neurology news from the inaugural european ispor meeting

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6 I_n_t_e_r_n_a_t1_' o__ n_a_l __ R_e_s_e_a __ rc__ h_a_n_d __O ..... p_i_n_i.o_n s _ 1I Neurology news from the inaugural European ISPOR meeting [Cologne, Gennany December 1998] which increased 4-fold from mild to severe disease. Total mean costs over the 3-month period were £6 616 per patient with moderate Alzheimer's and £13593 per patient with severe Alzheimer's [see table]. :Cost of Alzheimer's disease in UK i according to disease severity ITotal direct medical costs 199 902 3387 Severe 636 3165 Disease severity Moderate 474 Mild 1220 188 Contro" ICost i Total direct non-medical costs I ! At the first annual meeting of the International Society for Pharmacoeconomics and Outcomes Research (ISPOR), Dr Joel Hay from the University of Southern California College of Pharmacy, Los Angeles, US, commented on the exponential growth in pharmacoeconomics since its birth around 20 years ago. Describing pharmacoeconomics as a young discipline suffering from growing pains, he commented that today there is a desire for methodological standards and consistency in pharmacoeconomic evaluation. A selection of pharmacoeconomic evaluations presented at the conference that had a neurological focus are outlined below. Pramipexole favourable in Canada, Gennanyand Sweden Pramipexole was cost effective for the treatment of early and advanced Parkinson's disease, in a modelling study conducted from the perspective of Canada, Germany and Sweden. However, results were subject to the limitations of modelling chronic disease progression and subsequent health utility and costs. A cost-effectiveness model was developed that linked Unified Parkinson's Disease Rating Scale (UPDRS) Part II (ADL) and Part III (Motor) scores to The researchers suggested that this was a result of the increased need for more intensive, medical care in patients with severe disease. Pramipexole vs bromocriptine in Parkinson's disease Patients with Parkinson's disease treated with prarnipexole or bromocriptine scored significantly better than placebo recipients in some aspects of the Functional Status Questionnaire (FSQ), according to the results of a multicentre trial conducted in 7 countries. The study also showed that EuroQOL visual analog scale (VAS) scores were significantly better for prarnipexole recipients than for placebo recipients. The FSQ and EuroQOL VAS were used to measure functional and health status, respectively, in 247 patients (aged 30 years) with advanced idiopathic Parkinson's disease. Patients received either prarnipexole 4.5 mg/ day (n = 80), bromocriptine 30 mg/day (84) or placebo (83). Approximately 9 months after initiating therapy, scores for the FSQ domains of mental health and basic activities of daily living were significantly better for pramipexole and bromocriptine recipients than for placebo recipients. Patients treated with prarnipexole also scored significantly better than placebo recipients for the FSQ domains intermediate activities of daily living (ADL) and days cut down on usual activities. Scores for the FSQ and EuroQOL instruments varied with disease severity. Getting ahead of headache German researchers have developed a disease management programme that improves the quality of headache treatment. However, the researchers say that the burden of headache and migraine could be further reduced with more collaborative efforts by physicians and pharmacists. 341 employees from a company with a sickness fund who suffered from headache responded to the Short Form-36, the Kiel Headache Questionnaire and additional questions about medication and satisfaction with therapy. The respondents, their physicians and pharmacists were given information on management and prevention of headache. Respondents were then given a second follow-up questionnaire about the impact of the programme. 126 of 183 traceable initial respondents answered the second questionnaire. 29.1% of sufferers reported an improvement in health status, 43.1 % reported less headaches, 38.9% reported shorter headache attacks, 22.6% had improvement in identifying trigger factors, 21 % used less medication and 41.9% learned a relaxation technique. Work time lost due to sickness was also reduced. Cost of Alzheimer's substantial in UK The cost of care of Alzheimer's disease is substantial in the UK, and is directly related to severity of disease, indicate the results of a multicentre study retrospectively conducted in that country. Direct medical costs, direct non-medical costs and indirect costs were calculated for 128 patients with mild (n = 38), moderate (42) and severe (48) Alzheimer's disease and 56 controls over 3 months' treatment (1993 pounds sterling). Indirect costs were the main cost driver for patients (63-74% of a total cost of £30459) and were mainly due to time spent by the caregiver with the patient. Direct costs represented 18-31 % of the total cost and were mainly due to institutionalisation or hospitalisation. Direct non-medical costs accounted for 6-7% of the total cost. All costs increased with disease severity, particularly costs for hospitalisation and institutionalisation, !Total indirect costs NA 4923 6449 9304 PharmacoEconomics & Outcomes News 9 Jan 1998 No. 194 1173-5503199/0194-0006/$01.00° Adlslnternational Limited 1999. All rights reserved

