RESUMO
After over a century, fingerprints are still one of the most powerful means of biometric identification. The conventional forensic workflow for suspect identification consists of (i) recovering latent marks from crime scenes using the appropriate enhancement technique and (ii) obtaining an image of the mark to compare either against known suspect prints and/or to search in a Fingerprint Database. The suspect is identified through matching the ridge pattern and local characteristics of the ridge pattern (minutiae). However successful, there are a number of scenarios in which this process may fail; they include the recovery of partial, distorted or smudged marks, poor quality of the image resulting from inadequacy of the enhancement technique applied, extensive scarring/abrasion of the fingertips or absence of suspect's fingerprint records in the database. In all of these instances it would be very desirable to have a technology able to provide additional information from a fingermark exploiting its endogenous and exogenous chemical content. This opportunity could potentially provide new investigative leads, especially when the fingermark comparison and match process fails. We have demonstrated that Matrix Assisted Laser Desorption Ionisation Mass Spectrometry and Mass Spectrometry Imaging (MALDI MSI) can provide multiple images of the same fingermark in one analysis simultaneous with additional intelligence. Here, a review on the pioneering use and development of MALDI MSI for the analysis of latent fingermarks is presented along with the latest achievements on the forensic intelligence retrievable.
Assuntos
Dermatoglifia , Ciências Forenses/métodos , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz/métodos , Ciências Forenses/tendências , Humanos , Preparações Farmacêuticas/análise , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz/tendênciasRESUMO
Matrix deposition is a crucial aspect for successful matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI MSI) analysis. The search for more efficient protocols over the years has resulted in the devising of "dry matrix methods" in which the matrix is solely or preliminarily deposited as powder and acts in most cases as a seeding agent. Although not fully embraced by the MALDI MSI community, these methods have proven to be more efficient in terms of ion intensity, ion abundance, and ion images in the experimental circumstances they were employed. Here we report a novel two-step matrix application method, that we have named the "dry-wet" method, where the matrix is dusted onto the sample followed by solvent spray using a robotic device. The new method has been successfully applied to the detection and mapping of several analyte classes within latent fingermarks. Dusting the matrix generated the added advantage of enhancing the latent fingermarks which are invisible. This allows not only for an optical image to be taken of the fingermark in situ but also bridges the gap in the application of MALDI MSI technology in this field; with the use of the methodology reported, fingermark enhancement, recovery, and analysis from different surfaces is now compatible with subsequent MALDI MSI analysis thus allowing visual and chemical information to be obtained simultaneously.
RESUMO
Prehospital analgesia is vital to good clinical care and inhaled methoxyflurane (Penthrox) would be a valuable addition to the armed forces medical armoury. Penthrox would provide strong, fast-acting, self-administered and safe analgesia to patients with moderate to severe injuries. In addition, it would provide an option for strong analgesia which would not be subject to the regulations that govern controlled or accountable drugs which gives it a unique position as the military moves its focus from large enduring operations to small short-term training teams supported by lone combat medics in remote locations across the globe.
Assuntos
Analgesia/normas , Serviços Médicos de Emergência/tendências , Metoxiflurano/farmacologia , Analgesia/métodos , Analgesia/tendências , Anestésicos Inalatórios/administração & dosagem , Anestésicos Inalatórios/farmacologia , Anestésicos Inalatórios/uso terapêutico , Serviços Médicos de Emergência/métodos , Humanos , Metoxiflurano/administração & dosagem , Metoxiflurano/uso terapêutico , Manejo da Dor/métodos , Manejo da Dor/normas , Manejo da Dor/estatística & dados numéricos , Medição da Dor/métodos , Reino UnidoRESUMO
The changing pattern of disease in the population of Addu Atoll, Republic of Maldives, Indian Ocean, is reviewed. Over 30 years the population has nearly trebled with an increasing percentage in those under the age of 15 years. Diarrhoeal diseases and respiratory infections are now the dominant health problems where previously malaria and filariasis were major causes of morbidity. These problems are discussed against a background of changing financial resources and standards of health care.
