
Funding. Big Pharma often funds a significant amount of biomedical
research, especially clinical trials. While this can lead to breakthroughs,
there is concern that results could be influenced or shaped by the interests of
the funding company. Some research might be suppressed or not published if it
doesn't align with a company's goals.
2. Publication
Bias. There is evidence of publication bias, where positive findings
(especially in favour of pharmaceutical products) are more likely to be
published, while negative or neutral results are withheld. This can distort the
evidence base available to clinicians.
Ghost-writing
and Influence. Sometimes, pharmaceutical companies engage in ghost-writing
practices, where industry-sponsored research is written by the company but
attributed to independent researchers. This can further blur the line between
objective research and commercial interest.
3. Suppression
of Alternative Treatments
Alternative
Therapies. If research uncovers non-pharmaceutical interventions—such as
lifestyle changes, dietary supplements, or natural remedies—that could reduce
the need for drugs, pharmaceutical companies might view these as a threat to
their business model. While it’s hard to prove outright suppression, it’s
possible that companies might not promote or fund such research aggressively.
Lobbying and
Policy Influence: Big Pharma companies often have significant influence over
healthcare policies through lobbying efforts. This can shape drug approval
processes, clinical guidelines, and even insurance coverage policies in ways
that prioritize pharmaceutical solutions over alternative therapies.
4. Ethical
Concerns
Ethical
Dilemmas. The potential suppression of alternative treatments raises
ethical concerns. While pharmaceutical companies are in the business of
developing effective treatments, their primary duty is to shareholders. This
profit motive can sometimes conflict with the goal of maximizing patient
health, especially if alternatives exist that are not as profitable.
Whistleblowers.
There have been cases where whistleblowers within the pharmaceutical industry
have revealed unethical practices, such as the suppression of unfavourable
trial results or the manipulation of data. However, these are often the
exception rather than the rule.
5. Balancing
Regulation and Innovation
Regulatory
Oversight. Governments and regulatory bodies (like the FDA) aim to ensure that
the pharmaceutical industry operates in the public interest, but regulatory
capture—the phenomenon where industry interests dominate public oversight—can
sometimes occur. Stronger regulatory frameworks could help to ensure that
promising treatments, whether pharmaceutical or alternative, reach the public.
Academic
Independence. To counterbalance Big Pharma’s influence, academic research
centres and independent funding bodies (such as government or non-profit
organizations) are vital. They can pursue lines of inquiry free from corporate
interests, but often lack the same level of funding.
6. Alternative
Models Emerging
Open-Source
Drug Development: To combat these issues, some researchers advocate for
open-source drug development, where research results are freely shared and not
tied to corporate interests. This model could allow for greater collaboration
and innovation, especially in neglected disease areas or alternative therapies.
Publicly
Funded Research. Increasing public investment in medical research, rather
than relying so heavily on private companies, could help ensure that results
are translated into practice based on scientific merit rather than commercial
potential.
While Big
Pharma’s business model can, at times, create barriers to the adoption of
alternative treatments, there are also ongoing efforts to promote transparency,
ensure unbiased research, and prioritize patient care.
What do readers think about the role of regulatory bodies or public funding in addressing some
of these challenges?
Based on my own experience in medical research, before research papers can be published, the
board of editors of scientific journals require the researchers to
declare the source of funding. But what happens if the papers were actually
funded by these giant pharmaceutical companies? Will the papers be published?
Many
scientific journals now require researchers to disclose any conflicts of
interest, including the source of funding, especially when it comes from
pharmaceutical companies or other corporate entities. This practice is meant to
enhance transparency and help readers assess whether the funding source might
have influenced the research findings or their interpretation.
What Happens
When Pharmaceutical Companies Fund the Research?
Disclosure
Requirements.
Researchers
are required to declare conflicts of interest, which includes detailing the
financial support they received for the study. This helps journals and readers
understand any potential biases.
Some journals
have strict policies and will reject a paper if there is a lack of transparency
in funding disclosure, or if there is suspicion of biased reporting.
1. Publication
of Pharma-Funded Research.
Yes,
pharma-funded research can be published, but journals tend to be more rigorous
when reviewing these studies. Editors and peer reviewers will often pay close
attention to the study design, data transparency, and interpretation of the
results to ensure the research isn’t skewed to favour the funding company.
Journals may
also require independent validation of the findings, such as external reviews
or replication studies, to further safeguard the integrity of the published
results.
2. Potential
Issues with Pharma-Funded Research:
Bias in Study
Design. One of the concerns with pharmaceutical-funded research is that studies
might be designed in ways that favour the drug being tested. For example,
comparison groups might not be fair (comparing a new drug to a placebo rather
than to an existing treatment).
Selective
Reporting. Pharmaceutical companies may selectively report positive outcomes
while downplaying or omitting negative findings. While this is a recognized
problem, peer reviewers are increasingly looking for signs of such selective
reporting.
