Trauma scoring in patients submitted to laparotomy

BACKGROUND: Trauma is a public health problem of vast proportions. It is the leading cause of death among young people. The Major Trauma Outcome Study (MTOS) is a retrospective descriptive study of injury severity and outcome, considered the largest database of descriptive contemporary injuries information. The objective of this paper is to compare the retrospective calculation of NISS with prospectively calculated ISS, using TRISS and a simple modification called NTRISS (New Trauma and Injury Severity Score), and to compare this population submitted to laparotomy with MTOS patients. METHODS: We studied 1.380 trauma adult patients submitted to laparotomy at Discipline of Trauma Surgery - Unicamp, in Campinas, during a 8-year period. Submitted data included: demographics, cause of injury (blunt or penetrating, gunshot or stab wounds), physiologic status at admission (RTS), anatomic injury diagnoses (ATI, ISS and NISS), survival probability using the TRISS and NTRISS, and patient outcomes (survival or death). Z statistic and W statistic, first described by Flora, were used to compare the predicted number of deaths (or survivors) with the baseline MTOS norm. RESULTS: The majority of these patients was male (88.3%) with a mean age of 30.4 years. Gunshot wounds were the most frequent (641 cases - 46.4%) mechanism of trauma. Thirty one per cent had blunt injuries. The median ATI, ISS and NISS values were, respectively, 12.3, 17.6 and 22.1. The overall mortality rate was 16.8% and the patients with blunt trauma had the highest mortality rate (29.3%). NISS better separated survivors from nonsurvivors than ISS, with higher specificity of NTRISS. It was observed a significantly less survivors than expected from outcomes norms (Z -16.24 with TRISS and Z -9.40 with NTRISS). Ranges of W values for each patient set demonstrated a difference in the numbers of nonsurvivors of 7.89 more deaths per 100 patients treated than expected from the MTOS using TRISS, while this values were reduced to 5.14 using NTRISS. CONCLUSION: The methods used for survival probability calculation presented limitations, particularly in this population with predominance of penetrating trauma. The NISS, with its derived NTRISS, was the score that better predicted survival than ISS. The results obtained with TRISS and NTRISS were significantly worse than MTOS, but this process of monitoring trauma patients have been important to ensure continued provision of quality of care.OBJETIVO: O trauma é um problema de saúde pública de enormes proporções. Constitui-se na principal causa de óbitos na população jovem. O Major Trauma Outcome Study (MTOS) é um estudo descritivo e retrospectivo da gravidade das lesões e evolução dos pacientes, considerado como o maior arquivo contemporâneo de informações descritivas de traumatizados. O objetivo do presente estudo é comparar o cálculo retrospectivo do New Injury Severity Score (NISS) com o Injury Severity Score (ISS) já calculado prospectivamente, utilizando o Trauma and Injury Severity Score (TRISS) e uma simples modificação deste índice, denominado de NTRISS (New Trauma and Injury Severity Score), e também comparar esta população submetida à laparotomia com os pacientes do MTOS. MÉTODO: Foram estudados 1.380 pacientes adultos traumatizados e submetidos à laparotomia na Disciplina de Cirurgia do Trauma da Unicamp, em Campinas, durante um período de oito anos. Os dados avaliados foram: demográficos, causa do trauma (fechado ou penetrante, ferimento por projétil de arma de fogo ou arma branca), estado fisiológico na admissão (RTS), diagnóstico anatômico de lesões (ATI, ISS e NISS), probabilidade de sobrevida utilizando o TRISS e o NTRISS, e a evolução do paciente (sobrevivência ou óbito). Foram utilizadas as estatísticas Z e W, inicialmente descritas por Flora, a fim de comparar a predição de óbitos ou sobreviventes com o estudo controle (MTOS). RESULTADOS: A maioria dos pacientes (88,3%) era do sexo masculino e jovem (média de idade de 30,4 anos). O ferimento por projétil de arma de fogo foi o mecanismo de trauma mais freqüente, com 641 casos (46,4%). Quatrocentos e trinta pacientes (31,2%) sofreram trauma fechado. As médias do ATI, ISS e NISS foram, respectivamente, de 12,3, 17,6 e 22,1. A taxa global de mortalidade foi de 16,8% e os pacientes com trauma contuso tiveram a maior mortalidade (29,3%). O NISS identificou melhor os sobreviventes e óbitos se comparado ao ISS, obtendo-se uma maior especificidade com o NTRISS. Foi observado um número significativamente menor de sobreviventes do que o esperado pelo estudo basal, com Z -16,24 com o TRISS e Z -9,40 se aplicado o NTRISS. Variações no valor da estatística W para cada paciente mostraram uma diferença no número de óbitos equivalente a 7,89 mais casos de óbito do que o esperado pelo MTOS, por 100 pacientes tratados, ao se empregar o TRISS, enquanto que estes valores foram reduzidos para 5,14 utilizando-se o NTRISS. CONCLUSÕES: Os métodos utilizados para cálculo da probabilidade de sobrevivência apresentaram limitações, particularmente nesta população com predomínio dos traumas penetrantes. O NISS, com o seu derivado NTRISS, foi o escore que obteve uma melhor predição de sobrevivência se comparado com o ISS. Os resultados obtidos com o TRISS e NTRISS foram estatisticamente piores do que os do MTOS, porém este processo de monitorização destes pacientes traumatizados tem sido importante para assegurar uma condição continuada de controle de qualidade.29930