Assuntos
Morbidade , Adolescente , Criança , Pré-Escolar , Humanos , Ilhas do Oceano Índico , Lactente , Recém-Nascido , Fenômenos Fisiológicos da Nutrição , Crescimento DemográficoRESUMO
Of 209 patients with liver disease attending the Al Qassimi Hospital, Sharjah, 172 were suffering from acute hepatitis. The proportion harbouring the hepatitis B surface antigen was unknown. Of the remainder, 10 were suffering from chronic active hepatitis, five from primary hepatoma and six from cirrhosis. Infection with hepatitis virus B was regarded as of aetiological significance in three cases of chronic active hepatitis, four of primary hepatoma and two of cirrhosis.
Assuntos
Hepatopatias/epidemiologia , Adolescente , Adulto , Idoso , Carcinoma Hepatocelular/epidemiologia , Pré-Escolar , Feminino , Hepatite/epidemiologia , Antígenos de Superfície da Hepatite B/análise , Humanos , Cirrose Hepática/epidemiologia , Hepatopatias/imunologia , Hepatopatias/patologia , Hepatopatias Parasitárias/epidemiologia , Neoplasias Hepáticas/epidemiologia , Masculino , Pessoa de Meia-Idade , Emirados Árabes UnidosRESUMO
Latent fingermarks are impressions of the skin ridge pattern that are transferred by the accidental contact of fingertips with a deposition surface. The ability to enhance, lift and produce an image of a latent fingermark, for comparison and suspect match against a central fingerprint database, provides forensic investigators with what is still considered one of the most powerful means of biometric identification to date. Identification relies on the recovery, visualisation, extraction and comparison of local characteristics of the ridge pattern (minutiae) that are unique to individuals. Therefore, both for manual inspection of the minutiae and using automated ridge extraction algorithms, the clearer the ridge details, the more reliable and successful the match. Overlapping fingermarks pose a remarkable challenge in this context and are often encountered when developing marks from crime scenes. Here we propose the use of Matrix Assisted Laser Desorption Ionisation Mass Spectrometry Imaging (MALDI MSI) to separate overlapping fingermarks using ion signals that are characteristic of each fingermark and that may be endogenous or exogenous in nature. In this work we show that the methodology works in a number of different scenarios both using manual inspection of the spectrum profile or a much quicker multivariate statistical analysis.
Assuntos
Dermatoglifia , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Cafeína/análise , Estimulantes do Sistema Nervoso Central/análise , Humanos , Análise Multivariada , Sebo/química , Suor/químicaRESUMO
The current British Thoracic Society guidelines on COPD recommend that patients with COPD exacerbations should be admitted to hospital if they either have partial pressure of arterial oxygen of <7.0 kilopascals (kPa) or if they are living alone. This study was carried out to see if either of these factors have any effect on the outcome in patients presenting with COPD exacerbation in the setting of well established COPD services. This study was to see if patients with PaO2 < 7.0 kPa or those living alone were readmitted more frequently or had higher mortality than other patients discharged through the same scheme. A retrospective analysis was carried out on 1078 patients with acute exacerbation of COPD who were discharged home through Wigan "hospital at home" scheme in the period between November 1999 and February 2004 prior to the introduction of the new guidelines. This study found that there was no statistically significant difference in the rates of readmissions in patients with low PaO2 or those living in adverse social circumstances compared to other groups of patients. The number of patients dying in this period was too small to analyse with adequate power. This study indicates that such patients can be safely managed at home in the context of well established COPD services.
Assuntos
Serviços Hospitalares de Assistência Domiciliar , Avaliação de Resultados em Cuidados de Saúde , Oxigênio/sangue , Doença Pulmonar Obstrutiva Crônica/terapia , Apoio Social , Adulto , Cuidadores , Feminino , Humanos , Hipóxia/etiologia , Masculino , Readmissão do Paciente/estatística & dados numéricos , Doença Pulmonar Obstrutiva Crônica/sangue , Doença Pulmonar Obstrutiva Crônica/complicações , Resultado do Tratamento , Reino UnidoRESUMO
A whole population survey was performed in Addu Atoll, southern Maldives to establish the prevalence of bronchial asthma. Assessments of atopic eczema, allergic rhinitis, conjunctivitis and intestinal infection were made, and serum specific IgE titres to a number of allergens were measured. Asthma is a common condition in the southern Maldives, and there is no evidence that the IgE produced by intestinal helminths prevents the condition.