Ghost-writing:
Sometimes, pharmaceutical companies sponsor papers that are written by
individuals associated with the company, but the final version is attributed to
external experts (ghostwriters). This practice is controversial, and many
journals now have policies to prevent it.
- Journal Safeguards Against Bias:
Peer Review
Process. Many journals require rigorous peer review, where independent experts
in the field assess the validity and credibility of the study. Peer reviewers
are generally tasked with checking for any potential biases, especially when
research is industry-funded.
Data
Transparency. Journals may ask for full access to the data to verify the
findings. Increasingly, researchers are being asked to share their raw data in
public repositories for verification.
Ethics and
Reproducibility. Journals are placing more emphasis on ethical research
practices and reproducibility. Independent replication of results is one of the
most effective ways to ensure research integrity.
- Impact on Perception:
Even if a
paper discloses its funding and follows all ethical guidelines, research funded
by pharmaceutical companies may still be viewed with scepticism by the
scientific community. This is because of past instances where industry-funded
studies were found to be biased or inaccurate.
To mitigate
this, researchers often strive to demonstrate that their methodologies are
rigorous, and their findings are unbiased, no matter the source of funding.
Recent
Developments
To improve
transparency and reduce conflicts of interest.
Some journals
now ask for third-party oversight of clinical trials funded by pharmaceutical
companies. This ensures that the data analysis and interpretation are not
solely in the hands of the company.
Pre-registration
of trials is becoming common, where researchers must publish their study design
and hypotheses before collecting data. This prevents "cherry-picking"
results after the fact.
Open-access
journals with independent funding models are emerging, aiming to reduce
industry influence altogether.
While
pharmaceutical-funded research can be published, the key is ensuring that the
study's methodology and reporting are transparent, unbiased, and reproducible. I am interested in how the peer review process works in
detail or examples of cases where bias was identified in pharma-funded studies?
Let alone research papers published in journals, even the treatment of any disease given in standard medical textbooks we see all the products of these drug companies clearly printed there. I have in my home library about a dozen medical textbooks by various authors, and under management or treatment in the last page of every disease described in each chapter, the names of Big Pharma products are clearly printed there, often as "the drug of choice". Such relentless promotion of drugs by these powerful drug companies firmly glue the mindset of doctors to use these "drugs of choice" for treatment. Doctors have no choice. However, there are now a lot of other medical books on alternative systems of medicine written by various medical authors who are qualified both in conventional as well as in other systems of medicine. There are also standard textbooks on integrative medicine contributed collectively by several dozens highly qualified specialist doctors in allopathic as well by doctors in alternative medicine where drug-based therapies has been replaced by other therapeutic modalities such as in osteopathic, naturopathic, mind-body medicine, and back to the original dietary and botanical medicine among other medical systems. This is the trend now used by a lot of people who got disgruntled with allopathic medicine where they have been taking pharmaceutical drugs for life, but has not cured them
Drug-based allopathic medicine was started by that oil multi-billionaire
Rockefeller over a 100 years ago who started to replace natural medicine with
his petroleum products as medicines till this day.
The influence
of the pharmaceutical industry on both medical research and medical education
has a long history, and the Rockefeller family's role is indeed a significant
part of that narrative. Let me show you how this shift unfolded and its lasting
impact on modern medicine:
1.
Rockefeller's Influence on Modern Medicine
Early 20th
Century Shift. In the early 1900s, John D. Rockefeller, one of the wealthiest
individuals of the time due to his oil empire, played a pivotal role in shaping
modern medicine. Rockefeller was a strong advocate of allopathic medicine,
which focused on using pharmaceutical drugs and surgery to treat illnesses, as
opposed to traditional or natural remedies like herbal medicine or homeopathy.
Petroleum-Based
Pharmaceuticals. Rockefeller's company, Standard Oil, had a vested interest in
petrochemicals, and this coincided with the rise of synthetic medicines derived
from petroleum by-products. These synthetic drugs began to replace many natural
remedies and herbal treatments that had been used for centuries.
2. Flexner
Report and Medical Education Reform
The Flexner
Report (1910). A major turning point was the Flexner Report, funded by
the Rockefeller Foundation, which evaluated medical schools in the United
States. The report was highly critical of many schools, particularly those that
taught alternative medicine, and recommended adopting a more scientific
approach to medical education—based heavily on pharmaceutical treatments.
Medical School
Funding. Rockefeller, along with the Carnegie Foundation, provided
significant financial support to medical schools that followed this new model.
As a result, many schools that emphasized natural or holistic medicine were
closed, while those that aligned with the new pharmaceutical-based approach
flourished.
