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2.
Leukemia ; 31(4): 903-912, 2017 04.
Article in English | MEDLINE | ID: mdl-27740636

ABSTRACT

Clinically useful pre-transplant predictive factors of acute graft-versus-host-disease (aGVHD) after allogeneic hematopoietic stem cell transplantation (allo-SCT) are lacking. We prospectively analyzed HSC graft content in CD34+, NK, conventional T, regulatory T and invariant natural killer T (iNKT) cells in 117 adult patients before allo-SCT. Results were correlated with occurrence of aGVHD and relapse. In univariate analysis, iNKT cells were the only graft cell populations associated with occurrence of aGVHD. In multivariate analysis, CD4- iNKT/T cell frequency could predict grade II-IV aGVHD in bone marrow and peripheral blood stem cell (PBSC) grafts, while CD4- iNKT expansion capacity was predictive in PBSC grafts. Receiver operating characteristic analyses determined the CD4- iNKT expansion factor as the best predictive factor of aGVHD. Incidence of grade II-IV aGVHD was reduced in patients receiving a graft with an expansion factor above versus below 6.83 (9.7 vs 80%, P<0.0001), while relapse incidence at two years was similar (P=0.5).The test reached 94% sensitivity and 100% specificity in the subgroup of patients transplanted with human leukocyte antigen 10/10 PBSCs without active disease. Analysis of this CD4- iNKT expansion capacity test may represent the first diagnostic tool allowing selection of the best donor to avoid severe aGVHD with preserved graft-versus-leukemia effect after peripheral blood allo-SCT.


Subject(s)
Graft vs Host Disease/immunology , Hematopoietic Stem Cell Transplantation/adverse effects , Natural Killer T-Cells/immunology , Tissue Donors , Acute Disease , Female , Graft vs Host Disease/diagnosis , Humans , Male , Natural Killer T-Cells/metabolism , Preoperative Period , Prognosis , Severity of Illness Index , Transplantation, Homologous
3.
J Med Life ; 8(3): 336-41, 2015.
Article in English | MEDLINE | ID: mdl-26351537

ABSTRACT

UNLABELLED: Intracranial aneurysm (IA) is a common vascular disorder, which frequently leads to fatal vascular rupture leading to subarachnoid hemorrhage (SAH). Although various acquired risk factors associated with IAs have been identified, heritable conditions are associated with IAs formation but these syndromes account for less than 1% of all IAs in the population. Cerebral aneurysm disease is related to hemodynamic and genetic factors, associated with structural weakness in the arterial wall, which was acquired by a specific, often unknown, event. Possibly, the trigger moment of aneurysm formation may depend on the dynamic arterial growth, which is closely related to aging/ atherosclerosis. Genetic factors are known to have an important role in IA pathogenesis. Literature data provide complementary evidence that the variants on chromosomes 8q and 9p are associated with IA and that the risk of IA in patients with these variants is greatly increased with cigarette smoking. Intracranial aneurysms are acquired lesions (5-10% of the population). In comparison with sporadic aneurysms, familial aneurysms tend to be larger, more often located in the middle cerebral artery, and more likely to be multiple. ABBREVIATIONS: DNA = deoxyribonucleic acid, FIA = familial Intracranial Aneurysm, GWAS = genome-wide association studies, IL-6 = interleukin-6, ISUIA = International Study of Unruptured Intracranial Aneurysms, IA = Intracranial aneurysm, mRNA = Messager ribonucleic acid, SNPs = single-nucleotide polymorphisms, SMCs = smooth muscle cells, sIAs = sporadic IAs, SAH = subarachnoid hemorrhage, TNF-α = tumor necrosis factor-alpha, COL4A1 = type IV collagen alpha-1.


Subject(s)
Genetic Predisposition to Disease , Intracranial Aneurysm/genetics , Animals , Humans , Inflammation/complications , Inflammation/pathology , Interleukins/metabolism , Intracranial Aneurysm/chemically induced , Intracranial Aneurysm/immunology , Myocytes, Smooth Muscle/pathology , Risk Factors
4.
Infection ; 42(4): 661-8, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24647770

ABSTRACT

OBJECTIVES: We wanted to assess the diagnostic accuracy of urinary dipstick testing in excluding catheter-associated urinary tract infection (CAUTI) in intensive care unit (ICU) patients with fever or hypothermia. METHODS: This was a prospective observational cohort study in a medical-surgical ICU. Patients with new-onset fever >38.3 °C or hypothermia <36 °C at least 48 h after urinary catheter insertion were included over a 2-year period. At each episode, a urinary dipstick test and a urine culture were performed as the criterion standard. Extensive microbiological investigations for extra-urinary infections were performed also. The performances of various urinary dipstick result combinations in ruling out CAUTI were compared based on the likelihood ratios (LR+ and LR-). RESULTS: Symptomatic CAUTI was diagnosed in 31 (24.4 %) of the 127 included patients (195 episodes of fever or hypothermia). LR+ was best for combined leukocyte esterase-positive and nitrite-positive dipstick results (overall population: 14.91; 95 % confidence interval [95 % CI], 5.53-40.19; patients without urinary symptoms: 15.63; 95 % CI, 5.76-42.39). LR- was best for either leukocyte esterase-positive or nitrite-positive dipstick results (overall population: 0.41; 95 % CI, 0.57-0.65; patients without urinary symptoms, 0.36; 95 % CI, 0.21-0.60). CONCLUSIONS: Urinary dipstick testing at the bedside does not help to rule out symptomatic CAUTI in medical or surgical ICU patients with fever or hypothermia.