Immunohistochemical study of basement membrane collagen IV in uterine cervix carcinoma

CONTEXT: The integrity of basement membrane (BM) is damaged during the evolution of a benign or potentially malignant lesion into a malignant one, in which it may undergo several degrees of discontinuity as a necessary condition for the invasive process. Immunostaining for collagen IV, which is exclusively found in BM, has been used to evaluate its formation in neoplastic and benign lesions of several organs.OBJECTIVE: To investigate BM continuity pattern in squamous carcinoma in situ (CIS), microinvasive (MIC) and invasive (IC) squamous cell carcinoma of the uterine cervix, and to find out if BM expression could be useful in the diagnosis of early stromal invasion (MIC).DESIGN: Archival material between 1988 and 1993 was studied at the Pathological Anatomy Department - Unicamp.PROCEDURES: The selected cases, previously formalin fixed and paraffin embedded, were reviewed retrospectively by submitting them to immunohistochemical study via the avidin-biotin-peroxidase method using a monoclonal antibody anticollagen IV.RESULTS: In all, 17 cases of CIS, 16 of MIC and 21 of IC were evaluated. All IC cases showed evident BM discontinuity, either focal or diffuse. In the CIS group, a continuous BM pattern was predominant, being focally disrupted in only 2/17 cases (11.8%). The MIC group showed an intermediate pattern, but with a clear tendency to BM discontinuity in 10/16 cases (62.5%). Inflammatory infiltrate, a variable also studied, cannot be considered responsible for BM discontinuity, since there was no statistical correlation between them.CONCLUSION: We conclude that immunostaining for collagen IV may contribute to the diagnosis of stromal invasion by BM discontinuity.CONTEXTO: A integridade da membrana basal (MB) é destruída no processo de evolução de uma lesão benigna ou potencialmente maligna para uma lesão maligna, onde ela pode sofrer vários graus de descontinuidade, como condição necessária para o processo de invasão. A imunocoloração para colágeno IV, que é exclusivamente encontrado na MB, tem sido utilizada para avaliar sua formação em processos benignos e neoplásicos de vários órgãos. OBJETIVO: Investigar o padrão de continuidade da MB no carcinoma in situ (CIS), microinvasivo (CMI) e epidermóide (CE) do colo uterino. Além disso, pretendeu-se verificar em que medida estes padrões poderiam ser úteis no diagnóstico de invasão estromal inicial (CMI). TIPO DE ESTUDO: Foi estudado o material do arquivo de tecidos dos anos de 1988 a 1993 do Departamento de Anatomia Patológica da UNICAMP. PROCEDIMENTOS: Os tecidos eram fixados em formalina e incluídos em parafina e foram revistos retrospectivamente para serem submetidos à reação imuno-histoquímica pelo método da avidina-biotina-peroxidase, com o anticorpo monoclonal anti-colágeno IV. RESULTADOS: Ao todo, foram avaliados 17 casos de CIS, 16 de CMI e 21 de CE. Todos os casos de CE mostraram evidente descontinuidade da MB, quer focal ou difusa. No grupo dos CIS foi observado um padrão contínuo de MB, sendo focalmente lesado em apenas 2/17 casos (11,8%). O grupo dos CMI mostraram um padrão intermediário, com clara tendência à descontinuidade da MB em 10/16 casos (62,5%). O infiltrado inflamatório, variável também estudada, não pode ser responsabilizado pela descontinuidade da MB, já que não houve correlação estatística entre eles. CONCLUSÃO: A imunocoloração para colágeno IV pode contribuir no diagnóstico de invasão estromal, quando houver lesão da MB.1846185

