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1.
Can J Neurol Sci ; 46(2): 243-247, 2019 03.
Article in English | MEDLINE | ID: mdl-30724154

ABSTRACT

INTRODUCTION: Lewis-Sumner syndrome (LSS) is a demyelinating peripheral neuropathy described in 1982. METHODS: We reviewed the charts of nine LSS patients in neurological care for their symptoms, response to different treatment regimens, and pattern of nerve involvement. RESULTS: One patient had an Adie's pupil. Every patient studied had median nerve involvement. Seven of nine patients required intravenous immunoglobulin (IVIg) therapy and all showed improvement with IVIg. Four of nine patients received oral steroid therapy and had some improvement. Two of nine patients received azathioprine to little effect. Two of nine patients experienced significant trauma while receiving neurological follow-up and their symptoms worsened to a clinically significant degree afterward. DISCUSSION: We noticed a possible association between trauma and symptom severity in cases of LSS with preexisting neurological follow-up. We hypothesize that physical trauma exacerbates LSS. To our knowledge, this is an unreported phenomenon.


Subject(s)
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/diagnosis , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/physiopathology , Severity of Illness Index , Wounds and Injuries/diagnosis , Adult , Electrodiagnosis/methods , Female , Humans , Immunoglobulins, Intravenous/administration & dosage , Male , Middle Aged , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/therapy , Wounds and Injuries/physiopathology , Wounds and Injuries/therapy
2.
BMC Public Health ; 15: 620, 2015 Jul 07.
Article in English | MEDLINE | ID: mdl-26149681

ABSTRACT

BACKGROUND: Home visiting programs focused on improving early childhood environments are commonplace in North America. A goal of many of these programs is to improve the overall health of children, including promotion of age appropriate vaccination. In this study, population-based data are used to examine the effect of a home visiting program on vaccination rates in children. METHODS: Home visiting program data from Manitoba, Canada were linked to several databases, including a provincial vaccination registry to examine vaccination rates in a cohort of children born between 2003 and 2009. Propensity score weights were used to balance potential confounders between a group of children enrolled in the program (n = 4,562) and those who were eligible but not enrolled (n = 5,184). Complete and partial vaccination rates for one and two year old children were compared between groups, including stratification into area-level income quintiles. RESULTS: Complete vaccination rates from birth to age 1 and 2 were higher for those enrolled in the Families First program [Average Treatment Effect Risk Ratio (ATE RR) 1.06 (95 % CI 1.03-1.08) and 1.10 (95 % CI 1.05-1.15) respectively]. No significant differences were found between groups having at least one vaccination at age 1 or 2 [ATE RR 1.01 (95 % CI 1.00-1.02) and 1.00 (95 % CI 1.00-1.01) respectively). The interaction between program and income quintiles was not statistically significant suggesting that the program effect did not differ by income quintile. CONCLUSIONS: Home visiting programs have the potential to increase vaccination rates for children enrolled, despite limited program content directed towards this end. Evidence-based program enhancements have the potential to increase these rates further, however more research is needed to inform policy makers of optimal approaches in this regard, especially with respect to cost-effectiveness.


Subject(s)
House Calls/statistics & numerical data , Vaccination/statistics & numerical data , Child, Preschool , Cohort Studies , Female , Health Services Needs and Demand , Humans , Infant , Male , Manitoba , Socioeconomic Factors
3.
Clin Infect Dis ; 59(5): 651-7, 2014 Sep 01.
Article in English | MEDLINE | ID: mdl-24842908

ABSTRACT

BACKGROUND: In 2010, Winnipeg, Canada, experienced a doubling of invasive pneumococcal disease (IPD) rates, with a significant increase in the number of cases due to Streptococcus pneumoniae serotype 12F, which previously had accounted for very few cases each year. METHODS: All serotype 12F IPD cases reported between September 2009 and January 2011 were reviewed. Pulsed-field gel electrophoresis (PFGE) and multilocus variable number tandem repeat analysis (MLVA) were conducted on all isolates. PFGE and MLVA patterns identified several possible clusters. Additional interviews were conducted to obtain information on risk factors and outcomes. RESULTS: Between September 2009 and January 2011, 169 cases of IPD were identified. The number of IPD cases due to 12F serotype increased sharply from about 3-4 cases per year (6% of IPD cases) in 2007-2009 to 28 (29%) in 2010. All 12F isolates belonged to a single sequence type (ST218), and they were generally susceptible to penicillin and fluoroquinolones but not to erythromycin. Compared with cases caused by other serotypes, patients with serotype 12F were more likely to be homeless, reside in low-income inner-city communities, and engage in substance abuse, including intravenous and crack cocaine use. Subclusters identified using MLVA had even higher rates of homelessness and substance use. CONCLUSIONS: An immunization campaign targeting high-risk groups was undertaken with pneumococcal polysaccharide vaccine, and subsequently rates of serotype 12F decreased. To our knowledge, this is the largest documented community outbreak of serotype 12F IPD and the first report of an outbreak of IPD serotype 12F in a marginalized urban population in Canada.


