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- W2989323211 abstract "Neurodegenerative Disease ManagementVol. 9, No. 6 CommentaryFree AccessThe place for electroconvulsive therapy in the management of behavioral and psychological symptoms of dementiaRajesh R Tampi, Deena J Tampi, Juan Young, Rakin Hoq & Kyle ResnickRajesh R Tampi *Author for correspondence: Tel.: +1 203 809 5223; Fax: +1 330 344 2943; E-mail Address: rajesh.tampi@gmail.comhttps://orcid.org/0000-0001-6754-6567Department of Psychiatry & Behavioral Sciences, Cleveland Clinic Akron General, Akron, OH 44307, USACleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH 44195, USASearch for more papers by this author, Deena J TampiDiamond Healthcare, Richmond, VA 23219, USASearch for more papers by this author, Juan YoungDepartment of Psychiatry, Yale School of Medicine, New Haven, CT 06510, USASearch for more papers by this author, Rakin HoqSumma Health Systems/NEOMED Psychiatry Residency Program, Akron, OH 44304, USASearch for more papers by this author & Kyle ResnickSumma Health Systems/NEOMED Psychiatry Residency Program, Akron, OH 44304, USASearch for more papers by this authorPublished Online:8 Nov 2019https://doi.org/10.2217/nmt-2019-0018AboutSectionsPDF/EPUB ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareShare onFacebookTwitterLinkedInReddit Keywords: behavioral and psychological symptoms of dementia (BPSD)disruptive vocalizationelectroconvulsive therapy (ECT)neuropsychiatric symptomsphysical aggressionpostictal confusionThe term ‘behavioral and psychological symptoms of dementia’ (BPSD) is used to describe a group of non-cognitive symptoms and behaviors that are commonly seen among individuals with dementia. BPSD occurs among a third to three-quarters of individuals with dementia, with greater prevalence seen among individuals living in institutional settings [1]. In addition to causing significant emotional distress to the individuals with dementia and their caregivers, BPSD is also associated with significant negative effects including a decline in cognition and function among individuals with dementia, lower the quality of life for individuals with dementia and their caregivers, greater rates of institutionalization for individuals with dementia and greater financial burden to the families of individuals with dementia and the society in general [1].Available evidence indicates that both non-pharmacological and pharmacological interventions are beneficial for the management of BPSD [2]. Pharmacotherapy is usually reserved for those symptoms or behaviors that are refractory to non-pharmacological interventions. In addition, pharmacotherapy is typically used in combination with non-pharmacological interventions for the management of BPSD. Caregiver and staff education along with cognitive stimulation appears to have sustained benefits in the management of BPSD [3]. Current evidence indicates efficacy for antidepressants, anticonvulsants, antipsychotics and cholinesterase inhibitors for the management of BPSD. However, the use of psychotropic medications, especially antipsychotics, for management of BPSD has come under scrutiny due to their significant adverse effects, including cerebrovascular adverse events and death [4].Electroconvulsive therapy (ECT) is an important treatment tool among older adults with psychiatric disorders [5–7]. Evidence indicates efficacy for ECT in the treatment of depression, mania, psychosis and catatonia. It is has been found to be highly effective in emergency situations like malignant catatonia, depression with psychotic or catatonic features and among individuals with threatening suicidal behaviors. ECT also appears to have greater benefit among older adults when compared with younger adults [6]. In addition, ECT appears to be a safe treatment among older adults with few contraindications and transient or limited number of adverse effects.Over the past two decades, there has been growing interest in using ECT among individuals with BPSD [8]. In this article, we review the evidence for using ECT in the management of BPSD. Based on the available evidence, we make recommendations on when the use of ECT is appropriate among individuals with BPSD. We searched the databases PubMed and Ovid Medline using two keywords: ‘ECT’ and ‘dementia’. In addition, we also reviewed the references of included studies for additional papers. We only included published studies that evaluated the use of ECT for BPSD in this