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1.
Mult Scler ; 25(7): 987-993, 2019 06.
Article in English | MEDLINE | ID: mdl-29862891

ABSTRACT

BACKGROUND: The plant-based ω-3 fatty acid α-linolenic acid (ALA) has been associated with lower MS risk. It is currently unknown whether ALA affects disease activity. OBJECTIVE: To investigate the association between ALA levels and disease activity. METHODS: We conducted a cohort study including 87 multiple sclerosis (MS)-patients who originally participated in a randomized trial of ω-3 fatty acids (the OFAMS study). We measured serum levels of ALA during follow-up and used random intercept logistic regression to estimate odds ratios (OR) and 95% confidence intervals (CIs) for the association between ALA levels, new magnetic resonance imaging (MRI) lesions, Expanded Disability Status Scale (EDSS) progression and new relapses adjusting for age at inclusion, sex, and use of interferon beta-1a. RESULTS: In continuous (per 1-SD increase) multivariable-adjusted analyses, higher ALA levels were significantly associated with lower odds of new T2-lesions (OR: 0.59, 95% CI: 0.37-0.95) during follow-up. The effect estimates were similar for new T1Gd + lesions (OR: 0.73, 95% CI: 0.48-1.11), EDSS-progression (OR: 0.62, 95% CI: 0.34-1.16) and new relapses (OR: 0.49, 95% CI: 0.22-1.10), but these estimates did not reach statistical significance. Further adjustment for vitamin D and tobacco use did not materially change the results. CONCLUSION: We found that higher levels of ALA were associated with lower disease activity in MS-patients.


Subject(s)
Disease Progression , Multiple Sclerosis/blood , Multiple Sclerosis/pathology , Multiple Sclerosis/physiopathology , alpha-Linolenic Acid/blood , Adult , Female , Follow-Up Studies , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Randomized Controlled Trials as Topic , Severity of Illness Index
2.
BMC Neurol ; 16(1): 197, 2016 Oct 18.
Article in English | MEDLINE | ID: mdl-27756254

ABSTRACT

BACKGROUND: Leber's hereditary optic neuropathy (LHON) co-occuring with multiple sclerosis-like disease (LHON-MS) is suggested to be a separate disease entity denoted Harding's disease. Little is known about the response to initiation and discontinuation of potent immunomodulatory treatment in LHON-MS. CASE PRESENTATION: We describe a LHON-MS patient with 27 years disease duration who developed severe disease activity peaking 14 months after discontinuation of natalizumab, with extensive new inflammatory lesions throughout the brain and in the spinal cord resembling immune inflammatory reconstitution syndrome. She had previously been clinically and radiologically stable on natalizumab treatment for 6 years, and before that only experienced subtle clinical activity during 9 years on interferon beta1a. CONCLUSION: This is the first report on severe exacerbation of inflammatory disease activity after discontinuation of natalizumab in LHON-MS, and suggests that late rebound activity can occur in these patients.


Subject(s)
Inflammation/complications , Multiple Sclerosis/complications , Multiple Sclerosis/pathology , Natalizumab/administration & dosage , Natalizumab/therapeutic use , Optic Atrophy, Hereditary, Leber/complications , Optic Atrophy, Hereditary, Leber/pathology , Recurrence , Adult , Brain/pathology , Female , Humans , Inflammation/diagnostic imaging , Inflammation/pathology , Magnetic Resonance Imaging , Male , Multiple Sclerosis/diagnostic imaging , Multiple Sclerosis/drug therapy , Optic Atrophy, Hereditary, Leber/diagnostic imaging , Optic Atrophy, Hereditary, Leber/drug therapy , Spinal Cord/pathology , Time Factors
3.
BMC Health Serv Res ; 16(1): 552, 2016 10 06.
Article in English | MEDLINE | ID: mdl-27716390

