Comparison of single-dose meperidine, butorphanol, and dihydroergotamine in the treatment of vascular headache.

Abstract:

:We treated 64 emergency room patients with a primary vascular headache with dihydroergotamine (DHE), meperidine, or butorphanol. Post-treatment pain scores were lowest in the DHE group (p less than 0.01). Eight of 21 patients receiving DHE had greater than 90% reduction in pain compared with three of 19 patients receiving butorphanol and none of 22 receiving meperidine.

journal_name

Neurology

journal_title

Neurology

authors

Belgrade MJ,Ling LJ,Schleevogt MB,Ettinger MG,Ruiz E

doi

10.1212/wnl.39.4.590

subject

Has Abstract

pub_date

1989-04-01 00:00:00

pages

590-2

issue

4

eissn

0028-3878

issn

1526-632X

journal_volume

39

pub_type

临床试验,杂志文章
  • Sensitivity and specificity of transcranial Doppler ultrasonography in the diagnosis of vasospasm following subarachnoid hemorrhage.

    abstract::Vasospasm is the leading cause of death and disability in patients with aneurysmal subarachnoid hemorrhage (SAH). Transcranial Doppler ultrasonography (TCD) can detect the arterial narrowing noninvasively, but the sensitivity and specificity of this technique have not been reported in a population of patients with a h...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.39.11.1514

    authors: Sloan MA,Haley EC Jr,Kassell NF,Henry ML,Stewart SR,Beskin RR,Sevilla EA,Torner JC

    更新日期:1989-11-01 00:00:00

  • Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations.

    abstract:OBJECTIVE:To describe the phenotype and phenotype-genotype correlations in patients with amyotrophic lateral sclerosis (ALS) with TARDBP gene mutations. METHODS:French TARDBP+ patients with ALS (n = 28) were compared first to 3 cohorts: 737 sporadic ALS (SALS), 192 nonmutated familial ALS (FALS), and 58 SOD1 + FALS, a...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3182553c88

    authors: Corcia P,Valdmanis P,Millecamps S,Lionnet C,Blasco H,Mouzat K,Daoud H,Belzil V,Morales R,Pageot N,Danel-Brunaud V,Vandenberghe N,Pradat PF,Couratier P,Salachas F,Lumbroso S,Rouleau GA,Meininger V,Camu W

    更新日期:2012-05-08 00:00:00

  • Prevalence of mild cognitive impairment is higher in men. The Mayo Clinic Study of Aging.

    abstract:OBJECTIVE:We investigated the prevalence of mild cognitive impairment (MCI) in Olmsted County, MN, using in-person evaluations and published criteria. METHODS:We evaluated an age- and sex-stratified random sample of Olmsted County residents who were 70-89 years old on October 1, 2004, using the Clinical Dementia Ratin...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181f11d85

    authors: Petersen RC,Roberts RO,Knopman DS,Geda YE,Cha RH,Pankratz VS,Boeve BF,Tangalos EG,Ivnik RJ,Rocca WA

    更新日期:2010-09-07 00:00:00

  • Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markers.

    abstract::We previously reported a large Charcot-Marie-Tooth family not linked to the Duffy blood group marker, supporting the existence of genetic heterogeneity in this neuropathy. In order to investigate the possibility of another disease locus on chromosome 1, we analyzed this family further, using DNA polymorphisms of 6 gen...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.39.6.844

    authors: Raeymaekers P,De Jonghe P,Backhovens H,Wehnert A,De Winter G,Swerts L,Gheuens J,Martin JJ,Vandenberghe A,Van Broeckhoven C

    更新日期:1989-06-01 00:00:00

  • Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.

    abstract:BACKGROUND:Paroxysmal nonkinesigenic dyskinesia (PNKD) is a rare disorder characterized by episodic hyperkinetic movement attacks. We have recently identified mutations in the MR-1 gene causing familial PNKD. METHODS:We reviewed the clinical features of 14 kindreds with familial dyskinesia that was not clearly induced...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000262029.91552.e0

    authors: Bruno MK,Lee HY,Auburger GW,Friedman A,Nielsen JE,Lang AE,Bertini E,Van Bogaert P,Averyanov Y,Hallett M,Gwinn-Hardy K,Sorenson B,Pandolfo M,Kwiecinski H,Servidei S,Fu YH,Ptácek L

    更新日期:2007-05-22 00:00:00

  • Evaluation of ambulatory cassette EEG monitoring: III. Diagnostic accuracy compared to intensive inpatient EEG monitoring.