Sonolência excessiva diurna e uso de hipnóticos em idosos

Background: Excessive daytime somnolence (EDS) and hypnotics therapeutic use increase with age. Methods: A group of 148 elderly residents of a continued-care institution was interviewed by means of a structured questionnaire and also the Epworth sleepiness scale (ESS), from december 11, 2000 to february 02, 2001. There were descriptive statistics and analyzed by means of Student's t-tests, analysis of variance (ANOVA), chi-square and Pearson's Test. Results: EDS was present in 24% of the elderly persons of the sample (ESS >; 11). There was no association among age and residence time with EDS (p = 0.10 and p = 0.37 respectively), gender and instruction grade with EDS (p = 0.30 and p = 0.27 respectively). EDS wasn't associated with both hypnotic therapeutic use (p = 0.62) and alternative habits to sleep better (p = 0.65). The married people showed a higher frequency of EDS (p < 0.01). It was also seen that, decreased levels of daily activity were more frequent in those people with EDS (p = 0.05). Conclusion: There was a high prevalence of EDS, hypnotic and alternative sleep habits usage, without significative associations.Introdução: A sonolência excessiva diurna (SED) e o uso de hipnóticos aumentam com a idade. Método: Foram entrevistados 148 idosos, com um questionário estruturado e a escala de sonolência Epworth (ESS), de 11/12/2000 a 2/2/2001. Usaram-se estatísticas descritivas e os testes t de Student, análise da variância, qui-quadrado e teste de Pearson. Resultados: Tinham SED 24% dos idosos (11 pontos ou mais na ESS). Não houve associação entre a idade e o tempo de residência com SED (p = 0,10 e p = 0,37, respectivamente), o gênero e o grau de instrução (p = 0,30 e p = 0,27). Não houve associação significativa entre ausência ou presença de SED e uso de hipnótico (p = 0,62) e uso de meios alternativos para dormir melhor (p = 0,65). SED foi mais freqüente entre os casados/amasiados (p < 0,01). Houve uma maior proporção de entrevistados que consideraram ter tido muito prejuízo no dia seguinte entre aqueles com SED (p = 0,05). Conclusão: Houve uma alta prevalência de SED, uso de hipnóticos e de meios alternativos para dormir melhor entre os idosos, sem associações significativas entre estas variáveis

Clinical and laboratory characterization of hypertensive Chagas' disease patients without evident heart failure