ABSTRACT

BACKGROUND: Understanding the organisational set-up of physiotherapy services across different countries is increasingly important as clinicians around the world use evidence to improve their practice. This also has to be taken into consideration when multi-centre international clinical trials are conducted. This survey aimed to systematically describe organisational aspects of physiotherapy services for people with multiple sclerosis (MS) across Europe. METHODS: Representatives from 72 rehabilitation facilities within 23 European countries completed an online web-based questionnaire survey between 2013 and 2014. Countries were categorised according to four European regions (defined by United Nations Statistics). Similarities and differences between regions were examined. RESULTS: Most participating centres specialized in rehabilitation (82 %) and neurology (60 %), with only 38 % specialising in MS. Of these, the Western based Specialist MS centres were predominately based on outpatient services (median MS inpatient ratio 0.14), whilst the Eastern based European services were mostly inpatient in nature (median MS inpatient ratio 0.5). In almost all participating countries, medical doctors - specialists in neurology (60 %) and in rehabilitation (64 %) - were responsible for referral to/prescription of physiotherapy. The most frequent reason for referral to/prescription of physiotherapy was the worsening of symptoms (78 % of centres). Physiotherapists were the most common members of the rehabilitation team; comprising 49 % of the team in Eastern countries compared to approximately 30 % in the rest of Europe. Teamwork was commonly adopted; 86 % of centres based in Western countries utilised the interdisciplinary model, whilst the multidisciplinary model was utilised in Eastern based countries (p = 0.046). CONCLUSION: This survey is the first to provide data about organisational aspects of physiotherapy for people with MS across Europe. Overall, care in key organisational aspects of service provision is broadly similar across regions, although some variations, for example the models of teamwork utilised, are apparent. Organisational framework specifics should be considered anytime a multi-centre study is conducted and results from such studies are applied.


Subject(s)
Multiple Sclerosis/therapy , Physical Therapy Modalities/organization & administration , Ambulatory Care/statistics & numerical data , Europe , Humans , Inpatients , Patient Care Team/organization & administration , Prescriptions , Referral and Consultation/statistics & numerical data , Surveys and Questionnaires
4.
Neuropsychol Rehabil ; 25(1): 137-54, 2015.
Article in English | MEDLINE | ID: mdl-25356835

ABSTRACT

The aim of the study was to investigate the predictive value of important disease-related variables on goal attainment in cognitive rehabilitation in multiple sclerosis (MS). The possible predictive value of executive functions, neurological disability, depression and general cognitive ability was assessed, employing Goal Attainment Scaling (GAS). Fifty-seven patients with MS were assessed for executive functions, neurological disability, depression and general cognitive ability, and guided through the process of formulating GAS-goals for coping with cognitive challenges in everyday life during a four week in-patient cognitive rehabilitation programme. GAS-goal attainment was scored during biweekly follow-up calls in the first three months post-discharge from the rehabilitation centre, and finally at seven months after the start of the rehabilitation. Consistent with the first study hypothesis MS patients succeeded in formulating and achieving GAS goals for coping with cognitive problems in everyday life. The patients were able to maintain a satisfactory level of goal attainment from the first measurement point after six weeks to seven months after the start of the rehabilitation. However, contrary to the second hypothesis, attainment of GAS goals was not predicted by executive functions. Neither was it predicted by neurological disability, depression or general cognitive ability. The findings suggest that GAS may be a practical and robust method in cognitive rehabilitation in MS patients, regardless of important disease-related characteristics.


Subject(s)
Cognition Disorders/rehabilitation , Goals , Multiple Sclerosis/rehabilitation , Activities of Daily Living , Adaptation, Psychological , Cognition Disorders/complications , Disability Evaluation , Executive Function , Female , Humans , Male , Middle Aged , Multiple Sclerosis/complications , Psychological Tests , Treatment Outcome
5.
Mult Scler ; 20(14): 1833-40, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24842958

