23 research outputs found
Politics ahead of patients: The battle between medical and chiropractic professional associations over the inclusion of chiropractic in the American Medicare System
Health care professions struggling for legitimacy, recognition, and market share can become disoriented to their priorities. Health care practitioners are expected to put the interests of patients first. Professional associations represent the interests of their members. So when a professional association is composed of health care practitioners, its interests may differ from those of patients, creating a conflict for members. In addition, sometimes practitionersâ perspectives may be altered by indoctrination in a belief system, or misinformation, so that a practitioner could be confused about the reality of patient needs. Politicians, in attempting to find an expedient compromise, can value a âwinâ in the legislative arena over the effects of that legislation. These forces all figure into the events that led to the acceptance of chiropractic into the American Medicare system. Two health care systems in a political fight lost sight of their main purpose: to provide care to patients without doing harm.
Dans leur recherche de lĂ©gitimitĂ©, de reconnaissance et dâune juste part sur le marchĂ© de la santĂ©, les professionnels de la santĂ© peuvent perdre de vue leurs prioritĂ©s. Ces praticiens doivent donner prĂ©sĂ©ance aux intĂ©rĂȘts des patients tandis que les associations professionnelles reprĂ©sentent ceux de leurs membres. Lorsquâune association professionnelle regroupe des praticiens de la santĂ© cependant, ses intĂ©rĂȘts sâopposent parfois Ă ceux des patients, crĂ©ant ainsi un conflit pour les membres. De plus, les praticiens peuvent ĂȘtre endoctrinĂ©s par un systĂšme de valeurs ou mal informĂ©s, au point de se tromper dans lâĂ©valuation des besoins rĂ©els des patients. De leur cĂŽtĂ©, les politiciens peuvent prĂ©fĂ©rer une « victoire » dans lâarĂšne lĂ©gislative Ă une juste apprĂ©ciation des impacts dâune loi. Ces forces ont toutes participĂ© aux Ă©vĂšnements qui ont menĂ© Ă lâacceptation de la chiropraxie par le systĂšme amĂ©ricain Medicare. Dans cette bataille politique, deux systĂšmes de santĂ© ont nĂ©gligĂ© leur principal objectif : soigner des patients sans leur nuire
Stroke genetics informs drug discovery and risk prediction across ancestries
Previous genome-wide association studies (GWASs) of stroke - the second leading cause of death worldwide - were conducted predominantly in populations of European ancestry(1,2). Here, in cross-ancestry GWAS meta-analyses of 110,182 patients who have had a stroke (five ancestries, 33% non-European) and 1,503,898 control individuals, we identify association signals for stroke and its subtypes at 89 (61 new) independent loci: 60 in primary inverse-variance-weighted analyses and 29 in secondary meta-regression and multitrait analyses. On the basis of internal cross-ancestry validation and an independent follow-up in 89,084 additional cases of stroke (30% non-European) and 1,013,843 control individuals, 87% of the primary stroke risk loci and 60% of the secondary stroke risk loci were replicated (P < 0.05). Effect sizes were highly correlated across ancestries. Cross-ancestry fine-mapping, in silico mutagenesis analysis(3), and transcriptome-wide and proteome-wide association analyses revealed putative causal genes (such as SH3PXD2A and FURIN) and variants (such as at GRK5 and NOS3). Using a three-pronged approach(4), we provide genetic evidence for putative drug effects, highlighting F11, KLKB1, PROC, GP1BA, LAMC2 and VCAM1 as possible targets, with drugs already under investigation for stroke for F11 and PROC. A polygenic score integrating cross-ancestry and ancestry-specific stroke GWASs with vascular-risk factor GWASs (integrative polygenic scores) strongly predicted ischaemic stroke in populations of European, East Asian and African ancestry(5). Stroke genetic risk scores were predictive of ischaemic stroke independent of clinical risk factors in 52,600 clinical-trial participants with cardiometabolic disease. Our results provide insights to inform biology, reveal potential drug targets and derive genetic risk prediction tools across ancestries.</p
Stroke genetics informs drug discovery and risk prediction across ancestries
Previous genome-wide association studies (GWASs) of stroke â the second leading cause of death worldwide â were conducted predominantly in populations of European ancestry1,2. Here, in cross-ancestry GWAS meta-analyses of 110,182 patients who have had a stroke (five ancestries, 33% non-European) and 1,503,898 control individuals, we identify association signals for stroke and its subtypes at 89 (61 new) independent loci: 60 in primary inverse-variance-weighted analyses and 29 in secondary meta-regression and multitrait analyses. On the basis of internal cross-ancestry validation and an independent follow-up in 89,084 additional cases of stroke (30% non-European) and 1,013,843 control individuals, 87% of the primary stroke risk loci and 60% of the secondary stroke risk loci were replicated (Pâ<â0.05). Effect sizes were highly correlated across ancestries. Cross-ancestry fine-mapping, in silico mutagenesis analysis3, and transcriptome-wide and proteome-wide association analyses revealed putative causal genes (such as SH3PXD2A and FURIN) and variants (such as at GRK5 and NOS3). Using a three-pronged approach4, we provide genetic evidence for putative drug effects, highlighting F11, KLKB1, PROC, GP1BA, LAMC2 and VCAM1 as possible targets, with drugs already under investigation for stroke for F11 and PROC. A polygenic score integrating cross-ancestry and ancestry-specific stroke GWASs with vascular-risk factor GWASs (integrative polygenic scores) strongly predicted ischaemic stroke in populations of European, East Asian and African ancestry5. Stroke genetic risk scores were predictive of ischaemic stroke independent of clinical risk factors in 52,600 clinical-trial participants with cardiometabolic disease. Our results provide insights to inform biology, reveal potential drug targets and derive genetic risk prediction tools across ancestries
Recommended from our members
A copy of the Senate Congressional Record from April 7, 1970, regarding remarks made by Senator Mike Gravel.
A copy of the Senate Congressional Record from April 7, 1970, regarding remarks made by Senator Mike Gravel
Recommended from our members
A letter from Mike Gravel, Senator from Texas, to Dr. Hector P. Garcia, regarding a rejected nomination of Harrold Carswell.
A letter from Mike Gravel, Senator from Texas, to Dr. Hector P. Garcia, regarding a rejected nomination of Harrold Carswell
Recommended from our members
A copy of the Congressional Record from March 19, 1970 regarding remarks made by Senator Mike Gravel.
A copy of the Congressional Record from March 19, 1970 regarding remarks made by Senator Mike Gravel
The Panama Canal, a reexamination [microform] : a report /
"Serial no. 95-6."Reuse of record except for individual research requires license from LexisNexis Academic & Library Solutions.Issued July 1977.At head of title: 95th Congress, 1st session. Committee print.CIS Microfiche Accession Numbers: CIS 77 S322-6Includes bibliographical references.Microfiche.Mode of access: Internet.condition reviewedcommitted to retai