report, irrespective of the type of study.Evidence for using ECT in the management of BPSDA review of the literature indicates that there are 20 published reports on the use of ECT for the management of BPSD [9–28]. These reports included a total of 172 individuals with dementia. A majority of these studies were case reports (eight of 20, 40%) followed by retrospective chart reviews (five, 25%) and case series (four, 20%). There was only one prospective cohort study [23], one case–control study [24] and one prospective observational study [27]. A majority of the individuals had Alzheimer's disease (68 of 172, 40%) followed by unspecified dementia (25, 15%) and vascular dementia (22, 13%). Bitemporal followed by right unilateral and bilateral were the most common electrode placements. Twelve of the studies (60%) were reported from the US followed by four from Canada and one each from The Netherlands, Germany, Italy and China. It appears that over 90% of the individuals who were treated with ECT responded to treatment with a resolution of target symptoms including verbal and physical aggression and suicidal behaviors. Adverse effects from the ECT were infrequent and when they did occur, were mild and transient. The most common adverse event that was reported was postictal confusion/memory impairment in approximately 25 (15%) of the individuals. Table 1 provides details of these published papers obtained via a literature search.Table 1. Summary of published studies on the use of electroconvulsive therapy for the management of behavioral and psychological symptoms of dementia.Study (year)CountryType of studyNumber of patientsType of patientsType of ECTTarget behaviorsOutcomesAdverse effectsRef.Carlyle et al. (1991)CanadaCase series3Dementia, type not specifiedBilateralVerbal aggression (disruptive vocalizations)Improvement in symptomsNone reported[9]Holmberg et al. (1996)USACase report1Dementia, type not specifiedBilateralVerbal and physical aggressionImprovement in symptomsNone reported[10]Roccaforte et al. (2000)USACase report1Dementia, type not specifiedNot statedVerbal aggression (disruptive vocalizations)Improvement in symptomsNone reported[11]Grant et al. (2001)USACase series4ADBilateral3 – verbal and physical aggression 1 – verbal aggressionImprovement in symptomsNone reported[12]Reid (2006)USACase report1Pick's diseaseNot statedVerbal and physical aggressionNo benefitNone stated[13]Sutor et al. (2008)USARetrospective chart review11AD8 – bitemporal 2 – right unilateral 1 – bifrontalVerbal and physical aggressionNine of 11 showed improvement in symptoms7 – no adverse effects noted 2 – decreased cognition 1 – somnolence and atrial fibrillation requiring cardioversion 1 – urinary retention[14]Bang et al. (2008)USACase reports21 – AD and Parkinson's disease 1 – congenital hydrocephalusBilateralVerbal aggression (disruptive vocalizations)Improvement in symptomsNone noted[15]Wu et al. (2010)USACase reports21 – AD 1 – FTDBitemporalPhysical aggressionImprovement in symptomsNone noted[16]Ujkaj et al. (2012)USARetrospective chart review168 – AD 3 – VD 2 – FTD 3 – unspecified dementia12 – bilateral 4 – right unilateralVerbal and physical aggression15 of the 16 patients showed improvement in symptoms8 – transient postictal confusion 2 – more severe postictal confusion No other serious adverse effects noted[17]Kramer et al. (2013)The NetherlandsCase series3ADBilateralVerbal and physical aggressionImprovement in target behaviorsNo serious adverse effects noted[18]Aksay et al. (2014)GermanyCase report1ADRight unilateralVerbal and physical aggressionImprovement in target behaviorsNo serious adverse effects noted, headaches after first three sessions[19]Tang et al. (2014)USARetrospective chart review42Dementia, type not specifiedRight unilateral and bifrontalAgitationNot noted in the abstractNot noted in the abstract[20] (Abstract only)Dare et al. (2015)USACase series1ADBilateral and right unilateralBehavioral dyscontrolImprovement in target behaviorsNone noted[21]Fàzzari et al. (2015)ItalyCase report1ADBifrontal and bitemporalRestlessness, mood liability and verbal aggressionImprovement in target behaviorsNone noted[22]Acharya et al. (2015)USAProspective cohort study2313 – AD 4 – VD 1 – FTD 2 – mixed dementia 3 – unspecified dementiaRight unilateral and bifrontalAgitation or aggression21 out of the 23 participants responded to treatment with improvement in symptoms21 out of the 23 participants tolerated the treatments well, two