Subject(s)
Disease Outbreaks , Pneumococcal Infections/epidemiology , Poverty , Streptococcus pneumoniae/classification , Adolescent , Adult , Aged , Canada/epidemiology , Child , Electrophoresis, Gel, Pulsed-Field , Female , Ill-Housed Persons , Humans , Male , Middle Aged , Pneumococcal Infections/microbiology , Pneumococcal Vaccines/administration & dosage , Pneumococcal Vaccines/immunology , Serogroup , Serotyping , Streptococcus pneumoniae/genetics , Streptococcus pneumoniae/isolation & purification , Substance-Related Disorders , Urban Population , Vaccination , Young Adult
4.
CNS Spectr ; 13(7 Suppl 11): 15-21, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18622370

ABSTRACT

There is evidence that the serotonin norepinephrine reuptake inhibitors (SNRIs) venlafaxine, milnacipran, and duloxetine, have probable superior antidepressant activity to most selective serotonin reuptake inhibitors (SSRIs), especially in more severe depression. Some patients, however, respond better than others to SNRIs. Several factors influencing response to milnacipran have been recently studied. The presence of certain polymorphisms related to noradrenergic neurotransmission has been shown to be related to different degrees or rapidity of response to milnacipran. In addition, patients with low pretreatment levels of plasma 3-methoxy-4-hydroxyphenylglycol have a better response to milnacipran. These recent genomic and neurochemical data confirm that milnacipran, in contrast to SSRIs and venlafaxine, has an impact on the noradrenergic system. Differences in metabolism determined by genetic variables in cytochrome P450 (CYP) 2D6 activity are a major determinant of venlafaxine levels to such an extent that genetically determined decreases in CYP 2D6 activity have been associated increased adverse effects. Milnacipran, which is not metabolized by the enzymes of the CYP system is not influenced by polymorphism of these enzymes. These preliminary data suggest that a patient's biochemical and pharmacogenetic characteristics may be useful in the future to help clinicians chose the most effective antidepressant medication.


Subject(s)
Depression/drug therapy , Depression/genetics , Pharmacogenetics , Selective Serotonin Reuptake Inhibitors/therapeutic use , Cyclopropanes/therapeutic use , Cytochrome P-450 CYP2D6/genetics , Depression/blood , Humans , Meta-Analysis as Topic , Methoxyhydroxyphenylglycol/blood , Milnacipran , Polymorphism, Genetic/genetics
5.
J Epidemiol Community Health ; 72(1): 47-53, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29122995

ABSTRACT

BACKGROUND: Home visiting has been shown to reduce child maltreatment and improve child health outcomes. In this observational study, we explored whether Families First, a home visiting programme in Manitoba, Canada, decreased population-level inequities in children being taken into care of child welfare and receiving complete childhood immunisations. METHODS: De-identified administrative health and social services data for children born 2003-2009 in Manitoba were linked to home visiting programme data. Programme eligibility was determined by screening for family risk factors. We compared probabilities of being taken into care and receiving immunisations among programme children (n=4575), eligible children who did not receive the programme (n=5186) and the general child population (n=87 897) and tested inequities using differences of risk differences (DRDs) and ratios of risk ratios (RRRs). RESULTS: Programme children were less likely to be taken into care (probability (95% CI) at age 1, programme 7.5 (7.0 to 8.0) vs non-programme 10.0 (10.0 to 10.1)) and more likely to receive complete immunisations (probability at age 1, programme 77.3 (76.5 to 78.0) vs non-programme 73.2 (72.1 to 74.3)). Inequities between programme children and the general population were reduced for both outcomes (being taken into care at age 1, DRD -2.5 (-3.7 to 1.2) and RRR 0.8 (0.7 to 0.9); complete immunisation at age 1, DRD 4.1 (2.2 to 6.0) and RRR 1.1 (1.0 to 1.1)); these inequities were also significantly reduced at age 2. CONCLUSION: Home visiting programmes should be recognised as effective strategies for improving child outcomes and reducing population-level health and social inequities.