ABSTRACT

BACKGROUND: Previous reports indicate an association between Epstein-Barr virus (EBV) antibody levels and multiple sclerosis (MS) disease activity, but the results have been conflicting. OBJECTIVES: The objective of this paper is to study if EBV antibody levels reflect MRI disease activity in MS and examine the potential for EBV antibody levels as biomarkers for treatment response. METHODS: A total of 87 MS patients were followed for two years prior to and during interferon beta (IFNB) treatment, with MRI examinations and serum measurement of IgM and IgG antibodies to viral capsid antigen (VCA), EBV nuclear antigen 1 (EBNA-1) and early antigen (EA). Associations between EBV antibody levels and MRI activity were assessed by a logistic regression model. RESULTS: Higher anti-EBNA-1 IgG levels were associated with increased MRI activity, OR = 2.95 (95% CI 1.07-8.10; p = 0.036) for combined unique activity (CUA; the sum of T1Gd+ lesions and new or enlarging T2 lesions). Although most patients were anti-VCA IgM negative, there was an inverse association, OR = 0.32 (95% CI 0.12-0.84; p = 0.021) with CUA during IFNB treatment. CONCLUSIONS: This study supports an association between anti-EBNA-1 IgG levels and MS disease activity. We also found an inverse association with anti-VCA IgM levels during IFNB treatment not previously described, indicating anti-VCA IgM as a possible biomarker for IFNB treatment response.


Subject(s)
Antibodies, Viral/immunology , Brain/pathology , Herpesvirus 4, Human/immunology , Multiple Sclerosis/immunology , Adult , Antigens, Viral/immunology , Capsid Proteins/immunology , Epstein-Barr Virus Nuclear Antigens/immunology , Fatty Acids, Omega-3/therapeutic use , Female , Humans , Immunoglobulin G/immunology , Immunoglobulin M/immunology , Immunologic Factors/therapeutic use , Interferon beta-1a , Interferon-beta/therapeutic use , Magnetic Resonance Imaging , Male , Middle Aged , Multiple Sclerosis/drug therapy , Multiple Sclerosis/pathology , Prospective Studies , Severity of Illness Index
6.
Mult Scler ; 19(4): 451-7, 2013 Apr.
Article in English | MEDLINE | ID: mdl-22907941

ABSTRACT

BACKGROUND: Vitamin A has immunomodulatory properties and may regulate the transcription of genes involved in remyelination. OBJECTIVE: To investigate the association between retinol and disease activity in multiple sclerosis (MS). METHODS: Cohort study of 88 relapsing-remitting MS patients, originally included in a randomised placebo-controlled trial of omega-3 fatty acids in MS (the OFAMS study), followed prospectively for 24 months with repeated assessments of serum-retinol and magnetic resonance imaging (MRI). All patients were initiated on interferon ß-1a after month 6. RESULTS: Each 1 µmol/L increase in serum-retinol reduced the odds (95% confidence interval) for new T1 gadolinium enhanced (Gd(+)) lesions by 49 (8-70)%, new T2 lesions by 42 (2-66)%, and combined unique activity (CUA) by 46 (3-68)% in simultaneous MRI scans, and 63 (25-82)% for new T1Gd(+) lesions, 49 (3-73)% for new T2 lesions and 43 (12-71)% for CUA the subsequent month. Serum-retinol also predicted new T1Gd(+) and T2 lesions six months ahead. The associations were not affected by HLA-DRB1*15, or serum levels of 25-hydroxyvitamin D, eicosapentaenoic acid or docosahexaenoic acid. CONCLUSION: Serum retinol is inversely associated with simultaneous and subsequent MRI outcomes in RRMS.


Subject(s)
Multiple Sclerosis, Relapsing-Remitting/blood , Multiple Sclerosis, Relapsing-Remitting/pathology , Vitamin A/blood , Adult , Chromatography, High Pressure Liquid , Fatty Acids, Omega-3/therapeutic use , Female , Humans , Immunologic Factors/therapeutic use , Interferon-beta/therapeutic use , Magnetic Resonance Imaging , Male , Middle Aged , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Randomized Controlled Trials as Topic , Young Adult
7.
Tidsskr Nor Laegeforen ; 132(5): 523-6, 2012 Mar 06.
Article in English, Nor | MEDLINE | ID: mdl-22398768

