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1.
Br J Cancer ; 122(12): 1760-1768, 2020 06.
Article in English | MEDLINE | ID: mdl-32350413

ABSTRACT

BACKGROUND: Nab-paclitaxel plus gemcitabine (nabP+gemcitabine) offers modest survival gains for patients with metastatic pancreatic ductal adenocarcinoma (PDAC). Sequential scheduling of nabP+gemcitabine in a PDAC mouse model improved efficacy; this hypothesis was tested in a clinical trial. METHODS: Patients with previously untreated metastatic PDAC were randomised to receive nabP+gemcitabine administered either concomitantly on the same day, or sequentially, with gemcitabine administered 24 h after nabP. The primary outcome measure was progression-free survival (PFS). Secondary outcome measures were objective response rate (ORR), overall survival (OS), safety, quality of life (QoL) and predictive biomarkers. RESULTS: In total, 71 patients received sequential (SEQ) and 75 concomitant (CON) treatment. Six-month PFS was 46% with SEQ and 32% with CON scheduling. Median PFS (5.6 versus 4.0 months, hazard ratio [HR] 0.67, 95% confidence interval [95% CI] 0.47-0.95, p = 0.022) and ORR (52% versus 31%, p = 0.023) favoured the SEQ arm; median OS was 10.2 versus 8.2 months (HR 0.93, 95% CI 0.65-1.33, p = 0.70). CTCAE Grade ≥3 neutropaenia incidence doubled with SEQ therapy but was not detrimental to QoL. Strongly positive tumour epithelial cytidine deaminase (CDA) expression favoured benefit from SEQ therapy (PFS HR 0.31, 95% CI 0.13-0.70). CONCLUSIONS: SEQ delivery of nabP+gemcitabine improved PFS and ORR, with manageable toxicity, but did not significantly improve OS. CLINICAL TRIAL REGISTRATION: ISRCTN71070888; ClinialTrials.gov (NCT03529175).


Subject(s)
Albumins/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Carcinoma, Pancreatic Ductal/drug therapy , Deoxycytidine/analogs & derivatives , Paclitaxel/administration & dosage , Pancreatic Neoplasms/drug therapy , Aged , Aged, 80 and over , Carcinoma, Pancreatic Ductal/mortality , Deoxycytidine/administration & dosage , Drug Administration Schedule , Female , Humans , Male , Middle Aged , Pancreatic Neoplasms/mortality , Progression-Free Survival , Gemcitabine , Pancreatic Neoplasms
2.
J Public Health (Oxf) ; 40(4): 813-819, 2018 12 01.
Article in English | MEDLINE | ID: mdl-29385489

ABSTRACT

Background: Local authorities (LAs) have statutory responsibility to reduce health inequalities and improve public health. Place-based approaches may positively influence service provision yet little is known about their implementation and potential for reducing inequality through health and wellbeing improvements. An English LA implemented a place-based working (PBW) pilot in a small geography during austerity measures in the north of England. This involved three strands (early intervention, estate services and community intelligence) which were introduced separately and covered overlapping geographies. Predominantly focusing on early intervention, this qualitative study investigates stakeholders' perceptions of the pilot and its potential to improve health and wellbeing by reducing inequality. Methods: In total, 15 face-to-face qualitative interviews with stakeholders were completed. Thematic analysis produced context, mechanism and outcome configurations in a process adapted from realist evaluation methodology. Results: Stakeholders described PBW as holistic, upstream and cutting across departmental boundaries to engage staff and the community. Collaborative working was considered important and was aided by PBW in our study. Conclusions: PBW has the potential to reduce health inequalities by improving health and wellbeing. LAs deliver services that affect health and wellbeing and PBW may help develop a more coordinated response to improve outcomes and potentially save money.