Subject(s)
Child Abuse/prevention & control , Child Health , Child Welfare , Immunization , Postnatal Care/standards , Program Evaluation/methods , Canada , Child , Child, Preschool , Cohort Studies , Female , Health Status , Humans , Infant , Male , Population Surveillance , Retrospective Studies
6.
IDCases ; 8: 14-16, 2017.
Article in English | MEDLINE | ID: mdl-28271044

ABSTRACT

The global re-emergence of syphilis is an exigent public health issue requiring both clinicians and public health practitioners to become familiar with the myriad manifestations of this great imitator. This report describes a case of an originally undiagnosed chronic oral syphilitic chancre, subsequently confirmed by both PCR and immunohistochemistry.

7.
Child Maltreat ; 22(2): 121-131, 2017 05.
Article in English | MEDLINE | ID: mdl-28413917

ABSTRACT

While home visiting programs are among the most widespread interventions to support at-risk families, there is a paucity of research investigating these programs under real-world conditions. The effectiveness of Families First home visiting (FFHV) was examined for decreasing rates of being in care of child welfare, decreasing hospitalizations for maltreatment-related injuries, and improving child development at school entry. Data for 4,562 children from home visiting and 5,184 comparison children were linked to deidentified administrative health, social services, and education data. FFHV was associated with lower rates of being in care by child's first, second, and third birthday (adjusted risk ratio [aRR] = 0.75, 0.79, and 0.81, respectively) and lower rates of hospitalization for maltreatment-related injuries by third birthday (aRR = 0.59). No differences were found in child development at kindergarten. FFHV should be offered to at-risk families to decrease child maltreatment. Program enhancements are required to improve child development at school entry.


Subject(s)
Child Abuse/prevention & control , Child Development , Family Therapy/methods , House Calls , Age Factors , Child , Child Welfare , Child, Preschool , Female , Humans , Male , Program Evaluation , Retrospective Studies , Young Adult
16.
Can J Psychiatry ; 54(4): 260-8, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19321032

ABSTRACT

OBJECTIVE: Suicide prevention remains a challenge across communities in North America and abroad. We examine a suicide prevention effort that is widely used, termed gatekeeper training. There are 2 aims: review the state of the evidence on gatekeeper training for suicide prevention, and propose directions for further research. METHOD: Studies were identified by searching MEDLINE (PubMed) and PsycINFO from inception to the present for the key words suicide, suicide prevention, and gatekeeper. In addition, a manual scan of relevant articles' bibliographies was undertaken. RESULTS: Gatekeeper training has been implemented and studied in many populations, including military personnel, public school staff, peer helpers, clinicians, and Aboriginal people. This type of training has been shown to positively affect the knowledge, skills, and attitudes of trainees regarding suicide prevention. Large-scale cohort studies in military personnel and physicians have reported promising results with a significant reduction in suicidal ideation, suicide attempts, and deaths by suicide. CONCLUSIONS: Gatekeeper training is successful at imparting knowledge, building skills, and molding the attitudes of trainees; however, more work needs to be done on longevity of these traits and referral patterns of gatekeepers. There is a need for randomized controlled trials. In addition, the unique effect of gatekeeper training on suicide rates needs to be fully elucidated.