ABSTRACT

BACKGROUND: The motor and non-motor symptoms of multiple sclerosis often result in a substantially reduced health-related quality of life. We surveyed patient satisfaction and own evaluation of the benefit of a period spent at a specialised rehabilitation centre. MATERIAL AND METHOD: All patients who spent a period at the Hakadal MS rehabilitation centre in 2010 were asked to complete a validated questionnaire designed to determine patient satisfaction with rehabilitation institutions. RESULTS: Of a total of 339 patients, 277 (82%) returned the questionnaire. The great majority of respondents were satisfied with the knowledge, cooperation, care and engagement of those providing treatment, as well as with the advance information provided and the premises. They also found that they were consulted concerning their rehabilitation programme and that they were prepared for the period following their stay. More than 85% of the respondents stated that the stay would have major or very great importance for their general qualify of life and physical health. A similar score for mental health was given by 83%, mastery of day-to-day tasks by 77% and participation in social activities by 71%. INTERPRETATION: Patients who have had stays at the Hakadal MS rehabilitation centre are satisfied and feel that the stay will be of great importance to their level of functioning and mastery.


Subject(s)
Multiple Sclerosis/rehabilitation , Patient Satisfaction , Activities of Daily Living , Adult , Female , Follow-Up Studies , Humans , Male , Middle Aged , Multiple Sclerosis/psychology , Norway , Program Evaluation , Quality of Life , Rehabilitation Centers , Surveys and Questionnaires
8.
Article in English | MEDLINE | ID: mdl-32023868

ABSTRACT

Background: Guidelines and general recommendations are available for multiple sclerosis rehabilitation, but no specific guidance exists for physical therapists. Describing aspects of physical therapy content and delivery in multiple sclerosis and its determinants and analysing whether general recommendations connected with physical therapy are implemented in practice is important for interpreting clinical and research evidence. Methods: An online cross-sectional survey of physical therapists specialized in multiple sclerosis (212 specialists from 26 European countries) was used. Results: There was distinct diversity in service delivery and content across Europe. Perceived accessibility of physical therapy varied from most accessible in the Western region, and least in the Southern region. Sixty-four physical therapists adjusted their approach according to different disability levels, less so in the Eastern region. Duration, frequency and dose of sessions differed between regions, being highest in Southern and Western regions. "Hands on treatment" was the most commonly used therapeutic approach in all apart from the Northern regions, where "word instruction" (providing advice and information) prevailed. Conclusions: The content and delivery of physical therapy differs across Europe. Recommendations concerning access to treatment and adjustment according to disability do not appear to be widely implemented in clinical practice.


Subject(s)
Delivery of Health Care , Multiple Sclerosis , Physical Therapy Modalities , Adult , Cross-Sectional Studies , Delivery of Health Care/statistics & numerical data , Europe , Female , Humans , Male , Middle Aged , Multiple Sclerosis/therapy , Surveys and Questionnaires , Young Adult
9.
Lancet Neurol ; 8(6): 519-29, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19409854

ABSTRACT

BACKGROUND: Treatment of relapsing-remitting multiple sclerosis with interferon beta is only partly effective, and new more effective and safe strategies are needed. Our aim was to assess the efficacy of oral methylprednisolone as an add-on therapy to subcutaneous interferon beta-1a to reduce the yearly relapse rate in patients with relapsing-remitting multiple sclerosis. METHODS: NORMIMS (NORdic trial of oral Methylprednisolone as add-on therapy to Interferon beta-1a for treatment of relapsing-remitting Multiple Sclerosis) was a randomised, placebo-controlled trial done in 29 neurology departments in Denmark, Norway, Sweden, and Finland. We enrolled outpatients with relapsing-remitting multiple sclerosis who had had at least one relapse within the previous 12 months despite subcutaneous interferon beta-1a treatment (44 microg three times per week). We randomly allocated patients by computer to add-on therapy of either 200 mg methylprednisolone or matching placebo, both given orally on 5 consecutive days every 4 weeks for at least 96 weeks. The primary outcome measure was mean yearly relapse rate. Primary analyses were by intention to treat. This trial is registered, number ISRCTN16202527. FINDINGS: 66 patients were assigned to interferon beta and oral methylprednisolone and 64 were assigned to interferon beta and placebo. A high proportion of patients withdrew from the study before week 96 (26% [17 of 66] on methylprednisolone vs 17% [11 of 64] on placebo). The mean yearly relapse rate was 0.22 for methylprednisolone compared with 0.59 for placebo (62% reduction, 95% CI 39-77%; p<0.0001). Sleep disturbance and neurological and psychiatric symptoms were the most frequent adverse events recorded in the methylprednisolone group. Bone mineral density had not changed after 96 weeks. INTERPRETATION: Oral methylprednisolone given in pulses every 4 weeks as an add-on therapy to subcutaneous interferon beta-1a in patients with relapsing-remitting multiple sclerosis leads to a significant reduction in relapse rate. However, because of the small number of patients and the high dropout rate, these findings need to be corroborated in larger cohorts.


