ADHD Pharmacotherapy and Mortality in Individuals With ADHD

Author:

Li Lin1,Zhu Nanbo1,Zhang Le1,Kuja-Halkola Ralf1,D’Onofrio Brian M.12,Brikell Isabell13,Lichtenstein Paul1,Cortese Samuele4567,Larsson Henrik8,Chang Zheng1

Affiliation:

1. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden

2. Department of Psychological and Brain Sciences, Indiana University, Bloomington

3. Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway

4. Centre for Innovation in Mental Health–School of Psychology, Faculty of Environmental and Life Sciences, and Clinical and Experimental Sciences (CNS and Psychiatry), Faculty of Medicine, University of Southampton, Southampton, United Kingdom

5. New York University Child Study Center, Hassenfeld Children’s Hospital at NYU Langone, New York

6. Solent NHS Trust, Southampton, United Kingdom

7. Department of Precision and Regenerative Medicine and Ionian Area (DIMEPRE-J), University of Studies of Bari Aldo Moro, Bari, Italy

8. School of medical sciences, Örebro University, Örebro, Sweden

Abstract

ImportanceAttention-deficit/hyperactivity disorder (ADHD) is associated with increased risks of adverse health outcomes including premature death, but it is unclear whether ADHD pharmacotherapy influences the mortality risk.ObjectiveTo investigate whether initiation of ADHD pharmacotherapy was associated with reduced mortality risk in individuals with ADHD.Design, Setting, and ParticipantsIn an observational nationwide cohort study in Sweden applying the target trial emulation framework, we identified individuals aged 6 through 64 years with an incident diagnosis of ADHD from 2007 through 2018 and no ADHD medication dispensation prior to diagnosis. Follow-up started from ADHD diagnosis until death, emigration, 2 years after ADHD diagnosis, or December 31, 2020, whichever came first.ExposuresADHD medication initiation was defined as dispensing of medication within 3 months of diagnosis.Main Outcomes and MeasuresWe assessed all-cause mortality within 2 years of ADHD diagnosis, as well as natural-cause (eg, physical conditions) and unnatural-cause mortality (eg, unintentional injuries, suicide, and accidental poisonings).ResultsOf 148 578 individuals with ADHD (61 356 females [41.3%]), 84 204 (56.7%) initiated ADHD medication. The median age at diagnosis was 17.4 years (IQR, 11.6-29.1 years). The 2-year mortality risk was lower in the initiation treatment strategy group (39.1 per 10 000 individuals) than in the noninitiation treatment strategy group (48.1 per 10 000 individuals), with a risk difference of −8.9 per 10 000 individuals (95% CI, −17.3 to −0.6). ADHD medication initiation was associated with significantly lower rate of all-cause mortality (hazard ratio [HR], 0.79; 95% CI, 0.70 to 0.88) and unnatural-cause mortality (2-year mortality risk, 25.9 per 10 000 individuals vs 33.3 per 10 000 individuals; risk difference, −7.4 per 10 000 individuals; 95% CI, −14.2 to −0.5; HR, 0.75; 95% CI, 0.66 to 0.86), but not natural-cause mortality (2-year mortality risk, 13.1 per 10 000 individuals vs 14.7 per 10 000 individuals; risk difference, −1.6 per 10 000 individuals; 95% CI, −6.4 to 3.2; HR, 0.86; 95% CI, 0.71 to 1.05).Conclusions and RelevanceAmong individuals diagnosed with ADHD, medication initiation was associated with significantly lower all-cause mortality, particularly for death due to unnatural causes.

Publisher

American Medical Association (AMA)

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