After the authors of the PACE trial brushed off Tuller's observation that conflicts of interest were not reported to trial participants, he did some research. Predictably, he found that not only were three of the four principal researchers hired as consultants for insurance companies, but that decisions made by those companies had direct bearing on PACE findings and on recommendations made by PACE authors.
Corporate Collusion?
Conflicts of interest have become a major problem in the medical field. With pharmaceutical and insurance companies hiring physicians and researchers to conduct and evaluate basic research, the results of those studies have become increasingly unreliable.
It was the editor of The Lancet, Richard Horton, who observed that half of the research published was false. In a May 2015 editorial he stated that:
“The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness.” [Emphasis mine]
The irony of this statement cannot be lost on those who have followed the PACE trial.
Some of the main players in the push to have ME/CFS labeled as a psychiatric illness have advised insurance companies. These companies have consistently used this medical advice and "research" to turn down disability and medical claims. (For an excellent article on this topic as it relates to ME/CFS, read Corporate Collusion?)
Michael Sharpe, a principal investigator for PACE, provided expert testimony and advice to several insurance companies, including UNUM Provident, Windsor Life, Bupa, Reassure, and Aegon UK.
Dr. Peter Manu, a psychiatrist employed as a consultant with Metlife, was instrumental in securing denials of disability payments to patients with CFS. In a chapter published in Disability and Chronic Fatigue Syndrome he argued that patients with CFS are really suffering from psychiatric illnesses, but are misdiagnosed by physicians who express "strong convictions" that CFS is produced by an immune dysfunction, a virus, or "other physical cause."
Dr. Manu went on to write a book, The Psychopathology of Functional Somatic Syndromes: Neurobiology and Illness Behavior in Chronic Fatigue Syndrome, Fibromyalgia, Gulf War Illness, Irritable Bowel, and Premenstrual Dysphoria, in which he argues that all of the aformentioned are psychosomatic. (Manu drew liberally upon Sharpe to defend his statement that "most physicians have understood [these conditions] to be mental illnesses.") His recommendation was to treat the illnesses with antidepressants and CBT.
ME/CFS is not the only illness that has been the object of insurance company manipulation. As a case in point, the existence of Chronic Lyme disease has been consistently denied by the IDSA (Infectious Diseases Society of America), an organization whose ties to industry led to an investigation by the Connecticut Attorney General. The investigation concluded that "The conflicts of interest of the IDSA guidelines panel members were significant and represent the type of ties to industry and patents that are common to key academic researchers in the field."
David Tuller has done an excellent job of exposing some of the industry ties that formed the rationale for, and determined the results of, the PACE trial. It is up to us to insist on an investigation.
You can sign the petition to retract the PACE trial HERE.
You can sign the petition demanding an HHS investigation of the PACE trial HERE.
________________________________
ME/CFS is not the only illness that has been the object of insurance company manipulation. As a case in point, the existence of Chronic Lyme disease has been consistently denied by the IDSA (Infectious Diseases Society of America), an organization whose ties to industry led to an investigation by the Connecticut Attorney General. The investigation concluded that "The conflicts of interest of the IDSA guidelines panel members were significant and represent the type of ties to industry and patents that are common to key academic researchers in the field."
David Tuller has done an excellent job of exposing some of the industry ties that formed the rationale for, and determined the results of, the PACE trial. It is up to us to insist on an investigation.
You can sign the petition to retract the PACE trial HERE.
You can sign the petition demanding an HHS investigation of the PACE trial HERE.
________________________________
THIS ARTICLE ORIGINALLY APPEARED ON VIROLOGY BLOG
Trial by Error, Continued: PACE Team’s Work for Insurance Companies Is “Not Related” to PACE. Really?
By David Tuller, Wednesday, November 18, 2015 at 06:45 AM EST
In my initial story on Virology Blog, I charged the PACE investigators with violating the Declaration of Helsinki, developed in the 1950s by the World Medical Association to protect human research subjects. The declaration mandates that scientists disclose "institutional affiliations" and "any possible conflicts of interest" to prospective trial participants as part of the process of obtaining informed consent.
The investigators promised in their protocol to adhere to this foundational human rights document, among other ethical codes. Despite this promise, they did not tell prospective participants about their financial and consulting links with insurance companies, including those in the disability sector. That ethical breach raises serious concerns about whether the "informed consent" they obtained from all 641 of their trial participants was truly "informed," and therefore legitimate.