This study evaluated the characteristics of 125 Chagas disease patients aged > 25 years or over who were attended at the Clinical Hospital of the State University of Campinas, State of São Paulo. Arterial pressure, age, gender, skin color, heart disease, body mass index, lipid profile, blood glucose level, alcohol and tobacco dependence, dyslipidemia, diabetes, anxiety disorders and obesity were investigated. It was found that the hypertensive Chagas disease patients were older than the non-hypertensive ones (p = 0.028). Among the hypertensive patients, there were more women (p = 0.015); higher blood glucose, LDL cholesterol and total cholesterol levels (p = 0.005, p = 0.024 and p = 0.017); more diabetics (p = 0.006); and more cardiac damage (p = 0.04) and left ventricular hypertrophy (p = 0.003). Only the age of patients with cardiac damage was shown to be higher (p = 0.003). The hypertensive Chagas disease patients presented clinical and laboratory characteristics that were similar to those of the general hypertensive population. This association may compound the harmful effects on the cardiovascular system.Este estudo avaliou as características de 125 chagásicos, > 25 anos, atendidos no Hospital de Clínicas da Universidade Estadual de Campinas, SP, considerando-se: pressão arterial, idade, gênero, cor, cardiopatia, índice de massa corporal, perfil lipídico, glicemia, etilismo, tabagismo, dislipidemia, diabetes, distúrbio de ansiedade e obesidade. Apresentavam hipertensão arterial 69 (55,2%) pacientes. Verificou-se que os chagásicos hipertensos eram mais idosos que os não hipertensos (p = 0,028). Entre os hipertensos havia: mais mulheres (p = 0,015); níveis mais elevados de glicemia, LDL-colesterol e colesterol total (p = 0,005; p = 0,024; p = 0,017); mais diabéticos (p = 0,006), dano cardíaco (p = 0,04) e sobrecarga ventricular esquerda (p = 0,003). Apenas a idade mostrou-se mais elevada nos pacientes com dano cardíaco (p = 0,003). Os chagásicos hipertensos apresentaram características clínico-laboratoriais semelhantes à população hipertensa, em geral. Dessa associação pode haver somatória de efeitos deletérios para o aparelho cardiovascular.16316

Avaliação clínica, epidemiológica, laboratorial, histológica e ultrassonográfica de doadores de sangue anti-HCV EIA-2 positivos