participants developed post ECT delirium, one participant developed atrial fibrillation but continued to receive ECT[23]Zhang et al. (2016)ChinaCase–control study238 – AD 8 – VD 4 – FTD 3 – unspecified dementiaBitemporal16 – high risk for suicide 6 – high risk for aggression 1 – insufficient response to pharmacotherapy or intolerable adverse effects21 out of the 23 participants responded to treatment with improvement in symptoms7 – transient memory impairment 1 – headache 1 – myalgia 1 – mild dyspnea 1 – transient hypertension[24]Isserles et al. (2017)CanadaRetrospective chart review2511 – AD 5 – VD 4 – LBD 3 – FTD 9 – unspecified dementia 3 – mixed (A + VD)Bitemporal Right unilateral to bitemporal-3 Bitemporal to right unilateral-1Severe and resistant BPSD72% – marked response for acute treatment course 87% – marked response for maintenance courseClinical note 7% – significant cognitive adverse effects in acute course 13% – significant cognitive adverse effects in the maintenance course Attending psychiatrist score 21% – significant cognitive adverse effects[25]Lau et al. (2017)CanadaRetrospective chart review53 – AD 2 – mixed dementia (AD + VD)BitemporalVerbal aggression (disruptive vocalizations)Improvement in target behaviors (p < 0.0001)1 – transient post ECT delirium[26]Burton et al. (2017)USAProspective observational study63 – AD 2 – VD 1 – unspecified dementiaBitemporalSevere behavioral disturbancesImprovement in target behaviors0 – adverse events necessitating ECT discontinuation. 1 – post-ECT nausea, remitted with intravenous ondansetron 1 – post-emergence agitation, resolved with intravenous diazepam[27]Selvadurai et al. (2018)CanadaCase report1Frontolobar degenerationBitemporalPhysical aggression and inappropriate sexual behaviorsImprovement in target behaviorsNone reported[28]AD: Alzheimer's disease; BPSD: Behavioral and psychological symptoms of dementia; ECT: Electroconvulsive therapy; FTD: Frontotemporal dementia; LBD: Lewy body dementia; VD: Vascular dementia.Although the therapeutic mechanism of ECT is unclear, it is postulated that ECT benefit individuals with BPSD by enhancing the transmission of neurochemicals including GABA, glutamate, dopamine and norepinephrine in the brain [29–33].Two recent systematic reviews have evaluated the literature on the use of ECT for the management of BPSD. In the first review, Glass et al. found 11 papers that included a total of 216 individuals with BPSD who were treated with ECT [34]. The authors reported that despite being limited to case reports, case series, retrospective chart review, retrospective case–control and an open-label prospective study, ECT demonstrated promise in reducing agitation among individuals with dementia. Additionally, in those individuals who had a relapse in symptoms, they found benefit from maintenance ECT. In the second systematic review by van den Berg et al., the authors found 17 reports that evaluated the use of ECT among individuals with BPSD [35]. The investigators reported that they found one prospective cohort study and one case–control study, whereas the others were retrospective chart reviews, case series or case reports. They reported that clinically significant improvement was observed in 88% of the 122 individuals in these studies and the effect was often noted early in the treatment course. Additionally, the adverse effects were most often mild, transient or not reported.Two recent reports also indicate that ECT does not increase the risk of dementia [36,37]. Additionally, there is no evidence that ECT worsens cognition among individuals with dementia [38–40].The findings of this report are similar to the two above-mentioned systematic reviews. There is emerging evidence that ECT appears to be beneficial in treating individuals with BPSD and is fairly well tolerated. However, the major limitations of available data are as mentioned in the two systematic reviews – there is substantial risk of selection bias in these studies, the study designs are not randomized controlled trials, and there are a limited number of studies with few participants available in the literature.Place for using ECT in the management of BPSDBased on the available evidence from a search of the literature, it is our opinion that ECT appears to be a viable treatment option for individuals with BPSD. It appears to be particularly suited for use among individuals who have had an inadequate response to non-pharmacological and pharmacological treatment