Subject(s)
Adjuvants, Immunologic/therapeutic use , Glucocorticoids/therapeutic use , Interferon-beta/therapeutic use , Methylprednisolone/therapeutic use , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Adolescent , Adult , Antibodies/metabolism , Confidence Intervals , Disability Evaluation , Double-Blind Method , Drug Administration Routes , Drug Therapy, Combination , Europe , Female , Follow-Up Studies , Humans , Interferon beta-1a , Kaplan-Meier Estimate , Male , Middle Aged , Multiple Sclerosis, Relapsing-Remitting/immunology , Multiple Sclerosis, Relapsing-Remitting/physiopathology , Psychomotor Performance/drug effects , Psychomotor Performance/physiology , Retrospective Studies , Severity of Illness Index , Young Adult
10.
Tidsskr Nor Laegeforen ; 128(18): 2068-71, 2008 Sep 25.
Article in Nor | MEDLINE | ID: mdl-18846123

ABSTRACT

BACKGROUND: Early Parkinson's disease is dominated by a motor syndrome called parkinsonism, but as the disease develops motor complications and non-motor problems may occur as well. This paper describes how to diagnose Parkinson's disease and the various motor complications and gives recommendations on how to treat the symptoms in these patients. MATERIAL AND METHODS: The paper builds on international evidence-based publications and the Norwegian guidelines for treatment of Parkinson's disease. RESULTS AND INTERPRETATION: Motor symptoms such as tremor at rest, akinesia, rigidity and postural instability are the cardinal signs in Parkinson's disease. After diagnosing a patient with the disease we recommend to start with selegiline as a disease-modifying treatment strategy. When symptoms lead to functional impairment, symptomatic treatment should be started in addition. Dopamine agonists are primarily recommended in younger patients and levodopa in the older ones. When the patients develop motor complications it is important to first thoroughly evaluate the problems to arrive at the best possible treatment strategy. If a sufficient response is not obtained both deep brain stimulation and treatment with continuous delivery of medication should be considered.


Subject(s)
Dyskinesias/diagnosis , Parkinson Disease/physiopathology , Age Factors , Antiparkinson Agents/administration & dosage , Antiparkinson Agents/therapeutic use , Deep Brain Stimulation , Dopamine Agonists/administration & dosage , Dopamine Agonists/therapeutic use , Dyskinesias/complications , Dyskinesias/drug therapy , Dystonia/diagnosis , Dystonia/drug therapy , Humans , Levodopa/administration & dosage , Levodopa/therapeutic use , Muscle Rigidity/diagnosis , Muscle Rigidity/drug therapy , Parkinson Disease/complications , Parkinson Disease/diagnosis , Parkinson Disease/drug therapy , Selegiline/administration & dosage , Selegiline/therapeutic use , Treatment Outcome , Tremor/diagnosis , Tremor/drug therapy
11.
J Neuroimmunol ; 323: 73-77, 2018 10 15.
Article in English | MEDLINE | ID: mdl-30196837

ABSTRACT

Adipokines secreted by fatty tissue have inflammatory properties and are suggested biomarkers of MS disease activity. To assess this, 88 MS patients were followed with nine repeated measurements of leptin and adiponectin and 12 magnetic resonance imaging (MRI) scans for two years; six months without any immunomodulatory treatment followed by 18 months during interferon-beta (IFNB) treatment. Serum levels of leptin dropped and adiponectin increased upon initiation of IFNB-therapy, but were not associated with clinical or MRI disease activity or with treatment response. Our findings indicate that leptin and adiponectin are not useful as biomarkers of MS disease activity.