The PACE investigators do not agree that the lack of disclosure is an ethical breach. In their response to my Virology Blog story, they did not even mention the Declaration of Helsinki or explain why they violated it in seeking informed consent. Instead, they defended their actions by noting that they had disclosed their financial and consulting links in the published articles, and had informed participants about who funded the research--responses that did not address the central concern.
"I find their statement that they disclosed to The Lancet but not to potential subjects bemusing," said Jon Merz, a professor of medical ethics at the University of Pennsylvania. "The issue is coming clean to all who would rely on their objectivity and fairness in conducting their science. Disclosure is the least we require of scientists, as it puts those who should be able to trust them on notice that they may be serving two masters."
In their Virology Blog response, the PACE team also stated that no insurance companies were involved in the research, that only three of the 19 investigators "have done consultancy work at various times for insurance companies," and that this work "was not related to the research." The first statement was true, but direct involvement in a study is of course only one possible form of conflict of interest. The second statement was false. According to the PACE team's conflict of interest disclosures in The Lancet, the actual number of researchers with insurance industry ties was four—along with the three principal investigators, physiotherapist Jessica Bavington acknowledged such links.
But here, I'll focus on the third claim--that their consulting work "was not related to the research." In particular, I'll examine an online article posted by Swiss Re, a large reinsurance company. The article describes a "web-based discussion group" held with Peter White, the lead PACE investigator, and reveals some of the claims-assessing recommendations arising from that presentation. White included consulting work with Swiss Re in his Lancet disclosure.
The Lancet published the PACE results in February, 2011; the undated Swiss Re article was published sometime within the following year or so. The headline: "Managing claims for chronic fatigue the active way." (Note that this headline uses "chronic fatigue" rather than "chronic fatigue syndrome," although chronic fatigue is a symptom common to many illnesses and is quite distinct from the disease known as chronic fatigue syndrome. Understanding the difference between the two would likely be helpful in making decisions about insurance claims.)
The Swiss Re article noted that the illness "can be an emotive subject" and then focused on the implications of the PACE study for assessing insurance claims. It started with a summary account of the findings from the study, reporting that the "active rehabilitation" arms of cognitive behavioral therapy and graded exercise therapy "resulted in greater reduction of patients' fatigue and larger improvement in physical functioning" than either adaptive pacing therapy or specialist medical care, the baseline condition. (The three intervention arms also received specialist medical care.)
The trial's "key message," declared the article, was that "pushing the limits in a therapeutic setting using well described treatment modalities is more effective in alleviating fatigue and dysfunction than staying within the limits imposed by the illness traditionally advocated by ‘pacing.'"
Added the article: "If a CFS patient does not gradually increase their activity, supported by an appropriate therapist, then their recovery will be slower. This seems a simple message but it is an important one as many believe that ‘pacing' is the most beneficial treatment."
This understanding of the PACE research—presumably based on information from Peter White's web-based discussion—was wrong. Pacing is not and has never been a "treatment." It is also not one of the "four most commonly used therapies," as the newsletter article declared, since it has never been a "therapy" either. It is a self-help method practiced by many patients seeking the best way to manage their limited energy reserves.
The PACE investigators did not test pacing. Instead, the intervention they dubbed "adaptive pacing therapy" was an operationalized version of "pacing" developed specifically for the study. Many patients objected to the trial's form of pacing as overly prescriptive, demanding and unlike the version they practiced on their own. Transforming an intuitive, self-directed approach into a "treatment" administered by a "therapist" was not a true test of whether the self-help approach is effective, they argued--with significant justification. Yet the Swiss Re article presented "adaptive pacing therapy" as if it were identical to "pacing."
The Swiss Re article did not mention that the reported improvements from "active rehabilitation" were based on subjective outcomes and were not supported by the study's objective data. Nor did it report any of the major flaws of the PACE study or offer any reasons to doubt the integrity of the findings.
The article next asked, "What can insurers and reinsurers do to assist the recovery and return to work of CFS claimants?" It then described the conclusions to be drawn from the discussion with White about the PACE trial—the "key takeaways for claims management."
First, Swiss Re advised its employees, question the diagnosis, because "misdiagnosis is not uncommon."