strategies, among those individuals who have tolerability issues to pharmacotherapy, and also among those individuals in whom there is a need for the quick resolution of symptoms for their safety and well being.We agree with Burgut et al. who caution that the decision to use ECT among individuals with BPSD should be done after a thoughtful review of all available treatment options [8]. The authors remind us that the use of ECT among individuals with BPSD would be an ‘off-label’ indication. They further caution us that ECT remains a controversial treatment in medicine, not due to any clinical or scientific evidence regarding its efficacy and safety, but due to societal misperception about its use among patients with mental health disorders. The authors recommend the use of ECT among individuals with BPSD only when all other treatment options have failed, and with the informed consent of the individual with dementia or their surrogate decision makers who are fully appraised of the potential risks of the treatment. The authors also recommend ongoing risk–benefit analysis of the treatment trial to maximize gains and reduce harm from the ECT treatments.Conclusion & future perspectiveAs the available evidence for the use of non-pharmacological treatment modalities for the management of BPSD is strong, additional well-controlled and larger trials on the use of such treatments are expected in the near future. Given the strength of existing evidence, regulatory authorities will require that non-pharmacological treatment modalities must be tried among individuals with BPSD, before embarking on pharmacotherapeutic trials given the concern over adverse-effect profiles of these medications. There is growing literature on the use of ECT for the management of BPSD. Available evidence indicates that ECT is effective and well tolerate among individuals with BPSD. However, the evidence is limited to uncontrolled trails and to a limited number of individuals. As there is significant concern for the use of pharmacotherapeutic agents among individuals with BPSD, and the evidence for the use of ECT among individuals with BPSD is growing, well controlled and larger trials of the use of ECT for the management of BPSD can be anticipated in the near future. If the evidence from these new trials is robust and confirms the findings that ECT is well tolerated and beneficial to individuals with BPSD, ECT will have a definitive place among management strategies for BPSD. However, given the public perception of ECT, it is difficult to envisage the use of ECT among individuals with BPSD except in refractory cases or in cases where the response to other treatments is slow or limited by tolerability issues.Financial & competing interests disclosureThe authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.No writing assistance was utilized in the production of this manuscript.References1. Tampi RR, Williamson D, Muralee S et al. Behavioral and psychological symptoms of dementia: part I-epidemiology, neurobiology, heritability, and evaluation. Clin. Geriatrics 19, 41–46 (2011).Google Scholar2. Tampi RR, Williamson D, Muralee S et al. Behavioral and psychological symptoms of dementia: part II treatment. Clin. Geriatrics 19, 31–40 (2011).Google Scholar3. Livingston G, Johnston K, Katona C et al. Systematic review of psychological approaches to the management of neuropsychiatric symptoms of dementia. Am. J. Psych. 162, 1996–2021 (2005).Crossref, Medline, Google Scholar4. Mittal V, Kurup L, Williamson D, Muralee S, Tampi RR. Risk of cerebrovascular adverse events and death in elderly patients with dementia when treated with antipsychotic medications: a literature review of evidence. Am. J. Alz. Dis. Other Demen. 26, 10–28 (2011).Crossref, Medline, Google Scholar5. van der Wurff FB, Stek ML, Hoogendijk WJ, Beekman AT. The efficacy and safety of ECT in depressed older adults: a literature review. Int. J. Geriatr. Psych. 18(10), 894–904 (2003).Crossref, Medline, Google Scholar6. Meyer JP, Swetter SK, Kellner CH. Electroconvulsive therapy in geriatric psychiatry: a selective review. Psychiatr. Clin. North Am. 41(1), 79–93 (2018).Crossref, Medline, Google Scholar7. McDonald WM. Neuromodulation treatments for geriatric mood and cognitive disorders. Am. J. Geriatr. Psych. 