Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
1.
AJNR Am J Neuroradiol ; 38(9): 1814-1819, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28729296

ABSTRACT

BACKGROUND AND PURPOSE: The early diagnosis of spinal vascular malformations suffers from the nonspecificity of their clinical and radiologic presentations. Spinal angiography requires a methodical approach to offer a high diagnostic yield. The prospect of false-negative studies is particularly distressing when addressing conditions with a narrow therapeutic window. The purpose of this study was to identify factors leading to missed findings or inadequate studies in patients with spinal vascular malformations. MATERIALS AND METHODS: The clinical records, laboratory findings, and imaging features of 18 patients with spinal arteriovenous fistulas and at least 1 prior angiogram read as normal were reviewed. The clinical status was evaluated before and after treatment by using the Aminoff-Logue Disability Scale. RESULTS: Eighteen patients with 19 lesions underwent a total of 30 negative spinal angiograms. The lesions included 9 epidural arteriovenous fistulas, 8 dural arteriovenous fistulas, and 2 perimedullary arteriovenous fistulas. Seventeen patients underwent endovascular (11) or surgical (6) treatment, with a delay ranging between 1 week and 32 months; the Aminoff-Logue score improved in 13 (76.5%). The following factors were identified as the causes of the inadequate results: 1) lesion angiographically documented but not identified (55.6%); 2) region of interest not documented (29.6%); or 3) level investigated but injection technically inadequate (14.8%). CONCLUSIONS: All the angiograms falsely reported as normal were caused by correctible, operator-dependent factors. The nonrecognition of documented lesions was the most common cause of error. The potential for false-negative studies should be reduced by the adoption of rigorous technical and training standards and by second opinion reviews.


Subject(s)
Central Nervous System Vascular Malformations/diagnosis , Magnetic Resonance Angiography , Adult , Aged , Aged, 80 and over , False Negative Reactions , Female , Humans , Male , Middle Aged , Retrospective Studies , Spinal Cord/abnormalities
2.
Eur J Neurol ; 24(2): 391-396, 2017 02.
Article in English | MEDLINE | ID: mdl-28009079

ABSTRACT

BACKGROUND AND PURPOSE: Ethnicity-related differences in the incidence of acute disseminated encephalomyelitis (ADEM) and other demyelinating diseases including multiple sclerosis and neuromyelitis optica spectrum disorders have been reported. Little is reported on the influence of ethnicity and geographical location in ADEM. METHODS: Medical records of patients who presented with ADEM (ICD-9 323.61 and 323.81) at large referral hospitals in China, Singapore and Japan (years 1992-2015) were retrospectively reviewed and data were collected in a centralized database. Presenting features and outcomes of ADEM were compared between this multi-country Asian cohort and a uniformly collected US cohort using risk differences and risk ratios. Both cohorts were standardized to a 35% pediatric population to facilitate the comparison. RESULTS: There were 83 Asian patients (48 male, 16 pediatric) followed for a median of 2 (25th-75th percentile 1-10) months. Asian patients exhibited a 26% higher prevalence of spinal cord involvement on magnetic resonance imaging [95% confidence interval (CI) 0-52%; P = 0.05; 63% vs. 37%], a 39% lower prevalence of preceding events (95% CI 12-65%; P < 0.01; 33% vs. 72%) and a 23% lower prevalence of corpus callosum involvement (95% CI 7-39%; P < 0.01; 8% vs. 31%). No difference was observed between the two cohorts in the probability of relapse over the first year after disease onset. CONCLUSIONS: It is hypothesized that the high proportion of Asian patients with spinal cord lesions relates to genetic vulnerability or the higher incidence of neuromyelitis optica spectrum disorders in Asia or could be a spurious association. ADEM presentations most probably vary across geographical settings or ethnicities.


Subject(s)
Encephalomyelitis, Acute Disseminated/epidemiology , Adolescent , Adult , Age of Onset , Aged , Aged, 80 and over , Asian People , Child , Child, Preschool , China/epidemiology , Corpus Callosum/pathology , Databases, Factual , Encephalomyelitis, Acute Disseminated/pathology , Female , Humans , Incidence , Japan/epidemiology , Magnetic Resonance Imaging , Male , Middle Aged , Prevalence , Retrospective Studies , Risk Assessment , Singapore/epidemiology , Spinal Cord/pathology , Treatment Outcome , United States/epidemiology , Young Adult
3.
Rev Invest Clin ; 52(3): 229-33, 2000.
Article in Spanish | MEDLINE | ID: mdl-10953604

ABSTRACT

OBJECTIVES: To evaluate the hematological and clinical response to partial splenectomy in a group of children with hereditary spherocytosis. MATERIAL AND METHODS: We analyzed the main hematological and clinical features in 13 patients with hereditary spherocytosis submitted to partial splenectomy. The diagnosis of the disease and the hematological studies was made according to standard methods. To establish the inheritance pattern we also studied both parents. During the surgical procedure the upper two thirds of the spleen were removed and the lower pole was preserved. We use prophylactic penicillin (250 mg twice a day) during 3 years. RESULTS: The diagnosis of the disease was made during the first year of life in 11 patients, 76.9% had neonatal hyperbilirrubinemia, 53.8% showed hepatomegaly and in 69.2% we observed splenomegaly. 84.6% received blood transfusion. The hemoglobin level was significantly increased (p = 0.04) and the reticulocytes significantly diminished (p = 0.01) after splenectomy. No hemolytic crises, blood cell transfusion requirement neither infection was observed after surgery. CONCLUSIONS: Although the number of patients and the post-surgical follow-up is reduced, the hematological recovery observed in our cases suggest that partial splenectomy is a beneficial surgical procedure for the treatment of the typical and severe form of hereditary spherocytosis.


Subject(s)
Spherocytosis, Hereditary/surgery , Splenectomy/methods , Adolescent , Child , Child, Preschool , Female , Humans , Male
5.
An Esp Pediatr ; 45(3): 261-3, 1996 Sep.
Article in Spanish | MEDLINE | ID: mdl-9019966

ABSTRACT

OBJECTIVE: The aim of this study was to determine the usefulness of oxygen saturation (SaO2) in the assessment of a child with moderate laryngitis (croup). PATIENTS AND METHODS: A prospective study was carried out on 54 cases of moderate laryngitis (score of 2 to 6 of a possible 16) attended at our emergency department. Clinical score, heart rate, respiratory rate and SaO2 were recorded upon arrival. We analyzed the relationship between SaO2 and the requirement of nebulized epinephrine, parenteral dexamethasone and admission to the hospital. RESULTS: Patients who received epinephrine showed SaO2 values lower than those who did not (96.8 +/- 1.9 vs 97.9 +/- 1.7), although this was not a significant difference (p = 0.11). Similar findings were seen when the requirement of parenteral dexamethasone was analyzed (96.7 +/- 1.9 vs 97.3 +/- 1.8, p = 0.28). Children admitted to the hospital showed SaO2 values significantly lower than those discharged (96.5 +/- 1.9 vs 97.6 +/- 1.7, p = 0.03). No differences were seen when heart rate or respiratory rate were analyzed. CONCLUSIONS: We conclude that the measurement of is SaO2 useful in initial assessment of a child with acute laryngitis, essentially in order to better identify those patients who require admission to the hospital. It appears reasonable to include it in the initial assessment score.


Subject(s)
Laryngitis/metabolism , Oxygen/metabolism , Child, Preschool , Female , Humans , Infant , Male , Oximetry , Severity of Illness Index
SELECTION OF CITATIONS
SEARCH DETAIL
...