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1.
Clin Infect Dis ; 65(4): 595-603, 2017 08 15.
Artículo en Inglés | MEDLINE | ID: mdl-28430880

RESUMEN

Background: Cerebral abscess is a recognized complication of pulmonary arteriovenous malformations (PAVMs) that allow systemic venous blood to bypass the pulmonary capillary bed through anatomic right-to-left shunts. Broader implications and mechanisms remain poorly explored. Methods: Between June 2005 and December 2016, at a single institution, 445 consecutive adult patients with computed tomography-confirmed PAVMs (including 403 [90.5%] with hereditary hemorrhagic telangiectasia) were recruited to a prospective series. Multivariate logistic regression was performed and detailed periabscess histories were evaluated to identify potential associations with cerebral abscess. Rates were compared to an earlier nonoverlapping series. Results: Thirty-seven of the 445 (8.3%) patients experienced a cerebral abscess at a median age of 50 years (range, 19-76 years). The rate adjusted for ascertainment bias was 27 of 435 (6.2%). Twenty-nine of 37 (78.4%) patients with abscess had no PAVM diagnosis prior to their abscess, a rate unchanged from earlier UK series. Twenty-one of 37 (56.7%) suffered residual neurological deficits (most commonly memory/cognition impairment), hemiparesis, and visual defects. Isolation of periodontal microbes, and precipitating dental and other interventional events, emphasized potential sources of endovascular inoculations. In multivariate logistic regression, cerebral abscess was associated with low oxygen saturation (indicating greater right-to-left shunting); higher transferrin iron saturation index; intravenous iron use for anemia (adjusted odds ratio, 5.4 [95% confidence interval, 1.4-21.1]); male sex; and venous thromboemboli. There were no relationships with anatomic attributes of PAVMs, or red cell indices often increased due to secondary polycythemia. Conclusions: Greater appreciation of the risk of cerebral abscess in undiagnosed PAVMs is required. Lower oxygen saturation and intravenous iron may be modifiable risk factors.


Asunto(s)
Malformaciones Arteriovenosas , Bacteriemia , Absceso Encefálico , Hipoxia , Telangiectasia Hemorrágica Hereditaria , Adulto , Anciano , Malformaciones Arteriovenosas/complicaciones , Malformaciones Arteriovenosas/epidemiología , Malformaciones Arteriovenosas/microbiología , Malformaciones Arteriovenosas/fisiopatología , Bacteriemia/complicaciones , Bacteriemia/epidemiología , Bacteriemia/microbiología , Bacteriemia/fisiopatología , Absceso Encefálico/complicaciones , Absceso Encefálico/epidemiología , Absceso Encefálico/microbiología , Absceso Encefálico/fisiopatología , Femenino , Humanos , Hipoxia/complicaciones , Hipoxia/epidemiología , Hipoxia/microbiología , Hipoxia/fisiopatología , Masculino , Persona de Mediana Edad , Morbilidad , Estudios Prospectivos , Arteria Pulmonar/anomalías , Venas Pulmonares/anomalías , Telangiectasia Hemorrágica Hereditaria/complicaciones , Telangiectasia Hemorrágica Hereditaria/epidemiología , Telangiectasia Hemorrágica Hereditaria/microbiología , Telangiectasia Hemorrágica Hereditaria/fisiopatología , Adulto Joven
2.
PLoS One ; 15(12): e0244709, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33382793

RESUMEN

BACKGROUND: When detected early, inexpensive measures can slow chronic kidney disease progression to kidney failure which, for children, confers significant morbidity and impacts growth and development. Our objective was to determine the incidence of late presentation of childhood chronic kidney disease and its associated risk factors. METHODS: We searched MEDLINE, Embase, PubMed, Web of Science, Cochrane Library and CINAHL, grey literature and registry websites for observational data describing children <21 years presenting to nephrology services, with reference to late presentation (or synonyms thereof). Independent second review of eligibility, data extraction, and risk of bias was undertaken. Meta-analysis was used to generate pooled proportions for late presentation by definition and investigate risk factors. Meta-regression was undertaken to explore heterogeneity. RESULTS: Forty-five sources containing data from 30 countries were included, comprising 19,339 children. Most studies (37, n = 15,772) described children first presenting in kidney failure as a proportion of the chronic kidney disease population (mean proportion 0.43, 95% CI 0.34-0.54). Using this definition, the median incidence was 2.1 (IQR 0.9-3.9) per million age-related population. Risk associations included non-congenital disease and older age. Studies of hospitalised patients, or from low- or middle-income countries, that had older study populations than high-income countries, had higher proportions of late presentation. CONCLUSIONS: Late presentation is a global problem among children with chronic kidney disease, with higher proportions seen in studies of hospitalised children or from low/middle-income countries. Children presenting late are older and more likely to have non-congenital kidney disease than timely presenting children. A consensus definition is important to further our understanding and local populations should identify modifiable barriers beyond age and disease to improve access to care.


Asunto(s)
Insuficiencia Renal Crónica/diagnóstico , Factores de Edad , Niño , Diagnóstico Tardío , Humanos , Factores de Riesgo
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