24(12), 1130–1141 (2016).Crossref, Medline, Google Scholar8. Burgut FT, Popeo D, Kellner CH. ECT for agitation in dementia: is it appropriate? Med. Hypotheses 75(1), 5–6 (2010).Crossref, Medline, Google Scholar9. Carlyle W, Killick L, Ancill R. ECT: an effective treatment in the screaming demented patient. J. Am. Geriatr. Soc. 39(6), 637 (1991).Crossref, Medline, CAS, Google Scholar10. Holmberg SK, Tariot PN, Challapalli R. Efficacy of ECT for agitation in dementia: a case report. Am. J. Geriatr. Psych. 4(4), 330–334 (1996).Medline, Google Scholar11. Roccaforte WH, Wengel SP, Burke WJ. ECT for screaming in dementia. Am. J. Geriatr. Psych. 8(2), 177 (2000).Crossref, Medline, CAS, Google Scholar12. Grant JE, Mohan SN. Treatment of agitation and aggression in four demented patients using ECT. J. ECT 17(3), 205–209 (2001).Crossref, Medline, CAS, Google Scholar13. Reid C. Medicating “Margaret”. J. Clin. Ethics 17(4), 340–343 (2006).Medline, Google Scholar14. Sutor B, Rasmussen KG. Electroconvulsive therapy for agitation in Alzheimer disease: a case series. J. ECT 24(3), 239–241 (2008).Crossref, Medline, Google Scholar15. Bang J, Price D, Prentice G, Campbell J. ECT treatment for two cases of dementia-related pathological yelling. J. Neuropsych. Clin. Neurosci. 20(3), 379–380 (2008).Crossref, Medline, Google Scholar16. Wu Q, Prentice G, Campbell JJ. ECT treatment for two cases of dementia-related aggressive behavior. J. Neuropsych. Clin. Neurosci. 22(2), E10–E11 (2010).Crossref, Medline, CAS, Google Scholar17. Ujkaj M, Davidoff DA, Seiner SJ, Ellison JM, Harper DG, Forester BP. Safety and efficacy of electroconvulsive therapy for the treatment of agitation and aggression in patients with dementia. Am. J. Geriatr. Psych. 20(1), 61–72 (2012).Crossref, Medline, Google Scholar18. Kramer BL, Albronda T, Clarenbach-Wierda DL. Electro-convulsive treatment of elderly patients with both behavioral problems and dementia. Tijdschr. Psychiatr. 55(12), 949–953 (2013).Medline, CAS, Google Scholar19. Aksay SS, Hausner L, Frölich L, Sartorius A. Severe agitation in severe early-onset Alzheimer's disease resolves with ECT neuropsychiatr. Dis. Treat. 10, 2147–2151 (2014).Medline, Google Scholar20. Tang Y, Herminda A, Khanh H, Laddha SR, McDonald WM. Efficacy and safety of ECT for behavioral and psychological symptoms of dementia (BPSD): a retrospective chart review. Am. J. Geriatr. Psych. 22(3), S114–S115 (2014).Crossref, Google Scholar21. Dare FY, Rasmussen KG. Court-approved electroconvulsive therapy in patients unable to provide their own consent: a case series. J. ECT 31(3), 147–149 (2015).Crossref, Medline, Google Scholar22. Fàzzari G, Marangoni C, Benzoni O, Maintenance ECT. for the treatment and resolution of agitation in Alzheimer's dementia. J. Psychopathol. 21, 159–160 (2015).Google Scholar23. Acharya D, Harper DG, Achtyes ED et al. Safety and utility of acute electroconvulsive therapy for agitation and aggression in dementia. Int. J. Geriatr. Psych. 30(3), 265–273 (2015).Crossref, Medline, Google Scholar24. Zhang QE, Sha S, Ungvari GS et al. Demographic and clinical profile of patients with dementia receiving electroconvulsive therapy: a case–control study. J. ECT 32(3), 183–186 (2016).Crossref, Medline, Google Scholar25. Isserles M, Daskalakis ZJ, Kumar S, Rajji TK, Blumberger DM. Clinical effectiveness and tolerability of electroconvulsive therapy in patients with neuropsychiatric symptoms of dementia. J. Alzheimers Dis. 57(1), 45–51 (2017).Crossref, Medline, Google Scholar26. Lau TE, Babani PK, McMurray LA. The treatment of disruptive vocalization in dementia (behavioral and psychological symptoms of dementia) with electroconvulsive therapy: a case series. J. ECT 33(2), e9–e13 (2017).Crossref, Medline, Google Scholar27. Burton MC, Koeller SL, Brekke FM, Afonya AT, Sutor B, Lapid MI. Use of electroconvulsive therapy in dementia-related agitation: a case series. J. ECT 33(4), 286–289 (2017).Crossref, Medline, Google Scholar28. Selvadurai MI, Waxman R, Ghaffar O, Fischler I. Efficacy and safety of maintenance electroconvulsive therapy for sustaining resolution of severe aggression in a major neurocognitive disorder. BMJ Case Rep. 2018, doi:10.1136/bcr-2017-222100 (2018).Medline, Google Scholar29. McIlroy S, Craig D. Neurobiology and genetics of behavioural syndromes of Alzheimer's disease. Curr. Alzheimer Res. 1(2), 135–142 (2004).Crossref, Medline, CAS, Google Scholar30. Tascone LDS, Bottino CMC. Neurobiology of neuropsychiatric symptoms in Alzheimer's disease: a critical review with a focus on neuroimaging. Dement. Neuropsychol. 