Subject(s)
Health Status Disparities , Public Health Practice , Community Health Services/methods , Community Health Services/organization & administration , Community Participation/methods , England , Humans , Interviews as Topic , Local Government , Program Development , Qualitative Research
3.
Braz J Med Biol Res ; 52(2): e8130, 2019 Jan 24.
Article in English | MEDLINE | ID: mdl-30698228

ABSTRACT

Exposure to air pollution is an important cause of hospital admissions due to respiratory diseases. Nevertheless, few studies use pollutant concentration data estimated by mathematical models. A time-series ecological study was developed, using data from hospitalizations due to respiratory diseases in people over 60 years of age, residents of Cuiabá, Brazil, during 2012, obtained from the Brazilian Ministry of Health. The independent variables were the concentrations of fine particulate matter (PM2.5) and carbon monoxide (CO) estimated by mathematical modeling, minimum temperature, and relative humidity (obtained from the Brazilian Meteorological Agency), and the number of forest fires. The generalized linear regression model of Poisson was used, with lags of 0 to 7 days. The coefficients obtained were transformed into relative risk of hospitalization, with respective 95% confidence intervals; alpha=5% was adopted. In that year, 591 hospitalizations were evaluated, with a daily average of 1.61 (SD=1.49), the PM2.5 average concentration was 15.7 µg/m3, and the CO average concentration was 144.2 ppb. Significant associations between exposure to these contaminants and hospitalizations in lags 3 and 4 in 2012 were observed. There was a hospitalization risk increase of 31.8%, with an increase of 3.5 µg/m3 of PM2.5 concentrations and an increase of 188 in the total number of hospitalizations, with an expense of more than ≈US$ 96,000 for the Brazilian Public Health System. This study provided information on the cost of air pollution to the health system and the feasibility of using a mathematical model to estimate environmental concentration of air pollutants.


Subject(s)
Air Pollution/adverse effects , Carbon Monoxide/adverse effects , Environmental Exposure/adverse effects , Particulate Matter/adverse effects , Respiration Disorders/etiology , Aged , Brazil , Hospitalization , Humans , Middle Aged , Models, Theoretical , Poisson Distribution , Risk Factors , Seasons , Time Factors
4.
BMC Rheumatol ; 2: 32, 2018.
Article in English | MEDLINE | ID: mdl-30886982

ABSTRACT

Although treat-to-target has revolutionised the outcomes of patients with rheumatoid arthritis (RA) there is emerging evidence that attaining the target of remission is insufficient to normalise patients' quality of life, and ameliorate the extra-articular impacts of RA. RA has a broad range of effects on patient's lives, with four key "extra-articular" impacts being pain, depression and anxiety, fatigue and rheumatoid cachexia. All of these are seen frequently; for example, studies have reported that 1 in 4 patients with RA have high-levels of fatigue. Commonly used drug treatments (including simple analgesics, non-steroidal anti-inflammatory drugs and anti-depressants) have, at most, only modest benefits and often cause adverse events. Psychological strategies and dynamic and aerobic exercise all reduce issues like pain and fatigue, although their effects are also only modest. The aetiologies of these extra-articular impacts are multifactorial, but share overlapping components. Consequently, patients are likely to benefit from management strategies that extend beyond the assessment and treatment of synovitis, and incorporate more broad-based, or "holistic", assessments of the extra-articular impacts of RA and their management, including non-pharmacological approaches. Innovative digital technologies (including tablet and smartphone "apps" that directly interface with hospital systems) are increasingly available that can directly capture patient-reported outcomes during and between clinic visits, and include them within electronic patient records. These are likely to play an important future role in delivering such approaches.

5.
Mol Biochem Parasitol ; 101(1-2): 13-21, 1999 Jun 25.
Article in English | MEDLINE | ID: mdl-10413039

ABSTRACT

A Fasciola hepatica cDNA clone of 994 bp was isolated from an adult worm cDNA expression library using a rabbit serum against the excretory-secretory antigens. The nucleotide sequence of the cDNA clone revealed the presence of an open reading frame of 572 bp which encoded a 22 kDa polypeptide (Fh22) showing putative EF-hand domains. This gene was expressed in Escherichia coli and the recombinant protein used for the production of specific antibodies. Immunoblotting studies using the anti-Fh22 serum showed the presence of a polypeptide of similar molecular mass in the excretory-secretory extract of the adult parasite. The recombinant Fh22 polypeptide showed calcium-dependent electrophoretic mobility (decreased with Ca2(+)-ions and increased with EGTA). The observed behaviour of recombinant Fh22 in gel filtration experiments also suggested calcium-induced conformational changes.