Assuntos
Asma/epidemiologia , Adolescente , Adulto , Idoso , Asma/complicações , Criança , Pré-Escolar , Conjuntivite/complicações , Eczema/complicações , Fezes/parasitologia , Feminino , Humanos , Hipersensibilidade Imediata/complicações , Imunoglobulina E , Ilhas do Oceano Índico , Lactente , Masculino , Pessoa de Meia-Idade , Rinite Alérgica Perene/complicações , Testes CutâneosRESUMO
In a randomized, double-blind, double-dummy, crossover study consisting of two 1-month periods with a 2-week 'run-in' we compared the effects of a combination of fenoterol with ipratropium bromide (Duovent, Boehringer Ingelheim) and salbutamol administered by standard metered dose inhalers in conventional dosage in young adults with nocturnal asthma. Seventeen patients were studied, all were aged between 19 and 35 years and showed 'morning dip' associated with nocturnal symptoms of cough, wheeze and breathlessness. They recorded morning and evening peak flows and symptoms of nocturnal asthma on diary cards. Over the 10 weeks of the study there was no difference between Duovent and salbutamol in any of the parameters measured.
Assuntos
Albuterol/uso terapêutico , Asma/tratamento farmacológico , Derivados da Atropina/administração & dosagem , Fenoterol/administração & dosagem , Ipratrópio/administração & dosagem , Administração por Inalação , Adulto , Albuterol/administração & dosagem , Ensaios Clínicos como Assunto , Método Duplo-Cego , Combinação de Medicamentos/administração & dosagem , Combinação de Medicamentos/uso terapêutico , Feminino , Fenoterol/uso terapêutico , Humanos , Ipratrópio/uso terapêutico , Masculino , Distribuição AleatóriaRESUMO
A 60-year-old man with seropositive rheumatoid arthritis developed rapidly progressive dyspnoea and bilateral pulmonary infiltrates on short exposure to 50 mg penicillamine daily. He made a satisfactory recovery following cessation of penicillamine therapy and the addition of prednisolone. This case has been reported to the Committee on Safety of Medicines and we would like to emphasize that the possibility of penicillamine-induced lung disease should be recognized, even on a small dose of short duration.
Assuntos
Artrite Reumatoide/tratamento farmacológico , Penicilamina/efeitos adversos , Fibrose Pulmonar/induzido quimicamente , Humanos , Masculino , Pessoa de Meia-Idade , Penicilamina/uso terapêutico , Prednisolona/uso terapêutico , Fibrose Pulmonar/diagnóstico por imagem , RadiografiaRESUMO
One hundred sixty-three patients with small cell lung cancer were treated with six courses, at 3-week intervals, of ifosfamide (5 g/m2) with mesna and etoposide. Thoracic radiotherapy was delivered to the limited stage (LS) patients. The complete response rate (CR, determined clinically and radiologically) was 76% for the 78 LS patients with a further 14% partial response (PR). The majority of the CRs were confirmed on a follow-up bronchoscopy. The CR rate was 27% for extensive stage (ES) patients with another 38% undergoing a partial response. The median survival for LS patients was 11 months, (16 months for CR confirmed by rebronchoscopy) and 8 months for ES patients. The 2-year actuarial survival for LS patients is 27%, follow-up ranges from 12 months to 30 months with a median of 22 months. Toxicity was not severe for the patient population, of whom only 20% had a good performance status before chemotherapy. Parental antibiotics were required on 4% of all 844 chemotherapy courses and 12% of courses were delayed due to side effects. The majority of responses occurred within the first two courses of chemotherapy and there was a corresponding improvement in the patients' symptoms and performance status. The regimen produced rapid tumor response with corresponding improvement in symptoms without marked toxicity and allowed further treatment development.
Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Carcinoma de Células Pequenas/tratamento farmacológico , Neoplasias Pulmonares/tratamento farmacológico , Adulto , Idoso , Protocolos de Quimioterapia Combinada Antineoplásica/efeitos adversos , Carcinoma de Células Pequenas/radioterapia , Terapia Combinada , Etoposídeo/administração & dosagem , Etoposídeo/efeitos adversos , Estudos de Avaliação como Assunto , Feminino , Humanos , Ifosfamida/administração & dosagem , Ifosfamida/efeitos adversos , Lorazepam/administração & dosagem , Neoplasias Pulmonares/radioterapia , Masculino , Mesna/administração & dosagem , Metoclopramida/administração & dosagem , Pessoa de Meia-IdadeRESUMO
OBJECTIVES: To examine the relation between rheumatoid arthritis (RA) and bronchiectasis (BR). METHODS: Disease activity, outcome, extra-articular manifestations, and laboratory features were compared in 32 patients with BR and RA (RA-BR group), 32 matched patients with RA without BR (RA group), and 31 patients with BR but without arthritis (BR group). RESULTS: In 30 of the 32 (94%) patients with RA-BR, BR preceded RA. There was no functional or radiological difference between the RA-BR and RA groups, and except for xerophthalmia, which was more common in patients with RA-BR than patients with RA, there was no difference in extra-articular or laboratory features. CONCLUSIONS: Bronchiectasis does not lead to a more aggressive disease course in RA and, despite the recognised association, BR is not an extra-articular manifestation of rheumatoid disease.