Subject(s)
Catheter-Related Infections/diagnosis , Fever of Unknown Origin/etiology , Hypothermia/etiology , Point-of-Care Systems , Urinary Tract Infections/diagnosis , Urine/chemistry , Adult , Carboxylic Ester Hydrolases/analysis , Cohort Studies , Female , Humans , Intensive Care Units , Male , Microbiological Techniques , Middle Aged , Nitrites/analysis , Prospective Studies , Urine/microbiology
5.
Rev Mal Respir ; 26(1): 67-73, 2009 Jan.
Article in French | MEDLINE | ID: mdl-19212293

ABSTRACT

INTRODUCTION: Cystic fibrosis is usually diagnosed during the first years of life. Diagnosis may be achieved in adults with milder forms of the disease at any age. CASE REPORTS: We report the diagnosis of cystic fibrosis in three adults within the same family. A 39 yr old man, was diagnosed with congenital absence of the vas deferens; the diagnosis of cystic fibrosis was achieved based on a positive chloride sweat test and the identification of two mutations in the CFTR gene. His mother experienced repeated bronchial infections that began when she was 12 years old. The diagnosis of cystic fibrosis was considered at the age of 74 yr after her son was diagnosed with this disease. Sweat test showed normal chloride concentrations and cystic fibrosis was suspected based on elevated basal transepithelial nasal potential difference. Genetic testing for the 33 most frequent mutations in the CFTR gene showed only one mutation. A second rare mutation was identified by complete sequencing of the CFTR gene, confirming the diagnosis of cystic fibrosis. A third case of pauci-symptomatic cystic fibrosis was diagnosed in a brother of the index case. CONCLUSION: These observations illustrate the challenge of diagnosing milder forms of cystic fibrosis in adult subjects. The recognition of this diagnosis may lead to improvement in patient's care and to genetic counselling.


Subject(s)
Cystic Fibrosis/diagnosis , Cystic Fibrosis/genetics , Adult , Age Factors , Aged , Bronchiectasis/diagnostic imaging , Child , Chlorides/analysis , Cystic Fibrosis/diagnostic imaging , Cystic Fibrosis Transmembrane Conductance Regulator/genetics , Female , Genotype , Humans , Male , Middle Aged , Mutation , Pedigree , Radiography, Thoracic , Sweat/chemistry , Tomography, X-Ray Computed
6.
Childs Nerv Syst ; 23(3): 335-41, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17061134

ABSTRACT

INTRODUCTION AND BACKGROUND: Traumatic epidural hematoma (EDH) represents a rare head injury complication in infants. Its diagnosis can be quite challenging because its clinical presentation is usually subtle and nonspecific. In our current communication, we present our data regarding the presentation of infants with EDH, their management, and their long-term outcome. MATERIALS AND METHODS: In a retrospective study, the hospital and outpatient clinic charts and imaging studies (head CT and skull X-rays) of 31 infants with pure, supratentorial EDH of traumatic origin were meticulously reviewed. Children Coma Scale score and Trauma Infant Neurologic Score (TINS) were also reviewed. The most common presenting symptom was irritability, which occurred in 18/31 (58.1%) of our patients. Pallor (in 30/31 patients) and cephalhematoma (in 21/31 patients) were the most commonly occurring clinical signs upon admission; both signs represent signs of significant clinical importance. Surgical evacuation via a craniotomy was required in 24/31 of our patients, while 7/31 patients were managed conservatively. The mortality rate in our series was 6.5% (2/31 patients), and our long-term morbidity rate was 3.2% (1/31 patients). CONCLUSIONS: EDH in infants represents a life-threatening complication of head injury, which requires early identification and prompt surgical or conservative management depending on the patient's clinical condition, size of EDH, and presence of midline structure shift on head CT scan. Mortality and long-term morbidity are low with early diagnosis and prompt treatment.