Subject(s)
Calcium-Binding Proteins/genetics , Calcium-Binding Proteins/metabolism , Cloning, Molecular , Fasciola hepatica/genetics , Genes, Helminth , Helminth Proteins , Amino Acid Sequence , Animals , Antigens, Helminth/chemistry , Blotting, Northern , Calcium/metabolism , Calcium-Binding Proteins/chemistry , Calcium-Binding Proteins/immunology , Chromatography, Gel , Electrophoresis, Polyacrylamide Gel , Escherichia coli/genetics , Escherichia coli/metabolism , Fasciola hepatica/chemistry , Humans , Immunoblotting , Molecular Sequence Data , Protein Conformation , Rabbits , Sequence Analysis, DNA
6.
Genet Couns ; 10(3): 233-43, 1999.
Article in English | MEDLINE | ID: mdl-10546094

ABSTRACT

Mixed gonadal dysgenesis (MGD) is an abnormality of sexual differentiation (ASD), which encompasses an heterogeneous group of different gonadal and phenotypic abnormalities. This study describes the main clinical features found in 16 patients with MGD, relating the clinical presentation with cytogenetic evaluation and histopathological findings. For purpose of this study, MGD was considered in those patients who fulfilled the following diagnostic criteria: 1) müllerian and/or wolfflan derivatives; 2) any of the following gonadal characteristics: a) bilateral intrabdominal or scrotal immature testicular tissue; b) intrabdominal or scrotal immature testicular tissue with contralateral streak gonad. Patients were selected from an ASD study which was carried out in Medical Genetic Unit of University of Zulia (UGM-LUZ), Maracaibo, Venezuela, from 1980 to 1997. The following information was extracted from the medical history at UGM-LUZ: age, gender which patient was reared, clinical presentation, cytogenetic evaluation, laparoscopic findings and gonadal biopsy. Sixteen patients fulfilled the diagnostic criteria and ranged in age from 1.2 to 39.4 years with an average of 12.65 years. Only 5 patients were reared as males. Twelve patients consulted for genital ambiguity. Chromosomal evaluation was as following: 8 patients with 45,X/46,XY mosaicism: 5 had a 46,XY normal male karyotype and the remaining patients: 46,XX; 46,XX/46,XY and 45,X/46,Xi(Xq) karyotypes, respectively. All patients showed müllerian derivatives and occasionally wolffian derivatives. Gonadal tumors were present in 2 patients. Molecular studies of genes that govern gonadal development are necessary for a better understanding of the wide heterogeneity present in MGD.


Subject(s)
Gonadal Dysgenesis, Mixed/diagnosis , Gonadal Dysgenesis, Mixed/genetics , Sex Chromosomes/genetics , Adolescent , Adult , Child , Child, Preschool , Diagnosis, Differential , Female , Gonadal Dysgenesis, Mixed/pathology , Gonadal Dysgenesis, Mixed/surgery , Humans , Infant , Karyotyping , Male , Mosaicism
7.
Invest Clin ; 38(3): 145-53, 1997 Sep.
Article in Spanish | MEDLINE | ID: mdl-9376420

ABSTRACT

Cystic Fibrosis (CF) is a severe and relatively common autosomic recessive disease caused by a variety of mutations in the CFTR gene. The most frequent mutation worldwide, consists of the deletion of the phenylalanine codon at position 508 (delta F508). Here we report the first cases of prenatal diagnosis of CF by DNA analysis in couples at risk in Venezuela. The study focused on the detection of delta F508 alleles analyzing DNA recovered directly from amniocytes or from their cultures, using the polymerase chain reaction (PCR) and polyacrylamide gel electrophoresis. Two of three fetuses resulted homozygotic for the delta F508 allele and the third one turned out to be a delta F508 carrier. This information sustained the genetic counseling of the couples and allowed them to take objective reproductive decisions, a direct consequence of the availability of gene analysis at the DNA level.