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6 I_n_t_e_r_n_a_t1_'o__n_a_l__R_e_s_e_a__rc__h_a_n_d__O.....p_i_n_i.o_ns_

1I

Neurology news from the inaugural European ISPOR meeting[Cologne, Gennany December 1998]

which increased 4-fold from mild to severe disease.Total mean costs over the 3-month period were £6 616per patient with moderate Alzheimer's and £13593per patient with severe Alzheimer's [see table].

:Cost of Alzheimer's disease in UKi according to disease severity

ITotal direct medical costs

199

902

3387

Severe

636

3165

Disease severity

Moderate

474

Mild

1220

188

Contro"ICost

iTotal direct non-medical costsI!

At the first annual meeting of the InternationalSociety for Pharmacoeconomics and OutcomesResearch (ISPOR), Dr Joel Hay from the Universityof Southern California College of Pharmacy, LosAngeles, US, commented on the exponential growthin pharmacoeconomics since its birth around 20 yearsago. Describing pharmacoeconomics as a youngdiscipline suffering from growing pains, he commentedthat today there is a desire for methodological standardsand consistency in pharmacoeconomic evaluation.A selection of pharmacoeconomic evaluationspresented at the conference that had a neurologicalfocus are outlined below.

Pramipexole favourable in Canada,Gennanyand Sweden

Pramipexole was cost effective for the treatmentof early and advanced Parkinson's disease, in amodelling study conducted from the perspective ofCanada, Germany and Sweden. However, results weresubject to the limitations of modelling chronic diseaseprogression and subsequent health utility and costs.

A cost-effectiveness model was developed thatlinked Unified Parkinson's Disease Rating Scale(UPDRS) Part II (ADL) and Part III (Motor) scores to

The researchers suggested that this was a resultof the increased need for more intensive, medical carein patients with severe disease.

Pramipexole vs bromocriptinein Parkinson's disease

Patients with Parkinson's disease treated withprarnipexole or bromocriptine scored significantlybetter than placebo recipients in some aspects of theFunctional Status Questionnaire (FSQ), according to theresults of a multicentre trial conducted in 7 countries.The study also showed that EuroQOL visual analogscale (VAS) scores were significantly better forprarnipexole recipients than for placebo recipients.

The FSQ and EuroQOL VAS were used to measurefunctional and health status, respectively, in 247 patients(aged ~ 30 years) with advanced idiopathic Parkinson'sdisease. Patients received either prarnipexole ~ 4.5 mg/day (n = 80), bromocriptine ~ 30 mg/day (84) orplacebo (83).

Approximately 9 months after initiating therapy,scores for the FSQ domains of mental health andbasic activities of daily living were significantly betterfor pramipexole and bromocriptine recipients than forplacebo recipients. Patients treated with prarnipexolealso scored significantly better than placebo recipientsfor the FSQ domains intermediate activities of dailyliving (ADL) and days cut down on usual activities.Scores for the FSQ and EuroQOL instruments variedwith disease severity.

Getting ahead of headacheGerman researchers have developed a disease

management programme that improves the quality ofheadache treatment. However, the researchers say thatthe burden of headache and migraine could be furtherreduced with more collaborative efforts by physiciansand pharmacists.