The second point was this: "It is likely that input will be required to change a claimant's beliefs about his or her condition and the effectiveness of active rehabilitation...Funding for these CFS treatments is not expensive (in the UK, around £2,000) so insurers may well want to consider funding this for the right claimants."
Translation: Patients who believe they have a medical disease are wrong, and they need to be persuaded that they are wrong and that they can get better with therapy. Insurers can avoid large payouts by covering the minimal costs of these treatments for patients vulnerable to such persuasion, given the right "input."
Finally, the article warned that private therapists might not provide the kinds of "input" required to convince patients they were wrong. Instead of appropriately "active" approaches like cognitive behavior therapy and graded exercise therapy, these therapists might instead pursue treatments that could reinforce claimants' misguided beliefs about being seriously ill, the article suggested.
"Check that private practitioners are delivering active rehabilitation therapies, such as those described in this article, as opposed to sick role adaptation," the Swiss RE article advised. (The PACE investigators, drawing on the concept known as "the sick role" in medical sociology, have long expressed concern that advocacy groups enabled patients' condition by bolstering their conviction that they suffered from a "medical disease," as Michael Sharpe, another key PACE investigator, noted in a 2002 UNUMProvident report. This conviction encouraged patients to demand social benefits and health care resources rather than focus on improving through therapy, Sharpe wrote.)
Lastly, the Swiss Re article addressed "a final point specific to claims assessment." A diagnosis of chronic fatigue syndrome, stated the article, provided an opportunity in some cases to apply a mental health exclusion, depending upon the wording of the policy. In contrast, a diagnosis of myalgic encephalomyelitis did not.
The World Health Organization's International Classification for Diseases, or ICD, which clinicians and insurance companies use for coding purposes, categorizes myalgic encephalomyelitis as a neurological disorder that is synonymous with the terms "post-viral fatigue syndrome" and "chronic fatigue syndrome." But the Swiss Re article stated that, according to the ICD, "chronic fatigue syndrome" can also "alternatively be defined as neurasthenia which is in the mental health chapter."
The PACE investigators have repeatedly advanced this questionable idea. In the ICD's mental health section, neurasthenia is defined as "a mental disorder characterized by chronic fatigue and concomitant physiologic symptoms," but there is no mention of "chronic fatigue syndrome" as a discrete entity. The PACE investigators (and Swiss Re newsletter writers) believe that the neurasthenia entry encompasses the illness known as "chronic fatigue syndrome," not just the common symptom of "chronic fatigue."
This interpretation, however, appears to be at odds with an ICD rule that illnesses cannot be listed in two separate places—a rule confirmed in an e-mail from a WHO official to an advocate who had questioned the PACE investigators' argument. "It is not permitted for the same condition to be classified to more than one rubric as this would mean that the individual categories and subcategories were no longer mutually exclusive," wrote the official to Margaret Weston, the pseudonym for a longtime clinical manager in the U.K. National Health Service.
Presumably, after White disseminated the good news about the PACE results at the web-based discussion, Swiss Re's claims managers felt better equipped to help ME/CFS claimants. And presumably that help included coverage for cognitive behavior therapy and graded exercise therapy so that claimants could receive the critical "input" they needed in order to recognize and accept that they didn't have a medical disease after all.
In sum, contrary to the investigators' argument in their response to Virology Blog, the PACE research and findings appear to be very much "related to" insurance industry consulting work. The claim that these relationships did not represent "possible conflicts of interest" and "institutional affiliations" requiring disclosure under the Declaration of Helsinki cannot be taken seriously.
Update 11/17/15 12:22 PM: I should have mentioned in the story that, in the PACE trial, participants in the cognitive behavior therapy and graded exercise therapy arms were no more likely to have increased their hours of employment than those in the other arms. In other words, there was no evidence for the claims presented in the Swiss Re article, based on Peter White's presentation, that these treatments were any more effective in getting people back to work.
The PACE investigators published this employment data in a 2012 paper in PLoS One. It is unclear whether Peter White already knew these results at the time of his Swiss Re presentation on the PACE results.
By David Tuller, Wednesday, November 18, 2015 at 06:45 AM EST
In my initial story on Virology Blog, I charged the PACE investigators with violating the Declaration of Helsinki, developed in the 1950s by the World Medical Association to protect human research subjects. The declaration mandates that scientists disclose "institutional affiliations" and "any possible conflicts of interest" to prospective trial participants as part of the process of obtaining informed consent.