Subject(s)
Adiponectin/blood , Disease Progression , Interferon-beta/therapeutic use , Leptin/blood , Multiple Sclerosis/blood , Multiple Sclerosis/drug therapy , Biomarkers/blood , Cohort Studies , Double-Blind Method , Female , Humans , Immunologic Factors/therapeutic use , Magnetic Resonance Imaging/trends , Male , Multiple Sclerosis/diagnostic imaging , Prospective Studies , Treatment Outcome
12.
Mult Scler Relat Disord ; 22: 59-67, 2018 May.
Article in English | MEDLINE | ID: mdl-29579644

ABSTRACT

BACKGROUND: A wide variety of interventions exists in physical therapy (PT), but knowledge about their use across different geographical regions is limited. This study investigated the use of PT interventions in people with multiple sclerosis (MS) across Europe. It aimed to determine whether regions differ in applying interventions, and explore whether factors other than regions play a role in their use. METHODS: In an online cross-sectional survey, 212 respondents from 115 European workplaces providing PT services to people with MS representing 26 countries (four European regions) participated. Cluster analysis, Pearson Chi-squared test and a Poisson regression model were used to analyze the data. RESULTS: Thirteen of 45 listed PT interventions were used by more than 75% of centers, while nine interventions were used by less than 25%. For 12 interventions, regions differed markedly in their use. Cluster analysis of centers identified four clusters similar in their intervention use. Cluster assignment did not fully align with regions. While center region was important, center size, number and gender of physical therapists working in the center, and time since qualification also played a role. Cluster analysis exploring the use of the interventions provided the basis for a categorization of PT interventions in line with their primary focus: 1. Physical activity (fitness/endurance/resistance) training; 2. Neuroproprioceptive "facilitation/inhibition"; 3. Motor/skill acquisition (individualized therapy led); 4. Technology based interventions. CONCLUSIONS: To our knowledge this is the first study that has explored this topic in MS. The results broaden our understanding of the different PT interventions used in MS, as well as the context of their use.


Subject(s)
Multiple Sclerosis/therapy , Physical Therapy Modalities , Cluster Analysis , Cross-Sectional Studies , Europe , Female , Humans , Male , Regression Analysis
13.
14.
Neurol Neuroimmunol Neuroinflamm ; 3(4): e260, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27458599

ABSTRACT

OBJECTIVE: To study whether tobacco use is associated with MRI and clinical disease activity in patients with multiple sclerosis (MS). METHODS: Prospective cohort study of 87 patients with relapsing-remitting MS originally included in a randomized placebo-controlled trial of omega-3 fatty acids in MS (the OFAMS Study). Serum levels of cotinine (biomarker of tobacco use) were analyzed at baseline and every 6 months for 2 years. MRI activity was assessed at baseline and monthly for 9 months and after 12 and 24 months. RESULTS: Fifty-three patients (61%) had serum cotinine levels ≥85 nmol/L on ≥60% of the measurements and were considered tobacco users and 34 (39%) had cotinine levels <85 nmol/L, consistent with non-tobacco use. There was no association between tobacco use and the occurrence of new gadolinium-enhancing T1 lesions, new or enlarging T2 lesions, or their aggregate (combined unique activity). Furthermore, there was no association between cotinine levels and MRI activity for the tobacco users, and tobacco users did not have more relapses or Expanded Disability Status Scale progression. CONCLUSION: Our results indicate that tobacco use does not directly influence MRI activity or relapse rate in MS. This may implicate that the reported association between smoking and MS disease progression could be mediated through other mechanisms.