7(3), 236–243 (2013).Crossref, Medline, Google Scholar31. Devanand DP, Shapira B, Petty F et al. Effects of electroconvulsive therapy on plasma GABA. Convuls. Ther. 11(1), 3–13 (1995).Medline, CAS, Google Scholar32. Mann JJ. Neurobiological correlates of the antidepressant action of electroconvulsive therapy. J. ECT 14(3), 172–180 (1998).Crossref, Medline, CAS, Google Scholar33. Newman ME, Gur E, Shapira B, Lerer B. Neurochemical mechanisms of action of ECS: evidence from in vivo studies. J. ECT 14(3), 153–171 (1998).Crossref, Medline, CAS, Google Scholar34. Glass OM, Forester BP, Hermida AP. Electroconvulsive therapy (ECT) for treating agitation in dementia (major neurocognitive disorder) – a promising option. Int. Psychogeriatr. 29(5), 717–726 (2017).Crossref, Medline, Google Scholar35. van den Berg JF, Kruithof HC, Kok RM, Verwijk E, Spaans HP. Electroconvulsive therapy for agitation and aggression in dementia: a systematic review. Am. J. Geriatr. Psych. 26(4), 419–434 (2018).Crossref, Medline, Google Scholar36. Osler M, Rozing MP, Christensen GT, Andersen PK, Jørgensen MB. Electroconvulsive therapy and risk of dementia in patients with affective disorders: a cohort study. Lancet Psych. 5(4), 348–356 (2018).Crossref, Medline, Google Scholar37. Chu CW, Chien WC, Chung CH et al. Electroconvulsive therapy and risk of dementia – a nationwide cohort study in Taiwan. Front. Psych. 9, 397 (2018).Crossref, Medline, Google Scholar38. Rao V, Lyketsos CG. The benefits and risks of ECT for patients with primary dementia who also suffer from depression. Int. J. Geriatr. Psych. 15(8), 729–735 (2000).Crossref, Medline, CAS, Google Scholar39. Oudman E. Is electroconvulsive therapy (ECT) effective and safe for treatment of depression in dementia? A short review. J. ECT 28(1), 34–38 (2012).Crossref, Medline, Google Scholar40. Hausner L, Damian M, Sartorius A, Frölich L. Efficacy and cognitive side effects of electroconvulsive therapy (ECT) in depressed elderly inpatients with coexisting mild cognitive impairment or dementia. J. Clin. Psych. 72(1), 91–97 (2011).Crossref, Google ScholarFiguresReferencesRelatedDetailsCited ByManaging Behavioral and Psychological Symptoms of Dementia (BPSD) in the Era of Boxed Warnings4 July 2022 | Current Psychiatry Reports, Vol. 24, No. 9Prescribing in Older People17 December 2021Update on Pharmacological Treatment of Neuropsychiatric Symptoms of Dementia31 March 2021 | Current Geriatrics Reports, Vol. 10, No. 2Agitation and Dementia: Prevention and Treatment Strategies in Acute and Chronic Conditions16 April 2021 | Frontiers in Neurology, Vol. 12 Vol. 9, No. 6 Follow us on social media for the latest updates Metrics History Received 26 August 2019 Accepted 4 October 2019 Published online 8 November 2019 Published in print December 2019 Information© 2019 Future Medicine LtdKeywordsbehavioral and psychological symptoms of dementia (BPSD)disruptive vocalizationelectroconvulsive therapy (ECT)neuropsychiatric symptomsphysical aggressionpostictal confusionFinancial & competing interests disclosureThe authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.No writing assistance was utilized in the production of this manuscript.PDF download" @default.
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- W2989323211 cites W1969891661 @default.
- W2989323211 cites W1978812597 @default.
- W2989323211 cites W1982170004 @default.
- W2989323211 cites W1989191595 @default.
- W2989323211 cites W1995681270 @default.
- W2989323211 cites W2014179747 @default.
- W2989323211 cites W2052277182 @default.
- W2989323211 cites W2052716093 @default.
- W2989323211 cites W2059782974 @default.
- W2989323211 cites W2064011829 @default.
- W2989323211 cites W2066597977 @default.
- W2989323211 cites W2073056559 @default.
- W2989323211 cites W2077958806 @default.
- W2989323211 cites W2099740162 @default.
- W2989323211 cites W2150798548 @default.
- W2989323211 cites W2314956286 @default.
- W2989323211 cites W2334899133 @default.
- W2989323211 cites W2521805263 @default.
- W2989323211 cites W2561201103 @default.
- W2989323211 cites W2573633705 @default.
- W2989323211 cites W2586900212 @default.
- W2989323211 cites W2726685410 @default.
- W2989323211 cites W2758691497 @default.
- W2989323211 cites W2773189073 @default.
- W2989323211 cites W2792133158 @default.
- W2989323211 cites W2890209539 @default.
- W2989323211 cites W4231874723 @default.
- W2989323211 cites W4242451416 @default.
- W2989323211 cites W4298436338 @default.
- W2989323211 cites W4312449770 @default.
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