Subject(s)
Amniocentesis , Cystic Fibrosis Transmembrane Conductance Regulator/genetics , Cystic Fibrosis/diagnosis , DNA Mutational Analysis , Fetal Diseases/diagnosis , Sequence Deletion , Adult , Alleles , Codon/genetics , Cystic Fibrosis/embryology , Female , Humans , Male , Pregnancy
8.
Invest Clin ; 39(2): 97-116, 1998 Jun.
Article in Spanish | MEDLINE | ID: mdl-9707921

ABSTRACT

The Prenatal Diagnosis Program of the Medical Genetic Unit of University of Zulia has the following objectives: Identification of Genetic Risk Factors (GRF) in those couples who attend to the Prenatal Genetic Clinic, application of different prenatal diagnostic procedures (PDP), and providing adequate genetic counseling. The goal of this paper is to show preliminary results obtained between January 1993 and December 1996. Three hundred and twenty one pregnant women were analyzed by determining the GRF and taking into account the genetic clinical history. The GRF analyzed were: Advanced maternal age (AMA), congenital malformation history (CMH), previous child with chromosomic anomalies (PCCA), defects of neural tube history (DNTH), congenital heart disease history (CHDH), any parent carrier of chromosomic anomaly (PCA), habitual abortion (HA), abnormal fetal echography (AFE), altered maternal serum levels of alpha-feto-protein (AMSAFP) and OTHERS: exposure to teratogenic agents, history of Mendelian diseases, maternal systemic diseases and anxiety in the mother or in her partner. The PDP was designed according to the GRF, which included fetal echography (FE), fetal echocardiography (FEc), amniocentesis (AMN), chordocentesis (CCT) and AMSAFP. Results showed that 58.4% of the expectant mothers asked for counseling during the 2nd trimester, 70% of the total showed only one GRF, and AMA was the most frequent GRF found (40.3%), followed by PCCA, AFE, CHDH, HA, DNTH, PCA, and OTHERS in that order. The specific PDP applied to the identified GRF allowed a health evaluation of the fetus. The GRF identification gave the opportunity of establishing a Prenatal Diagnostic Program producing a response to the couple's needs and showed the utility of an integral and multidisciplinary management directed to any expecting mother in order to identify any high GRF.


Subject(s)
Hospitals, University/organization & administration , Prenatal Care/organization & administration , Prenatal Diagnosis , Abortion, Habitual/epidemiology , Abortion, Habitual/genetics , Biomarkers , Chromosome Aberrations/diagnosis , Chromosome Aberrations/embryology , Chromosome Aberrations/epidemiology , Chromosome Aberrations/genetics , Chromosome Disorders , Congenital Abnormalities/diagnosis , Congenital Abnormalities/embryology , Congenital Abnormalities/epidemiology , Female , Fetal Diseases/diagnosis , Fetal Diseases/epidemiology , Genetic Counseling , Genetic Diseases, Inborn/diagnosis , Genetic Diseases, Inborn/embryology , Genetic Diseases, Inborn/epidemiology , Hospital Departments , Hospitals, University/statistics & numerical data , Humans , Infant, Newborn , Male , Maternal Age , Pregnancy , Pregnancy, High-Risk , Prenatal Care/statistics & numerical data , Prenatal Diagnosis/methods , Prenatal Diagnosis/statistics & numerical data , Retrospective Studies , Risk Factors , Venezuela/epidemiology , alpha-Fetoproteins/analysis
9.
An Med Interna ; 9(10): 483-6, 1992 Oct.
Article in Spanish | MEDLINE | ID: mdl-1420759