The investigators promised in their protocol to adhere to this foundational human rights document, among other ethical codes. Despite this promise, they did not tell prospective participants about their financial and consulting links with insurance companies, including those in the disability sector. That ethical breach raises serious concerns about whether the "informed consent" they obtained from all 641 of their trial participants was truly "informed," and therefore legitimate.
The PACE investigators do not agree that the lack of disclosure is an ethical breach. In their response to my Virology Blog story, they did not even mention the Declaration of Helsinki or explain why they violated it in seeking informed consent. Instead, they defended their actions by noting that they had disclosed their financial and consulting links in the published articles, and had informed participants about who funded the research--responses that did not address the central concern.
"I find their statement that they disclosed to The Lancet but not to potential subjects bemusing," said Jon Merz, a professor of medical ethics at the University of Pennsylvania. "The issue is coming clean to all who would rely on their objectivity and fairness in conducting their science. Disclosure is the least we require of scientists, as it puts those who should be able to trust them on notice that they may be serving two masters."
In their Virology Blog response, the PACE team also stated that no insurance companies were involved in the research, that only three of the 19 investigators "have done consultancy work at various times for insurance companies," and that this work "was not related to the research." The first statement was true, but direct involvement in a study is of course only one possible form of conflict of interest. The second statement was false. According to the PACE team's conflict of interest disclosures in The Lancet, the actual number of researchers with insurance industry ties was four—along with the three principal investigators, physiotherapist Jessica Bavington acknowledged such links.
But here, I'll focus on the third claim--that their consulting work "was not related to the research." In particular, I'll examine an online article posted by Swiss Re, a large reinsurance company. The article describes a "web-based discussion group" held with Peter White, the lead PACE investigator, and reveals some of the claims-assessing recommendations arising from that presentation. White included consulting work with Swiss Re in his Lancet disclosure.
The Lancet published the PACE results in February, 2011; the undated Swiss Re article was published sometime within the following year or so. The headline: "Managing claims for chronic fatigue the active way." (Note that this headline uses "chronic fatigue" rather than "chronic fatigue syndrome," although chronic fatigue is a symptom common to many illnesses and is quite distinct from the disease known as chronic fatigue syndrome. Understanding the difference between the two would likely be helpful in making decisions about insurance claims.)
The Swiss Re article noted that the illness "can be an emotive subject" and then focused on the implications of the PACE study for assessing insurance claims. It started with a summary account of the findings from the study, reporting that the "active rehabilitation" arms of cognitive behavioral therapy and graded exercise therapy "resulted in greater reduction of patients' fatigue and larger improvement in physical functioning" than either adaptive pacing therapy or specialist medical care, the baseline condition. (The three intervention arms also received specialist medical care.)
The trial's "key message," declared the article, was that "pushing the limits in a therapeutic setting using well described treatment modalities is more effective in alleviating fatigue and dysfunction than staying within the limits imposed by the illness traditionally advocated by ‘pacing.'"
Added the article: "If a CFS patient does not gradually increase their activity, supported by an appropriate therapist, then their recovery will be slower. This seems a simple message but it is an important one as many believe that ‘pacing' is the most beneficial treatment."
This understanding of the PACE research—presumably based on information from Peter White's web-based discussion—was wrong. Pacing is not and has never been a "treatment." It is also not one of the "four most commonly used therapies," as the newsletter article declared, since it has never been a "therapy" either. It is a self-help method practiced by many patients seeking the best way to manage their limited energy reserves.
The PACE investigators did not test pacing. Instead, the intervention they dubbed "adaptive pacing therapy" was an operationalized version of "pacing" developed specifically for the study. Many patients objected to the trial's form of pacing as overly prescriptive, demanding and unlike the version they practiced on their own. Transforming an intuitive, self-directed approach into a "treatment" administered by a "therapist" was not a true test of whether the self-help approach is effective, they argued--with significant justification. Yet the Swiss Re article presented "adaptive pacing therapy" as if it were identical to "pacing."
The Swiss Re article did not mention that the reported improvements from "active rehabilitation" were based on subjective outcomes and were not supported by the study's objective data. Nor did it report any of the major flaws of the PACE study or offer any reasons to doubt the integrity of the findings.