Subject(s)
Allied Health Occupations/education , Gatekeeping , Preventive Health Services/methods , Suicide Prevention , Adolescent , Adolescent Behavior , Humans , Male , Risk Factors , Suicide, Attempted/prevention & control
17.
Hum Psychopharmacol ; 20(3): 207-10, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15682431

ABSTRACT

BACKGROUND: Cannabis use is a major problem in inner cities and has been causally implicated in psychosis. Very few of the available hospital-based studies of the implications of cannabis usage have involved psychiatric intensive care units (PICU); but PICU receive many of the most challenging and resource-hungry-and incompletely understood-patients in the mental health system. AIMS: To study the clinical impact of cannabis abuse in a PICU, and to compare the use of atypical and typical antipsychotics in this setting. METHOD: 115 patients admitted to a PICU consented to take part in an open label naturalistic study. BPRS, TCI-240, weight, length of admission and routine bloods were evaluated in all participants. RESULTS: There was a high rate of cannabis abuse (71.3%) in the PICU population. Patients who abused cannabis spent longer in PICU because their psychoses were more severe. They were younger at first hospital admission. Cannabis also had metabolic implications, with higher blood glucose levels at admission and greater weight increase. Atypical antipsychotics were effective in treating psychosis inpatients positive to cannabis at admission. CONCLUSION: Our findings suggest that cannabis abusers had a more severe psychotic illness, especially in schizophrenia. There are additional complications in terms of weight gain for cannabis users.


Subject(s)
Antipsychotic Agents/pharmacology , Cannabis , Psychotic Disorders/drug therapy , Adult , Critical Care , Female , Humans , London/epidemiology , Male , Marijuana Abuse/epidemiology , Marijuana Abuse/psychology , Prospective Studies , Psychiatric Status Rating Scales , Psychotic Disorders/epidemiology , Psychotic Disorders/psychology , Risk Assessment , Substance Abuse Detection
18.
COPD ; 2(2): 233-41, 2005 Jun.
Article in English | MEDLINE | ID: mdl-17136950

ABSTRACT

The aim of this study was to determine whether treating concomitant depression improves quality of life and exercise tolerance in COPD patients. Out-patients with moderate to severe, stable COPD completed Hospital Anxiety-Depression (HAD) and General Health questionnaires. A psychiatrist interviewed those with high scores. In a randomised, double-blind fashion, 28 depressed COPD patients took a selective serotonin re-uptake inhibitor, Paroxetine 20 mg daily, or matched placebo for 6 weeks. Subsequently, all patients took un-blinded Paroxetine for 3 months. From these questionnaires, 35% of 135 patients had significant depression, but this was confirmed by psychiatric interview in only 21%. Throughout the study, there were no changes in laboratory lung function nor in home peak flow. Six weeks' treatment produced no significant differences between placebo and treatment group in either depression, quality of life scores or 6-minute walking distances, although overall improvements in depression, correlated with increases in walking distance. Three months of un-blinded treatment, significantly improved depression scores (self-complete HAD, Beck's Depression and psychiatrist-completed Montgomery-Asberg scores), walking distances (369 to 427 m, p = 0.0003) and St. George's Respiratory Questionnaire Total Scores (65 to 58, p = 0.033). Although self-complete questionnaires over-diagnose depression, the condition is nevertheless common in patients with moderately severe COPD. Six weeks of antidepressants is insufficient to improve either depression, quality of life or exercise tolerance. However, our study suggests that a longer course of treatment may be effective and that improvements in depression are associated with improvements in exercise tolerance. A larger, double blind study with a longer treatment period is indicated.


Subject(s)
Depressive Disorder/drug therapy , Exercise Tolerance/physiology , Pulmonary Disease, Chronic Obstructive/physiopathology , Pulmonary Disease, Chronic Obstructive/psychology , Quality of Life , Selective Serotonin Reuptake Inhibitors/therapeutic use , Aged , Depressive Disorder/etiology , Depressive Disorder/physiopathology , Double-Blind Method , Female , Humans , Male , Middle Aged , Respiratory Function Tests
19.
Hum Psychopharmacol ; 18(7): 569-74, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14533141