    abstract::We assessed the ability to recognize epileptiform abnormalities on a video review of ambulatory cassette EEGs (A/EEG) by comparing two independent interpretations of an A/EEG to those derived from a routine recording and intensive monitoring by cable telemetry (C/EEG) of the same 40 patients. Both A/EEG readings concu...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.33.7.853

    authors: Ebersole JS,Leroy RF

    更新日期:1983-07-01 00:00:00

  • Effects of oral choline on human complex partial seizures.

    abstract::We carried out an open study of the effects of large doses (12 to 16 gm per day) of oral choline on medically intractable human complex partial seizures (CPS). Marked increases of plasma choline concentration (75 to 300%) in three subjects were associated with (1) shorter duration of CPS, (2) less postseizure fatigue,...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.30.12.1334

    authors: McNamara JO,Carwile S,Hope V,Luther J,Miller P

    更新日期:1980-12-01 00:00:00

  • Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood.

    abstract:OBJECTIVE:The natural history of succinic semialdehyde dehydrogenase (SSADH) deficiency in adulthood is unknown; we elucidate the clinical manifestations of the disease later in life. METHODS:A 63-year-old man with long-standing intellectual disability was diagnosed with SSADH deficiency following hospitalization for ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000001906

    authors: Lapalme-Remis S,Lewis EC,De Meulemeester C,Chakraborty P,Gibson KM,Torres C,Guberman A,Salomons GS,Jakobs C,Ali-Ridha A,Parviz M,Pearl PL

    更新日期:2015-09-08 00:00:00

  • Restless legs syndrome: treatment with dopaminergic agents.

    abstract::Restless legs syndrome (RLS) is a common neurologic disorder that affects 5 to 10% of the population and increases in prevalence with aging. The clinical hallmarks of RLS include dysesthesias or paresthesias in the legs and sometimes the arms, occurring primarily at rest, which are usually worse in the evening and are...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/wnl.58.suppl_1.s87

    authors: Comella CL

    更新日期:2002-02-26 00:00:00

  • Hereditary neuropathy with upper motor-neuron, visual pathway, and autonomic disorders.

    abstract::A 42-year-old man had progressive distal weakness and muscle atrophy, stocking-type sensory loss, upper motor-neuron and visual pathway lesions, and dysautonomia. Electrodiagnostic tests revealed a generalized sensorimotor peripheral neuropathy that largely involved axons. Low recumbent and upright norepinephrine leve...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.33.11.1495

    authors: Rechthand E,Reife R,Kaplan JG

    更新日期:1983-11-01 00:00:00

  • New NBIA subtype: genetic, clinical, pathologic, and radiographic features of MPAN.

    abstract:OBJECTIVE:To assess the frequency of mutations in C19orf12 in the greater neurodegeneration with brain iron accumulation (NBIA) population and further characterize the associated phenotype. METHODS:Samples from 161 individuals with idiopathic NBIA were screened, and C19orf12 mutations were identified in 23 subjects. D...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31827e07be

    authors: Hogarth P,Gregory A,Kruer MC,Sanford L,Wagoner W,Natowicz MR,Egel RT,Subramony SH,Goldman JG,Berry-Kravis E,Foulds NC,Hammans SR,Desguerre I,Rodriguez D,Wilson C,Diedrich A,Green S,Tran H,Reese L,Woltjer RL,Hayfli

    更新日期:2013-01-15 00:00:00

  • Multifocal independent epileptiform discharges in children: ictal correlates and surgical therapy.

    abstract::We obtained continuous EEG/video recordings on four children who had the interictal EEG pattern of multifocal independent epileptiform discharges (MIED). The prominent feature of their evaluation was the evidence that their clinical seizures appeared to be of focal origin; 42/44 seizures were manifested by "fencing po...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.41.8.1223

    authors: Burnstine TH,Vining EP,Uematsu S,Lesser RP

    更新日期:1991-08-01 00:00:00

  • Relationship of UV exposure to prevalence of multiple sclerosis in England.

    abstract:OBJECTIVE:To assess the potential relationship of ultraviolet B radiation (UVB) and Epstein-Barr virus (EBV) exposure in explaining the period prevalence of multiple sclerosis (MS) in England. METHODS:English national Hospital Episode Statistics covering all admissions to National Health Service hospitals in England i...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e318216715e

    authors: Ramagopalan SV,Handel AE,Giovannoni G,Rutherford Siegel S,Ebers GC,Chaplin G

    更新日期:2011-04-19 00:00:00

  • Abeta1-42 promotes cholinergic sprouting in patients with AD and Lewy body variant of AD.

    abstract:BACKGROUND:The neurodegenerative process in Alzheimer's disease (AD) and in the Lewy body variant of AD (LBV) patients is characterized by cholinergic dysfunction and deposition of amyloid beta-peptide (Abeta) 1-40 and 1-42; however, the differential effects of Abeta species on the cholinergic system are not completely...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000073987.79060.4b

    authors: Masliah E,Alford M,Adame A,Rockenstein E,Galasko D,Salmon D,Hansen LA,Thal LJ