Between 1992 and 1997, 790 blood donors with anti-HCV EIA-2 strongly reagent (relationship between the sample optical density/cut-off >; 3) detected at the blood bank serological screening, were evaluated in ambulatory environment. They were all negative for Chagas disease, syphilis, hepatitis B (HBsAg) and AIDS. Blood samples were collected at the first ambulatorial evaluation, for hemogram, biochemical tests and new serological tests for HCV (anti-HCV EIA-2). In blood samples of 226 repeatedly reagent anti-HCV EIA-2 blood donors, supplementary "immunoblot" test for HCV (RIBA-2) was used. In 209 donors, the presence of HCV-RNA was investigated by the PCR test. The abdominal ultrasonography was realized in 366 donors. In 269 patients liver biopsy was performed for the histopathological study. The follow-up of blood donors showed that 95.6% were repeatedly EIA-2 reagent, 94% were symptomless and denied any hepatitis history, with only 2% mentioning previous jaundice. In 47% of this population at least one risk factor has been detected for the HCV transmission, the use of intravenous drugs being the main one (27.8%). Blood transfusion was the second factor for HCV transmission (27.2%). Hepatomegaly was detected in 54% of the cases. Splenomegaly and signs of portal hypertension have seldom been found in the physical examination, indicating a low degree of hepatic compromising in HCV. Abdominal ultrasound showed alterations in 65% of the subjects, being the steatosis the most frequent (50%). In 83.5% of the donors submitted to the liver biopsy, the histopathological exam showed the presence of chronic hepatitis, usually classified as active (89%) with mild or moderate grade in most of the cases (99.5%). The histopathological exam of the liver was normal in 1.5% of blood donors. The RIBA-2 test and the HCV-RNA investigation by PCR were positive in respectively 91.6 and 75% of the anti-HCV EIA-2 reagent donors. The HCV-RNA research was positive in 82% of the RIBA-2 positive subjects, in 37.5% of the indeterminate RIBA-2 donors and in 9% of the negative RIBA-2 donors. Chronic hepatitis has also been observed in 50% of the histopathological exams of the anti-HCV EIA-2 reagent donors which were indeterminate RIBA-2. Among 18 blood donors with minimal changes histopathological exam 11 (61%) were HCV-RNA positive. Our blood donors anti-HCV reagent generally had clinical, laboratorial and histopathological features observed in patients with chronic HCV hepatitis and a high proportion could be identified in interviews and medical evaluation realized in blood blanks. Generally, these HCV infected donors are identified and discharged only by the serological tests results.Entre 1992 e 1997 foram avaliados, ambulatorialmente, 790 doadores de sangue com teste anti-HCV EIA-2 fortemente reagente (relação entre a densidade ótica da amostra / "cut-off" >; 3), que haviam sido detectados na triagem sorológica do banco de sangue. Todos eram negativos para doença de Chagas, sífilis, hepatite B (HBsAg) e AIDS. Amostras de sangue foram coletadas, na primeira consulta ambulatorial, para a realização de hemograma, exames bioquímicos e novos testes sorológicos para a HVC (anti-HCV EIA-2). Em 226 doadores anti-HCV EIA-2 repetidamente reagentes, realizou-se o teste suplementar de "immunoblot" para a HVC (RIBA-2). Em 209 doadores, pesquisou-se a presença do RNA do VHC pelo teste do PCR, através de exame automatizado (HCV-AMPLICOR, ROCHE). A ultra-sonografia abdominal foi realizada em 366 doadores e a biópsia hepática em 269 concordantes. Notou-se que 95,6% eram EIA-2 repetidamente reagentes, 94% eram assintomáticos e que apenas 2% referiram icterícia pregressa. Em 47% detectou-se, pelo menos, um fator de risco para a transmissão do VHC, sendo o uso de drogas E.V. o principal deles (27,8%). A transfusão de sangue foi o segundo fator na transmissão da HVC (27,2%). Hepatomegalia foi encontrada em 54%. Esplenomegalia e sinais de hipertensão portal foram raramente encontrados no exame físico, denotando o baixo grau de comprometimento hepático na HVC. A ultra-sonografia abdominal mostrou-se alterada em 65% dos indivíduos, sendo a esteatose a alteração mais freqüentemente observada (50%). Em 83,5% dos doadores submetidos à biópsia hepática, diagnosticou-se hepatite crônica, geralmente classificada como ativa (89%) e de grau leve ou moderado na maioria dos casos (99,5%). O histopatológico foi normal em 1,5% dos doadores. O teste de RIBA-2 e a pesquisa do RNA do VHC pelo PCR foram positivos em, respectivamente, 91,6 e 75% dos doadores anti-HCV EIA-2 reagentes. A pesquisa do RNA do VHC foi positiva em 82% dos indivíduos RIBA-2 reagentes, em 37,5% dos doadores RIBA-2 indeterminados e em 9% dos RIBA-2 negativos. Hepatite crônica foi observada em 50% dos doadores RIBA-2 indeterminados. Entre 18 doadores com alterações mínimas, ao exame histopatológico, 11 (61%) eram positivos para o RNA do VHC. Nossos doadores de sangue anti-HCV reagentes geralmente apresentam alterações clínicas, laboratoriais e histopatológicas próprias de pacientes com hepatites crônicas pelo VHC e uma elevada proporção destes podem ser identificados em entrevistas e avaliação médicas rotineiramente realizadas em bancos de sangue. Geralmente estes doadores infectados pelo VHC somente são identificados e bloqueados pelos resultados dos testes sorológicos