ABSTRACT

Giant cell arteritis, temporal arteritis (TA), is a vasculitis which affects large and medium-sized vessels. The von Willebrand factor (vWF) is synthesized by endothelial cells and megakaryocytes. Increased amounts of vWF are released into plasma in response to an endothelial damage. vWF levels were studied by Electro-Immunodiffusion in 16 patients with TA (8 of them with a positive biopsy) and their values were compared with 5 patients with Polymyalgia Rheumatica (PMR) and 32 controls. We found higher amount of vWF in global TA, biopsy-positive TA, biopsy-negative TA, and PMR than in controls. There were no relationship between vWF amounts in plasma and clinical findings nor the laboratory parameters. We feel that although in our study vWF might be of some help as an alternative to the biopsy in those patients with high suspicion of TA, the results of other authors raise doubt about the usefulness of the determination of vWF in TA.


Subject(s)
Giant Cell Arteritis/blood , von Willebrand Factor/analysis , Biopsy , Giant Cell Arteritis/pathology , Humans , Polymyalgia Rheumatica/blood
10.
Br J Community Nurs ; 5(2): 87-90, 2000 Feb.
Article in English | MEDLINE | ID: mdl-11125458

ABSTRACT

The children's disability team in Cambridge provides an integrated health and social care service for children with complex learning and physical disabilities and their families. The team uses a multidisciplinary and multi-agency teamwork approach to care provision. The effectiveness of the team was evaluated using a cooperative review of its functions, in which all the 'subjects' were active participants in defining and delivering the evaluation. This was combined with individual questionnaires regarding the team's perceived strengths and weaknesses. Particular implications for training and supervision emerged from the findings. This article discusses the ways in which the team has successfully refined its practice of collaborative working in a developmental way between 1992-1998.


Subject(s)
Community Health Nursing/organization & administration , Disabled Children/rehabilitation , Interprofessional Relations , Patient Care Team/organization & administration , Social Work/organization & administration , Child , Humans , Quality of Health Care , United Kingdom
11.
Anesteziol Reanimatol ; (1): 5-8, 1992.
Article in Russian | MEDLINE | ID: mdl-1524254

ABSTRACT

Intraoperative hemodynamics has been studied during orthotopic heart transplantation (OHT) in 36 recipients, aged 14 to 56 years, with spontaneous contractions of the graft. It has been established that patients with HR greater than 110 beats per min were in most cases characterized by normal central venous pressure (CVP) and venous blood oxygenation parameters. In lower HR, CVP is considerably higher and the indexes characteristic of the adequacy of cardiac output to body oxygen requirements are deteriorated. Right after OHT there is a reverse dependence between HR and CVP, with the lowest CVP values corresponding to HR intervals 101-120 and 121-140 per min. It has been concluded that tachycardia in the intraoperative period ensures a more effective function of the transplanted heart.


Subject(s)
Heart Rate/physiology , Heart Transplantation/physiology , Hemodynamics/physiology , Adolescent , Adult , Female , Humans , Intraoperative Period , Male , Middle Aged
12.
Braz. j. med. biol. res ; 52(2): e8130, 2019. tab, graf
Article in English | LILACS | ID: biblio-984026

ABSTRACT

Exposure to air pollution is an important cause of hospital admissions due to respiratory diseases. Nevertheless, few studies use pollutant concentration data estimated by mathematical models. A time-series ecological study was developed, using data from hospitalizations due to respiratory diseases in people over 60 years of age, residents of Cuiabá, Brazil, during 2012, obtained from the Brazilian Ministry of Health. The independent variables were the concentrations of fine particulate matter (PM2.5) and carbon monoxide (CO) estimated by mathematical modeling, minimum temperature, and relative humidity (obtained from the Brazilian Meteorological Agency), and the number of forest fires. The generalized linear regression model of Poisson was used, with lags of 0 to 7 days. The coefficients obtained were transformed into relative risk of hospitalization, with respective 95% confidence intervals; alpha=5% was adopted. In that year, 591 hospitalizations were evaluated, with a daily average of 1.61 (SD=1.49), the PM2.5 average concentration was 15.7 µg/m3, and the CO average concentration was 144.2 ppb. Significant associations between exposure to these contaminants and hospitalizations in lags 3 and 4 in 2012 were observed. There was a hospitalization risk increase of 31.8%, with an increase of 3.5 µg/m3 of PM2.5 concentrations and an increase of 188 in the total number of hospitalizations, with an expense of more than ≈US$ 96,000 for the Brazilian Public Health System. This study provided information on the cost of air pollution to the health system and the feasibility of using a mathematical model to estimate environmental concentration of air pollutants.


