“…Epilepsy significantly reduces the quality of life for patients, family members, and caregivers. Several studies have documented the increased direct cost (including diagnosis, management, and treatment) of epilepsy using quality‐of‐life or model estimates, evaluation of the effect of pharmacologic treatment or management issues related to the care of patients with epilepsy, including the effect on caregivers and families, as well as the influence on economic and other costs (Begley & Beghi, 2002; Begley et al., 2002; Leonardi & Ustun, 2002; Argumosa & Herranz, 2004; Ekman & Forsgren, 2004; Beghi et al., 2005; Forsgren et al., 2005; Wilby et al., 2005; Garcia‐Contreras et al., 2006; Whiting et al., 2006; Camfield & Camfield, 2007; Duh et al., 2007; Jacoby & Austin, 2007; Komarek & Smidova, 2007; Langfitt et al., 2007; Mistry et al., 2007; Pugliatti et al., 2007; Wilson et al., 2007; De Boer et al., 2008; Jette et al., 2008; Strzelczyk et al., 2008; Vera‐Llonch et al., 2008; Beghi et al., 2009; Pena et al., 2009; van Andel et al., 2009). Using an average of different studies the range for the mean annual direct costs has been estimated to be $4,748 (adjusted to 2006 values) in a German epilepsy center.…”