341 employees from a company with a sicknessfund who suffered from headache responded to theShort Form-36, the Kiel Headache Questionnaire andadditional questions about medication and satisfactionwith therapy. The respondents, their physicians andpharmacists were given information on managementand prevention of headache. Respondents were thengiven a second follow-up questionnaire about theimpact of the programme.

126 of 183 traceable initial respondents answeredthe second questionnaire. 29.1 % of sufferers reportedan improvement in health status, 43.1 % reported lessheadaches, 38.9% reported shorter headache attacks,22.6% had improvement in identifying trigger factors,21 % used less medication and 41.9% learned arelaxation technique. Work time lost due to sicknesswas also reduced.

Cost of Alzheimer's substantial in UKThe cost of care of Alzheimer's disease is substantial

in the UK, and is directly related to severity of disease,indicate the results of a multicentre study retrospectivelyconducted in that country.

Direct medical costs, direct non-medical costs andindirect costs were calculated for 128 patients with mild(n = 38), moderate (42) and severe (48) Alzheimer'sdisease and 56 controls over 3 months' treatment(1993 pounds sterling).

Indirect costs were the main cost driver for patients(63-74% of a total cost of £30459) and were mainlydue to time spent by the caregiver with the patient.Direct costs represented 18-31 % of the total cost andwere mainly due to institutionalisation or hospitalisation.Direct non-medical costs accounted for 6-7% of thetotal cost.

All costs increased with disease severity, particularlycosts for hospitalisation and institutionalisation,

!Total indirect costs

NA 4923 6449 9304

PharmacoEconomics & Outcomes News 9 Jan 1998 No. 194 1173-5503199/0194-0006/$01.00°Adlslnternational Limited 1999. All rights reserved

INTERNATIONAL RESEARCH & OPINION7

disease progression, costs and quality-adjusted lifeyears (QALYs). Data were derived from the medicalliterature, clinical trials and a survey of resource useand health utility for 193 patients.

The incremental cost effectiveness of pramipexole,relative to baseline treatment, was estimated usingcost and QALY estimates from the model. Early andadvanced Parkinson's patients were analysedseparately and sensitivity analyses were performed.

In Sweden, pramipexole treatment had lowercosts and was more effective than baseline treatment.In Germany and Canada, pramipexole treatment hadhigher costs but was more effective than baselinetreatment.

CE ratios relatively lowCost-effectiveness ratios were lower than those

used for many commonly used medical therapies.TI:e incremental cost-effectiveness ratios for patientsWIth early-stage Parkinson's disease in Sweden,Germany and Canada were -SEK41 161, DM26 780and $Can28 097, respectively (1997 values). Ratiosfor patients with advanced-stage Parkinson's diseasewere -SEK27 386, DM49 168 and $Can25 090respectively. Pramipexole is also a favourable o~tionin Parkinson's disease in thc US.*

milSltl!:!

1173.5503199/0194-00071$01.00°Adlalnternatlonal Llmltecl1999. All rlghta reaerved

Cost and mortality of Parkinson's disease

Healthcare costs and mortality in Parkinson'sdisease are significant and emphasise the need forimproved treatment, say researchers in Scotland.

A controlled study was conducted using 2 popu­lations in Tayside, Scotland; a 7-year cohort (1989­1995; n = 30 (00) and an ll-year cohort (1985-1995;10000). Incident cases were identified, and thosewho had taken antipsychotics were excluded, usingthe first 6 months of data. Each case was matchedto 9 controls.

The incidence of Parkinson's disease was 108 and33 in the 7- and II-year cohorts, respectively. Mediancosts of hospitalisation were significantly higher inParkinson's disease compared with controls (£14 119vs £5077, respectively). The relative risk of mortalityin patients with Parkinson's disease was similarbetween the 2 cohorts (2.5 after 7 years and 2.25 afterII years). This risk was significantly greater than thatfor controls.

The researchers said that the robustness of thecosting methods indicated that these results could begeneralised to the population of the United Kingdom.* see PharmacoEconomics & Outcomes News 189:8,21 Nov1998; 800683126

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PharmacoEconomics & Outcomes News 9 Jan 1998 No. 194