Risk factors on the treatment of cecum injuries with primary suture in rats

Purpose: Analyze the results of primary suture in the treatment of cecum traumatic injuries in rats, after the exposure to increasing time intervals between the trauma and the surgery and with different peritonitis degrees. Methods: In a randomized double-blinded study, 96 Wistar male rats, weight ranging between 200 and 250 grams, underwent laparotomy, in which a 5-milimiter-diameter-injury in the contramesenteric edge of the cecum was performed. In 12 animals of the control-group a prompt primary suture was executed, with total and separated stitches, with 7.0 polypropylene thread. In the other groups, with 12 animals each, a laparotomy for repair of the injury was executed after intervals of 30 minutes, 1, 2, 4, 6, 9 and 12 hours. At the time of injury repair, one of its edges was ressected and sent for anatomopathological examination. A daily control after the surgery was done, observing the presence of complications, specially dehiscence of the suture, and the euthanasia of the animals were done in the 1st, 4th, 7th and 14th day after the surgery. Necropsy was executed in all animals, observing the macroscopic and microscopic findings in the area of suture. Results: There was no association between the delay for surgical treatment of the injury and peritonitis degrees. The mortality in the 14 animals with diffuse peritonitis was 100%. Global mortality was 25% (24 animals), and 6 animals (25%) died before treatment. None of the animals treated that evolved to death had complications related to the suture of the injury. These early deaths were due to peritonitis and sepsis. Among the 72 surviving rats, there was dehiscence of the suture in 9 animals (12.5%). This complication was statistically significant greater in animals operated on after the sixth hour following the trauma. The incidence of dehiscence was also greater in the rats presenting more intense fecal contamination. Intensity of the peritonitis at the moment of suture observed in histological examination had no association with the occurrence of complications of the primary suture. Conclusion: The primary suture as a risky procedure to treat rats, after an interval superior to six hours after the trauma or in the period of intense contamination of the cavity by feces.Objetivo: O presente trabalho teve como objetivo avaliar os resultados da sutura primária no tratamento das lesões traumáticas de ceco em ratos, após exposição a intervalos de tempo crescentes entre o trauma e a cirurgia, e com diferentes graus de peritonite. Métodos: Em estudo randomizado, duplo-cego, 96 ratos Wistar, machos, com peso variando de 200 a 250 gramas, foram submetidos a laparotomia, em que se realizava lesão de 5 milímetros de diâmetro na borda contramesentérica do ceco. Em 12 animais do grupo-controle realizava-se de imediato sutura primária com pontos totais, separados, com fio de polipropileno 7.0. Nos demais grupos, com 12 animais cada, a laparotomia para reparo da lesão foi realizada após intervalos de: 30 minutos, 1, 2, 4, 6, 9 e 12 horas. No momento do reparo da lesão, uma das suas bordas era ressecada e enviada para exame anatomopatológico. Foi feito controle diário no pós-operatório, atentando-se para a presença de complicações, em especial deiscência da sutura, sendo a eutanásia dos animais realizada no 1º, 4º, 7º e 14º dia de pós-operatório. Em todos animais foi realizada necropsia, atentando-se aos achados macroscópicos e microscópicos do local da sutura. Resultados: Não houve associação entre a demora para o tratamento cirúrgico da lesão e a evolução para graus mais avançados de peritonite. A mortalidade nos 14 animais com peritonite difusa foi de 100%. A mortalidade global foi de 25% (24 animais), sendo que 6 animais (25% dos óbitos) morreram antes do tratamento. Nenhum dos animais tratados que evoluíram a óbito teve complicação relacionada com a sutura da lesão. Os óbitos foram precoces, decorrentes de peritonite e sepse. Entre os 72 ratos sobreviventes, observou-se deiscência da sutura em 9 animais (12,5%). A ocorrência desta complicação foi maior em animais operados a partir da sexta hora após o trauma, sendo os resultados estatisticamente significativos. A incidência de deiscência também foi maior nos ratos que apresentavam contaminação fecal mais intensa da cavidade peritoneal. A intensidade da peritonite no momento da sutura observada no exame histológico não teve associação com a ocorrência de complicações da sutura primária. Conclusão: A sutura primária é um procedimento de risco para tratar ratos, transcorrido intervalo superior a seis horas após o trauma, ou na vigência de contaminação intensa da cavidade por fezes.61762

Patient-physician discordance in assessment of adherence to inhaled controller medication: a cross-sectional analysis of two cohorts

We aimed to compare patient's and physician's ratings of inhaled medication adherence and to identify predictors of patient-physician discordance.(SFRH/BPD/115169/2016) funded by Fundação para a Ciência e Tecnologia (FCT); ERDF (European Regional Development Fund) through the operations: POCI-01-0145-FEDER-029130 ('mINSPIRERS—mHealth to measure and improve adherence to medication in chronic obstructive respiratory diseases—generalisation and evaluation of gamification, peer support and advanced image processing technologies') cofunded by the COMPETE2020 (Programa Operacional Competitividade e Internacionalização), Portugal 2020 and by Portuguese Funds through FCT (Fundação para a Ciência e a Tecnologia).info:eu-repo/semantics/publishedVersio