15.
Tidsskr Nor Laegeforen ; 125(19): 2638-40, 2005 Oct 06.
Article in Nor | MEDLINE | ID: mdl-16215609

ABSTRACT

BACKGROUND: The advanced stage of Parkinson's disease is characterised by motor fluctuations which are often difficult to control on traditional, peroral levodopa medication. We present our experience and a literature search regarding a method for continuous intraduodenal administration of a levodopa/carbidopa gel (Duodopa). METHODS: In a pilot study based on the compassionate use of continuous intraduodenal levodopa, patients were tested via nasoduodenal administration of the gel and on-off registration. For patients in whom a significant improvement in time in near-normal function per day was seen, permanent administration was started through a permanent duodenal port via percutaneous endoscopic gastrostomy with an inner catheter to the duodenal-jejunal transition. RESULTS AND CONCLUSION: In the nine patients tested, a significant functional improvement over time was seen. Five patients now have a permanent system with lasting good effect. Qualitative evaluation shows maintained good effect over a follow up time of up to 2.5 years (mean 19 months). We conclude that continuous enteral levodopa administration is a good and safe alternative especially for patients not offered deep brain stimulation. Its place among other treatment methods needs further assessment.


Subject(s)
Antiparkinson Agents/administration & dosage , Carbidopa/administration & dosage , Levodopa/administration & dosage , Parkinson Disease/drug therapy , Aged , Drug Combinations , Duodenum , Humans , Infusion Pumps , Middle Aged
16.
Tidsskr Nor Laegeforen ; 125(4): 425-8, 2005 Feb 17.
Article in Nor | MEDLINE | ID: mdl-15742012

ABSTRACT

A national group of neurologists and ophthalmologists have evaluated guidelines and recommendations for diagnosis, treatment and follow up of optic neuritis based on clinical experience and a review of relevant literature. Optic neuritis is a common, well characterised condition that appears as an isolated syndrome or as a manifestation of multiple sclerosis. Several other diseases must be considered for a differential diagnosis. Corticosteroid treatment of optic neuritis has been investigated in a number of trials, which show that corticosteroid treatment speeds up the recovery of vision without affecting the final visual outcome. The diagnostic procedure and the treatment options have changed over the last few years. Some aspects of investigation, treatment and follow up are still controversial.


Subject(s)
Optic Neuritis , Diagnosis, Differential , Follow-Up Studies , Glucocorticoids/therapeutic use , Humans , Magnetic Resonance Imaging , Methylprednisolone/therapeutic use , Multiple Sclerosis/etiology , Optic Neuritis/complications , Optic Neuritis/diagnosis , Optic Neuritis/drug therapy , Practice Guidelines as Topic , Risk Factors , Visual Acuity
17.
Mult Scler Int ; 2015: 317859, 2015.
Article in English | MEDLINE | ID: mdl-26221541

ABSTRACT

Objective. Patients with multiple sclerosis (MS) are often suffering from neuropathic pain. Antiepileptic drugs (AEDs) and tricyclic antidepressants (TCAs) are commonly used and are susceptible to be involved in drug interactions. The aim of this retrospective study was to investigate the prevalence of use of antiepileptic and antidepressive drugs in MS patients and to discuss the theoretical potential for interactions. Methods. Review of the medical records from all patients treated at a dedicated MS rehabilitation centre in Norway between 2009 and 2012. Results. In total 1090 patients attended a rehabilitation stay during the study period. Of these, 342 (31%; 249 females) with mean age of 53 (±10) years and EDSS 4.8 (±1.7) used at least one AED (gabapentin 12.7%, pregabalin 7.7%, clonazepam 7.8%, and carbamazepine 2.6%) or amitriptyline (9.7%). Polypharmacy was widespread (mean 5.4 drugs) with 60% using additional CNS-active drugs with a propensity to be involved in interactions. Age, gender, and EDSS scores did not differ significantly between those using and not using AED/amitriptyline. Conclusion. One-third of MS patients attending a rehabilitation stay receive AED/amitriptyline treatment. The high prevalence of polypharmacy and use of CNS-active drugs calls for awareness of especially pharmacodynamic interactions and possible excessive adverse effects.

18.
J Neuroimmunol ; 288: 92-7, 2015 Nov 15.
Article in English | MEDLINE | ID: mdl-26531700

ABSTRACT

Obesity is a possible risk factor of multiple sclerosis (MS), but the association between obesity and MS disease activity has not been explored. In a cohort of 86 MS patients, 80% of overweight or obese patients (BMI≥25kg/m(2)) had MRI activity compared to 48% of the normal-weight patients (BMI<25kg/m(2)) (p=0.001) during interferon-beta treatment. NEDA-status (no evidence of disease activity) was defined as a composite that consisted of absence of any relapses, sustained disability-progression and MRI-activity. Among normal-weight patients 26% obtained NEDA-status compared to only 13% of patients with BMI >25 (p=0.05). This may indicate that BMI affects interferon-beta treatment response.