    更新日期:2003-07-22 00:00:00

  • Multiple sclerosis prevalence in the United States commercially insured population.

    abstract:OBJECTIVE:To estimate the US commercially insured multiple sclerosis (MS) annual prevalence from 2008 to 2012. METHODS:The study was a retrospective analysis using PharMetrics Plus, a nationwide claims database for over 42 million covered US representative lives. Annual point prevalence required insurance eligibility ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000002469

    authors: Dilokthornsakul P,Valuck RJ,Nair KV,Corboy JR,Allen RR,Campbell JD

    更新日期:2016-03-15 00:00:00

  • Hepatic ketogenesis and muscle carnitine deficiency.

    abstract::The levels of plasma free carnitine and ketone bodies have been found to fluctuate inversely in fasting individuals without muscle disease. Circulating short-chain acyl-carnitines paralleled beta-hydroxybutyrate levels. A patient with lipid storage myopathy and muscle carnitine deficiency, and his two daughters, devel...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.29.6.780

    authors: DiDonato S,Cornelio F,Storchi G,Rimoldi M

    更新日期:1979-06-01 00:00:00

  • Correlation of enzyme-inducing anticonvulsant use with outcome of patients with glioblastoma.

    abstract:BACKGROUND:Clinical trials involving patients with glioblastoma (GBM) distinguish cohorts who are treated with enzyme-inducing anticonvulsants (EIAC). Such anticonvulsants induce hepatic P450 microsomal enzymes, which accelerate the metabolism of certain chemotherapy and molecular targeted agents. However, the resultan...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181bbfeca

    authors: Jaeckle KA,Ballman K,Furth A,Buckner JC

    更新日期:2009-10-13 00:00:00

  • Neutralizing antibodies against HTLV-I in HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP) patients and asymptomatic carriers.

    abstract::We tested serum specimens from patients with HAM/TSP and asymptomatic HTLV-I carriers from endemic areas of Japan, Jamaica, Colombia, and Chile for neutralizing antibodies against HTLV-I. The data suggest a trend for neutralizing activity to be found more frequently in the sera from HAM/TSP patients than in sera from ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.42.11.2210

    authors: Minagawa H,Yoshida T,Itoyama Y,Mora CA,Albert P,Mori R

    更新日期:1992-11-01 00:00:00

  • Prognostic importance of brainstem auditory evoked responses after asphyxia.

    abstract::Brainstem auditory evoked responses were recorded after acute asphyxia in 126 infants, ages birth through 18 months. Of these, 21 had markedly abnormal amplitude ratios, and all infants with abnormal amplitude ratios had severe neurologic handicaps. An abnormal amplitude ratio predicts long-term neurologic sequelae of...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.31.11.1429

    authors: Hecox KE,Cone B

    更新日期:1981-11-01 00:00:00

  • Transient ischemic attacks: a prospective study of 225 patients.

    abstract::Between the years 1964 and 1973, 225 patients with transient ischemic attacks (TIAs) due primarily to atherosclerosis were evaluated and treated. They have now been followed for from 3 to 14 years (average 5.5 years). As of 1976, 82 of the 225 patients were dead, 21 from cerebral infarction, 52 from heart disease and ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.28.8.746

    authors: Toole JF,Yuson CP,Janeway R,Johnston F,Davis C,Cordell AR,Howard G

    更新日期:1978-08-01 00:00:00

  • Hospitalization in amyotrophic lateral sclerosis: causes, costs, and outcomes.

    abstract:OBJECTIVE:As ALS progresses, extensive supportive care is required, including multidisciplinary outpatient care and hospitalization. The authors studied the causes, health care utilization, and outcomes for hospitalized patients with ALS. METHODS:With use of the 1996 Nationwide Inpatient Sample, an administrative data...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.56.6.753

    authors: Lechtzin N,Wiener CM,Clawson L,Chaudhry V,Diette GB

    更新日期:2001-03-27 00:00:00

  • Treatment of Bell palsy with prednisone: a prospective, randomized study.

    abstract::Two hundred thirty-nine patients with Bell palsy were randomly distributed into prednisone-treated and control groups. Patients were followed until complete recovery or for 1 year. In the steroid-treated and control groups, respectively, incomplete recovery of facial strength occurred in 12 percent and 20 percent; mot...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1212/wnl.28.2.158

    authors: Wolf SM,Wagner JH,Davidson S,Forsythe A

    更新日期:1978-02-01 00:00:00

  • Mild cognitive impairment: incidence and vascular risk factors in a population-based cohort.