ABSTRACT

OBJECTIVE: Evidence that pindolol accelerates the action of antidepressants has been contradictory, and it is not clear why. The present study analyses the relationship between plasma prolactin (PRL) and ACTH levels and changes in relation to a milnacipran and pindolol combination versus milnacipran plus placebo. METHOD: Eighty depressed patients agreed to take part in a double-blind randomized trial of milnacipran plus pindolol or placebo. Fifty-eight of them agreed to also take measures of ACTH and PRL levels. ACTH and PRL plasma levels were estimated on days 0 and 42 of the 6-week study. Age, gender and time of blood collection were recorded for each individual. The Montgomery-Asberg depression rating scale (MADRS) was used to measure the response to treatment. The patients were grouped into those with higher versus lower basal ACTH levels using the median of the sample (25 ng/l). RESULTS: There were statistical differences in MADRS scores between the treatment groups on day 42. There were correlations between PRL levels on days 0 and 42; age and PRL levels on day 0; time of the PRL sample and the PRL levels on day 0 and day 42; ACTH and PRL levels on day 42. Regression analysis of the 58 patients showed that on day 0, PRL levels were dependent on the ACTH plasma levels on day 0, the time of the collection of the blood sample and the age. On day 42, the PRL levels were dependent on the ACTH levels and the time of the blood collection but not on the age. Patients with lower baseline ACTH levels on day 0 displayed a better clinical outcome when taking the combination of milnacipran and pindolol as shown in the differences in MADRS on day 42. The same group of patients showed lower PRL levels on day 42. CONCLUSIONS: ACTH plasma levels at baseline or screening may help to predict the response to antidepressant treatment.


Subject(s)
Adrenergic Agents/pharmacology , Adrenocorticotropic Hormone/blood , Cyclopropanes/pharmacology , Pindolol/pharmacology , Prolactin/blood , Serotonin Agents/pharmacology , Adrenergic Agents/therapeutic use , Adult , Age Factors , Cyclopropanes/therapeutic use , Depressive Disorder/drug therapy , Double-Blind Method , Drug Synergism , Drug Therapy, Combination , Female , Humans , Male , Milnacipran , Pindolol/therapeutic use , Psychiatric Status Rating Scales , Regression Analysis , Serotonin Agents/therapeutic use , Time Factors , Treatment Outcome
20.
Hum Psychopharmacol ; 18(8): 595-601, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14696018

ABSTRACT

BACKGROUND: New, better tolerated and faster treatments for depression are needed. Patients are understandably unhappy with having to wait 3 to 4 weeks for a response to an antidepressant, while experiencing side effects almost immediately. This frequently has an adverse effect on compliance and engagement with treatment. AIMS: The primary objective was to assess the activity of pindolol on the onset of antidepressive response of milnacipran. The secondary objective was to assess the number of responders among the patients who received milnacipran and pindolol versus patients who received milnacipran and placebo. The tertiary objective was to evaluate the safety of milnacipran and pindolol versus milnacipran and placebo. METHOD: Randomized, double-blind, placebo-controlled study over 42 days. SETTING: Inner city London community mental health teams. PARTICIPANTS: 80 patients were selected and gave written consent to treatment, 78 were randomized (39 in each group) and evaluated for safety (intention-to-treat, ITT, safety data set), 77 (ITT efficacy data set), and 64 (per protocol, PP, data set) were evaluated for efficacy. The mean age was 31.9 for the pindolol group and 32.3 for the placebo. INTERVENTION: All patients received milnacipran 50 mg twice a day plus either pindolol 2.5 mg (the 'pindolol group') or matching placebo (the 'placebo group') three times a day. OUTCOME MEASURES: The main efficacy variable was the Montgomery-Asberg depression rating scale (MADRS) score at days 0, 4, 7, 10, 14, 21, 28, 42 on PP data set in an observation carried (OC) approach. Secondary efficacy variables were clinical global impression (global improvement) and Hamilton depression rating scale (HDRS). RESULTS: Improvement in MADRS total score was greater in the pindolol group than in the placebo group from day 7 (p=0.03). Responder rates in the clinical global impression were 97.2% for the pindolol group and 60.6% for the placebo group. The treatment was well tolerated with the most common side effects being nausea (28.2%; 35.9%), vomiting (7.7%; 23.1%), hot flushes (15.4%; 5.1%) and sweating (12.8%; 12.8%). CONCLUSION: The milnacipran and pindolol combination is safe, well tolerated and efficacious in major depression, and represents a rational strategy for the possible acceleration or potentiation of antidepressant action.


Subject(s)
Antidepressive Agents/therapeutic use , Cyclopropanes/therapeutic use , Depressive Disorder/drug therapy , Pindolol/therapeutic use , Adolescent , Adult , Aged , Antidepressive Agents/administration & dosage , Antidepressive Agents/adverse effects , Cyclopropanes/administration & dosage , Cyclopropanes/adverse effects , Double-Blind Method , Drug Administration Schedule , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Milnacipran , Pindolol/administration & dosage , Pindolol/adverse effects , Psychiatric Status Rating Scales
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