The article next asked, "What can insurers and reinsurers do to assist the recovery and return to work of CFS claimants?" It then described the conclusions to be drawn from the discussion with White about the PACE trial—the "key takeaways for claims management."
First, Swiss Re advised its employees, question the diagnosis, because "misdiagnosis is not uncommon."
The second point was this: "It is likely that input will be required to change a claimant's beliefs about his or her condition and the effectiveness of active rehabilitation...Funding for these CFS treatments is not expensive (in the UK, around £2,000) so insurers may well want to consider funding this for the right claimants."
Translation: Patients who believe they have a medical disease are wrong, and they need to be persuaded that they are wrong and that they can get better with therapy. Insurers can avoid large payouts by covering the minimal costs of these treatments for patients vulnerable to such persuasion, given the right "input."
Finally, the article warned that private therapists might not provide the kinds of "input" required to convince patients they were wrong. Instead of appropriately "active" approaches like cognitive behavior therapy and graded exercise therapy, these therapists might instead pursue treatments that could reinforce claimants' misguided beliefs about being seriously ill, the article suggested.
"Check that private practitioners are delivering active rehabilitation therapies, such as those described in this article, as opposed to sick role adaptation," the Swiss RE article advised. (The PACE investigators, drawing on the concept known as "the sick role" in medical sociology, have long expressed concern that advocacy groups enabled patients' condition by bolstering their conviction that they suffered from a "medical disease," as Michael Sharpe, another key PACE investigator, noted in a 2002 UNUMProvident report. This conviction encouraged patients to demand social benefits and health care resources rather than focus on improving through therapy, Sharpe wrote.)
Lastly, the Swiss Re article addressed "a final point specific to claims assessment." A diagnosis of chronic fatigue syndrome, stated the article, provided an opportunity in some cases to apply a mental health exclusion, depending upon the wording of the policy. In contrast, a diagnosis of myalgic encephalomyelitis did not.
The World Health Organization's International Classification for Diseases, or ICD, which clinicians and insurance companies use for coding purposes, categorizes myalgic encephalomyelitis as a neurological disorder that is synonymous with the terms "post-viral fatigue syndrome" and "chronic fatigue syndrome." But the Swiss Re article stated that, according to the ICD, "chronic fatigue syndrome" can also "alternatively be defined as neurasthenia which is in the mental health chapter."
The PACE investigators have repeatedly advanced this questionable idea. In the ICD's mental health section, neurasthenia is defined as "a mental disorder characterized by chronic fatigue and concomitant physiologic symptoms," but there is no mention of "chronic fatigue syndrome" as a discrete entity. The PACE investigators (and Swiss Re newsletter writers) believe that the neurasthenia entry encompasses the illness known as "chronic fatigue syndrome," not just the common symptom of "chronic fatigue."
This interpretation, however, appears to be at odds with an ICD rule that illnesses cannot be listed in two separate places—a rule confirmed in an e-mail from a WHO official to an advocate who had questioned the PACE investigators' argument. "It is not permitted for the same condition to be classified to more than one rubric as this would mean that the individual categories and subcategories were no longer mutually exclusive," wrote the official to Margaret Weston, the pseudonym for a longtime clinical manager in the U.K. National Health Service.
Presumably, after White disseminated the good news about the PACE results at the web-based discussion, Swiss Re's claims managers felt better equipped to help ME/CFS claimants. And presumably that help included coverage for cognitive behavior therapy and graded exercise therapy so that claimants could receive the critical "input" they needed in order to recognize and accept that they didn't have a medical disease after all.
In sum, contrary to the investigators' argument in their response to Virology Blog, the PACE research and findings appear to be very much "related to" insurance industry consulting work. The claim that these relationships did not represent "possible conflicts of interest" and "institutional affiliations" requiring disclosure under the Declaration of Helsinki cannot be taken seriously.
Update 11/17/15 12:22 PM: I should have mentioned in the story that, in the PACE trial, participants in the cognitive behavior therapy and graded exercise therapy arms were no more likely to have increased their hours of employment than those in the other arms. In other words, there was no evidence for the claims presented in the Swiss Re article, based on Peter White's presentation, that these treatments were any more effective in getting people back to work.
The PACE investigators published this employment data in a 2012 paper in PLoS One. It is unclear whether Peter White already knew these results at the time of his Swiss Re presentation on the PACE results.