Morphological and Postural changes in the foot during pregnancy and puerperium : a longitudinal study

The aim of this study is to observe the morphological and postural changes to the foot that take place during pregnancy and the puerperium. Method: In this descriptive, observational, longitudinal study, we analysed 23 pregnant women, with particular attention to morphological and postural aspects of the foot, at three time points during and after pregnancy: in weeks 9-13 of gestation, weeks 32-35 of gestation and weeks 4-6 after delivery. The parameters considered were changes in foot length, the Foot Posture Index (FPI) and the Hernández Corvo Index, which were analysed using a pedigraph and taking into account the Body Mass Index (BMI). The same procedure was conducted in each review. Results: The statistical analyses obtained for each foot did not differ significantly between the three measurement times. A pronator-type footprint was most frequently observed during the third trimester of pregnancy; it was predominantly neutral during the postpartum period. Statistically significant differences between the measurement times were obtained in the right foot for cavus vs. neutral foot type (between the first and third trimesters and also between the first trimester and the puerperium) (in both cases, p < 0.0001). Conclusions: Foot length increases in the third trimester and returns to normal in the puerperium. According to FPI findings, the third trimester of pregnancy is characterised by pronation, while the posture returns to neutrality during the postpartum period. During pregnancy, the plantar arch flattens, and this persists during the puerperium. The incidence of cavus foot increases significantly in the third trimester and in the puerperium

Identification of clusters of asthma control: A preliminary analysis of the inspirers studies

This work was funded by ERDF (European Regional Development Fund) through the operations: POCI- -01-0145-FEDER-029130 (“mINSPIRERS—mHealth to measure and improve adherence to medication in chronic obstructive respiratory diseases - generalisation and evaluation of gamification, peer support and advanced image processing technologies”) co-funded by the COMPETE2020 (Programa Operacional Competitividade e Internacionalização), Portugal 2020 and by Portuguese Funds through FCT (Fundação para a Ciência e a Tecnologia).© 2020, Sociedade Portuguesa de Alergologia e Imunologia Clinica. All rights reserved. Aims: To identify distinct asthma control clusters based on Control of Allergic Rhinitis and Asthma Test (CARAT) and to compare patients’ characteristics among these clusters. Methods: Adults and adolescents (≥13 years) with persistent asthma were recruited at 29 Portuguese hospital outpatient clinics, in the context of two observational studies of the INSPIRERS project. Demographic and clinical characteristics, adherence to inhaled medication, beliefs about inhaled medication, anxiety and depression, quality of life, and asthma control (CARAT, >24 good control) were collected. Hierarchical cluster analysis was performed using CARAT total score (CARAT-T). Results: 410 patients (68% adults), with a median (percentile 25–percentile 75) age of 28 (16-46) years, were analysed. Three clusters were identified [mean CARAT-T (min-max)]: cluster 1 [27(24-30)], cluster 2 [19(14-23)] and cluster 3 [10(2-13)]. Patients in cluster 1 (34%) were characterised by better asthma control, better quality of life, higher inhaler adherence and use of a single inhaler. Patients in clusters 2 (50%) and 3 (16%) had uncontrolled asthma, lower inhaler adherence, more symptoms of anxiety and depression and more than half had at least one exacerbation in the previous year. Further-more, patients in cluster 3 were predominantly female, had more unscheduled medical visits and more anxiety symp-toms, perceived a higher necessity of their prescribed inhalers but also higher levels of concern about taking these inhalers. There were no differences in age, body mass index, lung function, smoking status, hospital admissions or specialist physician follow-up time among the three clusters. Conclusion: An unsupervised method based on CARAT--T, identified 3 clusters of patients with distinct, clinically meaningful characteristics. The cluster with better asthma control had a cut-off similar to the established in the validation study of CARAT and an additional cut-off seems to distinguish more severe disease. Further research is necessary to validate the asthma control clusters identified.publishersversionpublishe