Assuntos
Artrite Reumatoide/complicações , Bronquiectasia/complicações , Adulto , Artrite Reumatoide/imunologia , Artrite Reumatoide/fisiopatologia , Autoanticorpos/análise , Bronquiectasia/imunologia , Bronquiectasia/fisiopatologia , Feminino , Pé/diagnóstico por imagem , Volume Expiratório Forçado , Mãos/diagnóstico por imagem , Humanos , Imunoglobulinas/análise , Masculino , Pessoa de Meia-Idade , Prognóstico , Radiografia , Capacidade VitalRESUMO
One hundred and three patients with small cell lung carcinoma were stratified according to stage of disease (47 limited disease, 56 extensive disease) and then randomised to receive etoposide 300 mg/m2 alone for two days or a combination (VAC) of vincristine 1 mg/m2, doxorubicin (Adriamycin) 50 mg/m2, and cyclophosphamide 1000 mg/m2. The drugs were given at three week intervals. Patients were assessed after three cycles of treatment and continued with the same regimen if in complete remission and with the alternative regimen if in partial remission; they were withdrawn if the disease had progressed. Twenty four patients (23%) achieved complete remission and this occurred more often when patients were receiving VAC (19 of 82) than etoposide (5 of 75). There was no difference, however, in overall survival between those initially treated with etoposide and those having combination chemotherapy, whether for limited disease (both 8 months) or extensive disease (7 and 5.5 months). Toxicity was less with etoposide. Survival was disappointing, especially with limited disease, even in patients who showed a complete response to treatment.
Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Carcinoma de Células Pequenas/tratamento farmacológico , Etoposídeo/uso terapêutico , Neoplasias Pulmonares/tratamento farmacológico , Análise Atuarial , Adulto , Idoso , Carcinoma de Células Pequenas/mortalidade , Ciclofosfamida/administração & dosagem , Doxorrubicina/administração & dosagem , Feminino , Humanos , Neoplasias Pulmonares/mortalidade , Masculino , Pessoa de Meia-Idade , Vincristina/administração & dosagemRESUMO
BACKGROUND: Despite current recommendations, many people with asthma do not receive annual vaccination against influenza, partly because of concern that vaccine may trigger exacerbations. Colds can trigger exacerbations, which may be mistaken for vaccine-related adverse events. We undertook a double-blind placebo-controlled multicentre crossover study to assess the safety of influenza vaccine in patients with asthma, with allowance for the occurrence of colds. METHODS: We studied 262 patients, aged 18-75 years, who recorded daily peak expiratory flow (PEF), respiratory symptoms, medication, medical consultations, and hospital admissions for 2 weeks before the first injection and until 2 weeks after the second injection. Order of injection (vaccine and placebo) was assigned randomly. There was an interval of 2 weeks between injections. The main outcome measure was an exacerbation of asthma within 72 h of injection (defined as a fall in PEF of >20%). FINDINGS: Among 255 participants with paired data, 11 recorded a fall in PEF of more than 20% after vaccine compared with three after placebo (McNemar's test p=0.06); a fall of more than 30% was recorded by eight after vaccine compared with none after placebo (binomial test p=0.008). However, when participants with colds were excluded, there was no significant difference in the numbers with falls of more than 20% between vaccine and placebo (six vs three; binomial test p=0.51), although the difference for PEF decreases of more than 30% approached significance (five vs none; binomial test, p=0.06). This association was confined to first-time vaccinees. INTERPRETATION: Our findings indicate that pulmonary-function abnormalities may occur as a complication of influenza vaccination. However, the risk of pulmonary complications is very small and outweighed by the benefits of vaccination.