- Joined
- Nov 21, 1998
- Messages
- 12,564
- Reaction score
- 6,955
See attached.
Observations on CDC Guideline for Prescribing Opioids – United States, 2022
This document outlines the observations of the Opioid Workgroup on the updated CDC Guideline for Prescribing
Opioids. CDC recommendations for prescribing opioids for outpatients with pain outside of sickle cell disease-related
pain management, cancer pain treatment, palliative care, and end-of-life care. The observations presented here follow
the ordering of the draft Guideline.
Overall Observations
Overarching Themes
• Overall, many workgroup members felt that much of the supporting text of the guideline was not balanced and was
missing key studies. Many workgroup members felt that the guideline focused heavily on the risks or potential
harms of opioids, while less attention was focused on the potential benefits of opioids, or the risk of not taking
opioids or undertreating pain. In addition, some workgroup members felt that the language of the recommendation
statements or supporting text conveyed more certainty or was more absolute than warranted by the evidence.
• Much of the discussion of the recommendations centered around the concern for misapplication of the guideline.
Because of the consequences of misapplication of the 2016 guideline, many workgroup members were concerned
about how the recommendation could be misapplied, leading to potential harm to patients. The workgroup
discussion thus focused on how best to mitigate against this valid concern while preserving the benefits of the
guideline. However, some were concerned that the workgroup may have been over-correcting and so much concern
about future misapplication could potentially be detrimental to the greater good.
• Many workgroup members felt the guideline paid too little attention and had minimal discussion about racial/ethnic
disparities and inequities in how pain is perceived, valued, and managed, and the potential implications of these
disparities on implementation of the guideline, including disparities in access to recommended treatments, along
with how the guideline could impact disparities.
• Many workgroup members noted how the guideline has a constant tension between public health benefits versus
patient benefits. This issue is minimally addressed in the guideline and comes very late. Workgroup members felt it
is important to directly address this tension between risks and benefits to public health versus individual patients,
and to contextualize how individual providers should use this guideline in caring for their patients versus considering
potential public health consequences. In addition, several workgroup members felt that overall, the guideline was
not sufficiently patient-centered.
• Many workgroup members were cautious about including specific opioid dose thresholds in the recommendations.
Workgroup members acknowledged the importance of having benchmarks, but many felt that specific opioid doses
would be misapplied as absolute cutoffs or thresholds for policies or practices. Many workgroup members felt the
specific opioid dose thresholds belonged in the supporting text where the discussion could be more nuanced. In
addition, there is no single standard formula for calculating MMEs.
• Many workgroup members noted a sense of exceptionalism throughout the guideline. Specifically, certain
conditions were named in the text, while others were not. Naming of specific conditions may lead to interpretation
regarding whether pain is “real” or “worthy” of certain types of treatment. In addition, while the guideline states it
does not apply to sickle cell disease, cancer, palliative care, or end-of-life care, palliative care is not clearly defined.
• Many workgroup members felt that the recommendation category A was overutilized (11 of the 12 statements had
recommendation category A). Members felt that this type of grading likely contributed to the misapplication of the
2016 guideline.
• Many members of the workgroup developed a document that described the workgroup’s guiding principles when
providing observations on the guideline. Guiding principles include: minimize bias, ensure scientific integrity,
enhance inclusivity, establish patient- and clinician-centered guidance, and mitigate harms from unintended
consequences. The document is included as Appendix A.
Observations on CDC Guideline for Prescribing Opioids – United States, 2022
This document outlines the observations of the Opioid Workgroup on the updated CDC Guideline for Prescribing
Opioids. CDC recommendations for prescribing opioids for outpatients with pain outside of sickle cell disease-related
pain management, cancer pain treatment, palliative care, and end-of-life care. The observations presented here follow
the ordering of the draft Guideline.
Overall Observations
Overarching Themes
• Overall, many workgroup members felt that much of the supporting text of the guideline was not balanced and was
missing key studies. Many workgroup members felt that the guideline focused heavily on the risks or potential
harms of opioids, while less attention was focused on the potential benefits of opioids, or the risk of not taking
opioids or undertreating pain. In addition, some workgroup members felt that the language of the recommendation
statements or supporting text conveyed more certainty or was more absolute than warranted by the evidence.
• Much of the discussion of the recommendations centered around the concern for misapplication of the guideline.
Because of the consequences of misapplication of the 2016 guideline, many workgroup members were concerned
about how the recommendation could be misapplied, leading to potential harm to patients. The workgroup
discussion thus focused on how best to mitigate against this valid concern while preserving the benefits of the
guideline. However, some were concerned that the workgroup may have been over-correcting and so much concern
about future misapplication could potentially be detrimental to the greater good.
• Many workgroup members felt the guideline paid too little attention and had minimal discussion about racial/ethnic
disparities and inequities in how pain is perceived, valued, and managed, and the potential implications of these
disparities on implementation of the guideline, including disparities in access to recommended treatments, along
with how the guideline could impact disparities.
• Many workgroup members noted how the guideline has a constant tension between public health benefits versus
patient benefits. This issue is minimally addressed in the guideline and comes very late. Workgroup members felt it
is important to directly address this tension between risks and benefits to public health versus individual patients,
and to contextualize how individual providers should use this guideline in caring for their patients versus considering
potential public health consequences. In addition, several workgroup members felt that overall, the guideline was
not sufficiently patient-centered.
• Many workgroup members were cautious about including specific opioid dose thresholds in the recommendations.
Workgroup members acknowledged the importance of having benchmarks, but many felt that specific opioid doses
would be misapplied as absolute cutoffs or thresholds for policies or practices. Many workgroup members felt the
specific opioid dose thresholds belonged in the supporting text where the discussion could be more nuanced. In
addition, there is no single standard formula for calculating MMEs.
• Many workgroup members noted a sense of exceptionalism throughout the guideline. Specifically, certain
conditions were named in the text, while others were not. Naming of specific conditions may lead to interpretation
regarding whether pain is “real” or “worthy” of certain types of treatment. In addition, while the guideline states it
does not apply to sickle cell disease, cancer, palliative care, or end-of-life care, palliative care is not clearly defined.
• Many workgroup members felt that the recommendation category A was overutilized (11 of the 12 statements had
recommendation category A). Members felt that this type of grading likely contributed to the misapplication of the
2016 guideline.
• Many members of the workgroup developed a document that described the workgroup’s guiding principles when
providing observations on the guideline. Guiding principles include: minimize bias, ensure scientific integrity,
enhance inclusivity, establish patient- and clinician-centered guidance, and mitigate harms from unintended
consequences. The document is included as Appendix A.
Attachments
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