    abstract:OBJECTIVE:We examined the incidence of mild cognitive impairment (MCI) and its potential vascular risk factors in a prospective population-based study. METHODS:An age-stratified random population-based cohort (baseline n = 1,982), followed for up to 4 years, was annually assessed for cognitive and everyday functioning...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e318295d776

    authors: Ganguli M,Fu B,Snitz BE,Hughes TF,Chang CC

    更新日期:2013-06-04 00:00:00

  • Environmental risk factors and Parkinson's disease: a case-control study in Taiwan.

    abstract::To explore environmental risk factors for Parkinson's disease (PD) in Taiwan, we investigated 120 patients with PD and 240 hospital control subjects matched with patients on age (+/-2 years) and sex. Based on a structured open-ended questionnaire, we carried out standardized interviews to obtain history of exposure to...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.48.6.1583

    authors: Liou HH,Tsai MC,Chen CJ,Jeng JS,Chang YC,Chen SY,Chen RC

    更新日期:1997-06-01 00:00:00

  • A longitudinal study of brain atrophy in relapsing multiple sclerosis. The Multiple Sclerosis Collaborative Research Group (MSCRG).

    abstract:OBJECTIVE:To determine if progressive brain atrophy could be detected over 1- and 2-year intervals in relapsing MS, based on annual MR studies from the Multiple Sclerosis Collaborative Research Group (MSCRG) trial of interferon beta-1a (Avonex). METHODS:All subjects had mild to moderate disability, with baseline expan...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,多中心研究,随机对照试验

    doi:10.1212/wnl.53.1.139

    authors: Simon JH,Jacobs LD,Campion MK,Rudick RA,Cookfair DL,Herndon RM,Richert JR,Salazar AM,Fischer JS,Goodkin DE,Simonian N,Lajaunie M,Miller DE,Wende K,Martens-Davidson A,Kinkel RP,Munschauer FE 3rd,Brownscheidle CM

    更新日期:1999-07-13 00:00:00

  • Autoantibodies in postinfectious acute cerebellar ataxia.

    abstract::The authors found serum immunoglobulin M (IgM) autoantibody in a patient with typical acute cerebellar ataxia (ACA) and identified the antigen molecule as triosephosphate isomerase (TPI). TPI antigenicity to the patient's antibody was the highest in the cerebellar tissue. Eight of 23 patients with ACA had increased Ig...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000178802.38268.1e

    authors: Uchibori A,Sakuta M,Kusunoki S,Chiba A

    更新日期:2005-10-11 00:00:00

  • The impact of lesion side on acute stroke treatment.

    abstract:BACKGROUND:Only a small percentage of patients with acute stroke are treated with recombinant tissue plasminogen activator (rt-PA). OBJECTIVE:To investigate why patients with right-hemisphere strokes seem at high risk of not receiving rt-PA. METHODS:This study includes two phases. Phase 1: the authors compared demogr...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000167608.94237.aa

    authors: Di Legge S,Fang J,Saposnik G,Hachinski V

    更新日期:2005-07-12 00:00:00

  • Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination.

    abstract:OBJECTIVE:We investigated mitochondrial DNA (mtDNA) variants in children with a first episode of acquired demyelinating syndromes (PD-ADS) of the CNS and their relationship to disease phenotype, including subsequent diagnosis of multiple sclerosis (MS). METHODS:This exploratory analysis included the initial 213 childr...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31820ee1bb

    authors: Venkateswaran S,Zheng K,Sacchetti M,Gagne D,Arnold DL,Sadovnick AD,Scherer SW,Banwell B,Bar-Or A,Simon DK,Canadian Pediatric Demyelinating Disease Network.

    更新日期:2011-03-01 00:00:00

  • Mitochondrial DNA in migraine with aura.

    abstract::Migraine and the MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) syndrome have some clinical features in common. First, cerebral infarctions, most often in the posterior cerebral regions, which are a main symptom of MELAS, may complicate migraine. Second, migrainous headache w...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.46.6.1735

    authors: Klopstock T,May A,Seibel P,Papagiannuli E,Diener HC,Reichmann H

    更新日期:1996-06-01 00:00:00

  • Epilepsy in multiple sclerosis: A nationwide population-based register study.

    abstract:OBJECTIVE:To determine the cumulative incidence of epilepsy in a population-based cohort of patients with multiple sclerosis (MS) and to investigate the association between epilepsy and clinical features of MS. METHODS:All available patients in the Swedish MS register (n = 14,545) and 3 age- and sex-matched controls p...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000004740

    authors: Burman J,Zelano J

    更新日期:2017-12-12 00:00:00