Subject(s)
Humans , Middle Aged , Aged , Respiration Disorders/etiology , Carbon Monoxide/adverse effects , Air Pollution/adverse effects , Environmental Exposure/adverse effects , Particulate Matter/adverse effects , Seasons , Time Factors , Brazil , Poisson Distribution , Risk Factors , Hospitalization , Models, Theoretical
13.
Leukemia ; 27(4): 925-31, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23174883

ABSTRACT

Currently, multiple myeloma (MM) patients are broadly grouped into a non-hyperdiploid (nh-MM) group, highly enriched for IgH translocations, or into a hyperdiploid (h-MM) group, which is typically characterized by trisomies of some odd-numbered chromosomes. We compared the micro RNA (miRNA) expression profiles of these two groups and we identified 16 miRNAs that were downregulated in the h-MM group, relative to the nh-MM group. We found that target genes of the most differentially expressed miRNAs are directly involved in the pathogenesis of MM; specifically, the inhibition of hsa-miR-425, hsa-miR-152 and hsa-miR-24, which are all downregulated in h-MM, leads to the overexpression of CCND1, TACC3, MAFB, FGFR3 and MYC, which are the also the oncogenes upregulated by the most frequent IgH chromosomal translocations occurring in nh-MM. Importantly, we showed that the downregulation of these specific miRNAs and the upregulation of their targets also occur simultaneously in primary cases of h-MM. These data provide further evidence on the unifying role of cyclin D pathways deregulation as the key mechanism involved in the development of both groups of MM. Finally, they establish the importance of miRNA deregulation in the context of MM, thereby opening up the potential for future therapeutic approaches based on this molecular mechanism.


Subject(s)
Diploidy , Down-Regulation , Immunoglobulin Heavy Chains/genetics , MicroRNAs/genetics , Multiple Myeloma/genetics , Translocation, Genetic , Base Sequence , Blotting, Western , DNA Methylation , DNA Primers , Humans , Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction
15.
Int J Parasitol ; 41(12): 1301-9, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21924271

ABSTRACT

Contrasting host and parasite population genetic structures can provide information about the population ecology of each species and the potential for local adaptation. Here, we examined the population genetic structure of the nematode Neoheligmonella granjoni at a regional scale in southeastern Senegal, using 11 microsatellite markers. Using the results previously obtained for the two main rodent species of the host community, Mastomys natalensis and Mastomys erythroleucus, we tested the hypothesis that the parasite population structure was mediated by dispersal levels of the most vagile host. The results showed similar genetic diversity levels between host and parasite populations, and consistently lower levels of genetic differentiation in N. granjoni, with the exception of one outlying locus with a high F(ST). The aberrant pattern at this locus was primarily due to two alleles occurring at markedly different frequencies in one locality, suggesting selection at this locus, or a closely linked one. Genetic differentiation levels and isolation by distance analyses suggested that gene flow was high and random in N. granjoni at the spatial scale examined. The correlation between pair-wise genetic differentiation levels in the parasite and its main host was consistent with the hypothesis tested. Models of local adaptation as a function of the dispersal rates of hosts and parasites suggest that opportunities for local adaptation would be low in this biological system.


Subject(s)
Genetic Variation , Murinae/parasitology , Rodent Diseases/parasitology , Trichostrongyloidea/classification , Trichostrongyloidea/isolation & purification , Trichostrongyloidiasis/veterinary , Animals , Gene Flow , Genetics, Population , Microsatellite Repeats , Senegal , Trichostrongyloidea/genetics , Trichostrongyloidiasis/parasitology
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