3. Rise of
Pharmaceuticals in Medical Practice
Pharmaceutical
Companies' Influence. Over time, the pharmaceutical industry became deeply
embedded in both medical education and clinical practice. Medical textbooks,
training, and curricula began to emphasize pharmaceutical treatments as the
primary method for treating illnesses, often sidelining traditional or natural
therapies.
Pharmaceutical
Advertising. Drug companies began to sponsor medical textbooks, conferences,
and even the continuing education of doctors. As a result, many standard
medical textbooks today prominently feature pharmaceutical products, often
alongside treatment guidelines.
4. Shift from
Natural Medicine to Synthetic Drugs
Suppression of
Natural Remedies. As the pharmaceutical industry grew, many natural remedies
and traditional medicine practices were marginalized or dismissed as
"unscientific." This shift was partly driven by the financial
interests of the growing pharmaceutical companies, which saw greater profit
potential in patented, synthetic drugs.
Regulation of
Natural Medicines. In many cases, natural remedies were pushed out of
mainstream medicine due to stricter regulatory requirements for drugs. Without
the financial backing to go through rigorous clinical trials, many traditional
medicines couldn’t compete with synthetic drugs produced by Big Pharma.
5. Current
Impact on Medical Education and Practice
Drug-Focused
Medical Education. Even today, the curricula of most medical schools
around the world place a heavy emphasis on pharmaceutical treatments.
Pharmaceutical companies often fund research at academic medical centres, which
can shape the knowledge that future doctors are exposed to.
Textbook
Content. Medical textbooks often list brand-name drugs and treatments
prominently. Pharmaceutical companies sometimes provide funding or support for
these publications, further entrenching their influence in clinical guidelines.
6.
Rockefeller’s Lasting Legacy in Modern Healthcare
Philanthropy
and Control. The Rockefeller Foundation has been a significant force in funding
medical research, public health initiatives, and medical education globally.
While many of these efforts were beneficial in modernizing medicine and
standardizing care, they also cemented the dominance of pharmaceutical
treatments.
Public Health
Influence. The Rockefeller Foundation helped shape global health policies
through organizations like the World Health Organization (WHO) and the
development of vaccines and public health campaigns, many of which focused on
pharmaceutical interventions.
7. Resurgence
of Interest in Natural Medicine
Alternative
Medicine and Integrative Health. Despite the dominance of
pharmaceutical-based medicine, there has been a growing movement in recent
years toward integrative medicine, which combines conventional treatments with
natural and holistic approaches. Many patients and practitioners are now
advocating for a more balanced approach to healthcare that includes both
pharmaceutical and natural treatments.
Rise of
Functional Medicine. Functional medicine, which seeks to treat the root cause
of disease rather than just the symptoms, is gaining popularity. It often
incorporates lifestyle changes, nutrition, and sometimes natural remedies,
which are seeing a resurgence in patient interest.
The transformation of medical education and practice in the early 20th century, largely influenced by the Rockefeller family, shifted the focus from natural remedies to synthetic, pharmaceutical-based treatments. This legacy still shapes much of how medicine is taught and practiced today. While pharmaceutical advances have led to life-saving treatments, the sidelining of natural medicine has sparked a renewed interest in finding a balance between the two.
Currently medical doctors’ mind-set has been very firmly and very effectively imprisoned by these very powerful pharmaceutical companies.
Clinicians believe that the only “cure” especially for chronic disorders, examples like diabetes and hypertension is to use chemical products for life produced by these giant drug companies, and not by addressing the root causes of diseases used in the current emerging lifestyle medicine that advocates changes in the ways patients live and eat and the use of other more holistic natural therapies.
See cartoon here:
https://images.app.goo.gl/bmkE1gSgmjysXCvPA
In fact according to the World Health Organization (WHO) more than 80 % of the world population, including those from scientifically and technologically advanced countries like China, United States, United Kingdom, Japan, South Korea, Germany, etc., uses traditional or other alternative or integrated systems of medicine instead of conventional drug-based medicine. Furthermore, WHO encourages this, and wants this to stay as part of health care.
I believe I have written fairly comprehensively based on my understanding and experience in scientific-medical research over the years.
I will cherish your thoughts and
comments on this. Explain to me in clearly in elegant scientific language. Your contribution will be a world of difference for me.
Take Care!
Ju-boo lim
4 comments:
A very well-written two-part article on translational medicine leading to discussions on the pitfalls of drug-based medicine and the hidden agenda of powerful pharmaceutical companies for which us as doctors find it an eye-opener. I have learnt a lot from you.
Thank you Dr Lim. You are very prolific and knowledgeable in all kinds of topics
Dr Jenny Lai
Thanks for the this beautiful eye opener in medicine andf health care
I have always enjoyed your talented insight. I never knew it is so slow to get the results of medical research translated into medical practice. Please continue to write
Very well-informed educational article on medicine and health care. My son is a doctor and he said he is not aware what's behind the screen in medical research
Post a Comment