Subject(s)
Immunologic Factors/therapeutic use , Interferon-beta/therapeutic use , Multiple Sclerosis, Relapsing-Remitting/complications , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Multiple Sclerosis, Relapsing-Remitting/pathology , Obesity/complications , Adolescent , Adult , Body Mass Index , Brain/pathology , Disease Progression , Double-Blind Method , Enzyme-Linked Immunosorbent Assay , Female , Humans , Inflammation/etiology , Inflammation/pathology , Magnetic Resonance Imaging , Male , Middle Aged , Young Adult
19.
J Neuroimmunol ; 280: 21-8, 2015 Mar 15.
Article in English | MEDLINE | ID: mdl-25773151

ABSTRACT

To explore if vitamin D modulates interferon-ß1a treatment effects in relapsing-remitting multiple sclerosis, we examined relationships between serum vitamin D and magnetic resonance imaging (MRI) activity and ten systemic inflammation markers in 88 patients, before and during treatment. Odds ratios for all MRI parameters were negatively associated with vitamin D levels before therapy, but converged to equally low values irrespective of vitamin D status during treatment. During therapy, similar alterations of MRI activity and inflammation markers were found across patients categorized by mean vitamin D values. This suggests that vitamin D status has no major influence on interferon-ß1a treatment effects.


Subject(s)
Adjuvants, Immunologic/therapeutic use , Interferon-beta/therapeutic use , Magnetic Resonance Imaging , Multiple Sclerosis, Relapsing-Remitting , Vitamin D/blood , Adolescent , Adult , Cytokines/blood , Female , Humans , Interferon beta-1a , Longitudinal Studies , Male , Middle Aged , Multiple Sclerosis, Relapsing-Remitting/blood , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Multiple Sclerosis, Relapsing-Remitting/pathology , Norway , Regression Analysis , Retrospective Studies , Time Factors , Young Adult
20.
J Neurol ; 261(12): 2438-45, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25270681

ABSTRACT

Advanced-stage Parkinson's disease (PD) strongly affects quality of life (QoL). Continuous intraduodenal administration of levodopa (IDL) is efficacious, but entails high costs. This study aims to estimate these costs in routine care. 10 patients with advanced-PD who switched from oral medication to IDL were assessed at baseline, and subsequently at 3, 6, 9 and 12 months follow-up. We used the Unified PD Rating Scale (UPDRS) for function and 15D for Quality of Life (QoL). Costs were assessed using quarterly structured patient questionnaires and hospital registries. Costs per quality adjusted life year (QALY) were estimated for conventional treatment prior to switch and for 1-year treatment with IDL. Probabilistic sensitivity analysis was based on bootstrapping. IDL significantly improved functional scores and was safe to use. One-year conventional oral treatment entailed 0.63 QALY while IDL entailed 0.68 (p > 0.05). The estimated total 1-year treatment cost was NOK419,160 on conventional treatment and NOK890,920 on IDL, representing a cost of NOK9.2 million (€1.18 mill) per additional QALY. The incremental cost per unit UPDRS improvement was NOK25,000 (€3,250). Medication was the dominant cost during IDL (45% of total costs), it represented only 6.4% of the total for conventional treatment. IDL improves function but is not cost effective using recommended thresholds for cost/QALY in Norway.


Subject(s)
Cost-Benefit Analysis/economics , Drug Costs , Levodopa/administration & dosage , Levodopa/economics , Parkinson Disease/drug therapy , Parkinson Disease/economics , Administration, Oral , Aged , Antiparkinson Agents/administration & dosage , Antiparkinson Agents/economics , Duodenum , Female , Humans , Intubation/methods , Male , Middle Aged , Norway , Quality of Life , Surveys and Questionnaires
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