Subject(s)
Decompression, Surgical/methods , Head Injuries, Closed/complications , Hematoma, Epidural, Cranial/diagnostic imaging , Skull Fractures/complications , Accidental Falls , Cerebellum/blood supply , Dura Mater/blood supply , Female , Follow-Up Studies , Head Injuries, Closed/diagnostic imaging , Head Injuries, Closed/therapy , Hematoma, Epidural, Cranial/etiology , Hematoma, Epidural, Cranial/therapy , Humans , Infant , Infant, Newborn , Male , Radiography , Retrospective Studies , Skull Fractures/diagnostic imaging , Trauma Severity Indices
7.
Acta Neurochir (Wien) ; 148(4): 421-6, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16374567

ABSTRACT

BACKGROUND: Cerebral hydatid cysts account for up to 3.6% of all intracranial space-occupying lesions, in endemic countries. The vast majority of patients affected are children. Computed tomography (CT) and magnetic resonance imaging (MRI) have greatly contributed to a more accurate diagnosis of hydatids. However, correct pre-operative diagnosis still remains quite puzzling. Extirpation of the intact cyst is the treatment of choice, resulting in most cases to a complete recovery. METHOD: In our retrospective study, we have reviewed 76 cases of intra-cranial hydatid disease operated on in our hospital over a 22 year period. Presenting clinical symptoms and signs and the radiological findings on CT and MRI were documented. Albendazole was given preoperatively to patients with giant (>5 cm) or multiple cysts and postoperatively to all patients. The follow-up period ranged from 12 months to 22 years and the outcome was assessed using the Glasgow Outcome Scale (GOS). FINDINGS: Sixty seven (95.7%) of our patients were children. Increased intracranial pressure and papilledema were the predominant findings in this group, whereas focal neurological deficits were most prevalent in adults. CT and MRI revealed round cystic lesions, isodense and iso-intense respectively to cerebrospinal fluid (CSF), with no rim enhancement or perifocal edema. Multiple cysts were identified in 3 cases. Extirpation of the cyst without rupture was accomplished in 56 patients (73.7%). Recurrences occurred in 19 patients (25%). 4 patients (5.3%) died within 6 months after surgery; 3 of these patients had multiple cysts and one died shortly after the operation due to anaphylactic shock following intra-operative rupture of the cyst. CONCLUSION: Long-term follow-up confirms that intracranial hydatid cysts should always be surgically removed without rupture; the outcome remains excellent in these cases. Correct preoperative diagnosis is vital for the successful outcome of surgery. A high index of suspicion is therefore required in endemic areas despite the availability of advanced neuro-imaging. Medical treatment with albendazole seems to be beneficial both pre- and post-operatively. Newer diagnostic methodologies, such as MR spectroscopy and MR diffusion weighted imaging, might lend themselves to the diagnosis of intracranial hydatid cysts.


Subject(s)
Brain/parasitology , Brain/surgery , Echinococcosis/surgery , Neurosurgical Procedures/adverse effects , Neurosurgical Procedures/statistics & numerical data , Adult , Albendazole/therapeutic use , Anticestodal Agents/therapeutic use , Brain/pathology , Child , Diagnosis, Differential , Echinococcosis/diagnosis , Echinococcosis/physiopathology , Female , Glasgow Outcome Scale , Humans , Magnetic Resonance Imaging , Male , Neurosurgical Procedures/mortality , Postoperative Complications/etiology , Postoperative Complications/mortality , Postoperative Complications/prevention & control , Preoperative Care/standards , Recurrence , Retrospective Studies , Therapeutic Irrigation/standards , Time , Tomography, X-Ray Computed , Treatment Outcome
8.
Acta Neurochir Suppl ; 93: 209-12, 2005.
Article in English | MEDLINE | ID: mdl-15986758

ABSTRACT

Authors present a seven years retrospective study on 85 cases of severe brain injuries (SBI) in children (GCS /= 20 mmHg, the Diffuse Axonal Injury (DAI) on MRI and the GCS on admission are factors of prognosis in SBI in children. The politrauma context is an aggravating factor for SBI in this age group. Other factors which influence GCS on admission may have prognostic importance i.e.: prehospital care, transport time and adequate transport conditions.


Subject(s)
Brain Injuries/diagnosis , Brain Injuries/mortality , Glasgow Coma Scale , Logistic Models , Outcome Assessment, Health Care/methods , Risk Assessment/methods , Adolescent , Brain Injuries/therapy , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Prognosis , Recovery of Function , Reproducibility of Results , Retrospective Studies , Risk Factors , Romania/epidemiology , Sensitivity and Specificity , Severity of Illness Index , Treatment Outcome
9.
Virologie ; 31(2): 95-102, 1980.
Article in English | MEDLINE | ID: mdl-6250281

ABSTRACT

The Romanian BL-VACC-RO vaccine against bovine leukemia virus (BLV) infection was prepared with ethylenimine-inactivated BLV obtained from persistently infected cell lines. Intramuscular administration of two vaccine doses (each containing 0.40 mg virus glycoprotein with adjuvant), 2 weeks apart, conferred protection against challenge infection with BLV on 18 of the 20 vaccinated calves. Two calves were not protected, in spite of their positive serologic response to vaccination. The results demonstrate the efficiency of the BL-VACC-RO vaccine in preventing BLV infection.


Subject(s)
Cattle Diseases/prevention & control , Leukemia Virus, Bovine/immunology , Leukemia/veterinary , Retroviridae/immunology , Viral Vaccines , Animals , Cattle , Leukemia/prevention & control , Vaccination
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