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1.
Malays J Pathol ; 45(1): 31-41, 2023 Apr.
Article En | MEDLINE | ID: mdl-37119244

INTRODUCTION: The treatment of Plasmodium vivax malaria with 8-aminoquinolines is contraindicated in glucose-6-phosphate dehydrogenase (G6PD) deficient individuals due to the risk of acute haemolytic anaemia. Effective G6PD screening is paramount to avoid adverse drug reactions. This study aimed to evaluate the performance of novel quantitative point-of-care (POC) tests as a new screening method for G6PD deficiency in Malaysia. MATERIALS AND METHODS: A total of 153 neonatal cord blood, 99 peripheral blood of older children aged between 1 month to 12-years old, and 62 peripheral adult blood were screened for G6PD deficiency using two quantitative POC tests, CareStartTM biosensor (Carestart) and CareStartTM Biosensor 1 (S1). The results were compared with OSMMR2000D kit as a reference assay. Two statistical analyses were performed in this study to evaluate the POC test performances, the Spearman's correlation test and the Cohen's kappa method. RESULTS: Both Carestart and S1 tests showed significant positive correlations to OSMMRS000D with r2 = 0.7916 and r2 = 0.7467. Their measurement of agreement showed a kappa (κ) value of 0.805 (p<0.001, 95% CI), and 0.795 (p<0.001, 95% CI), respectively. Analysis of the area under the Receiver Operating Curve (ROC) at 60% cut-off illustrated that the Carestart had 90.2% sensitivity, 98.9% specificity, 98.3% positive predictive value (PPV), and 93.8% negative predictive value (NPV). The corresponding values for the S1 were 95.2%, 100%, 100%, and 96.8%, respectively. CONCLUSION: This study showed that the Carestart and S1 biosensors have high-performance reliability for screening of G6PD deficiency, which can guide safe prescriptions of anti-malaria medications and hence, eradication of Plasmodium vivax malaria.


Glucosephosphate Dehydrogenase Deficiency , Malaria, Vivax , Adult , Child , Infant, Newborn , Humans , Adolescent , Infant , Glucosephosphate Dehydrogenase Deficiency/diagnosis , Glucosephosphate Dehydrogenase/therapeutic use , Malaria, Vivax/diagnosis , Malaria, Vivax/drug therapy , Reproducibility of Results , Malaysia , Point-of-Care Testing
2.
ACS Omega ; 7(35): 31327-31337, 2022 Sep 06.
Article En | MEDLINE | ID: mdl-36092592

One of the inevitable problems encountered during the petroleum well drilling process is "lost circulation" in which part of the drilling fluid is lost into the formation. A combination of nanoparticles with their unique properties and cost-effective biodegradable materials can play an effective role in treating fluid loss. In this study, our aim was to formulate drilling fluids modified with nanoparticles, pomegranate peel powder, and Prosopis farcta plant powder. The drilling fluids were identified and recognized using scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy techniques. Furthermore, experimental tests were conducted in order to investigate the performance of the newly formulated drilling fluid in improving fluid loss characteristics. The obtaining results have shown that adding 0.3 wt % of pomegranate peel powder to the reference (base) drilling fluid reduces the filter loss volume to 7.9 mL compared to the reference fluid (11.6 mL). As the optimal concentration of TiO2 was mixed with 0.3 wt % of pomegranate peel powder then added to the reference fluid, the filter loss volume was reduced to 8.6 mL.

3.
J Food Sci Technol ; 59(7): 2724-2730, 2022 Jul.
Article En | MEDLINE | ID: mdl-35734105

In this study, the aflatoxin contamination level of selected freshly harvested and dried African leafy vegetables was investigated after inoculation with Aspergillus flavus spores and incubation at 32%, 74%, 84%, and 96% static relative humidity. The study question was whether Aspergillus sp. growth on selected vegetables: Corchorus olitorius, Crotalaria ochroleuca, Vigna unguiculata, Solanum villosum, and Amaranthus blitum can produce aflatoxins. The experiment was replicated thrice and a control sample was included for each replicate. An Agilent 1260 Infinity HPLC system was used for analysis and we quantified the following aflatoxins; B1, B2, G1, and G2 in the selected vegetables. Our results show that aflatoxin B1, G1, and G2 were all present, with the B1 being prevalent. The contamination level increased with relative humidity increase for both freshly harvested and dried vegetables. However, the dried vegetables had a lower contamination level in comparison with freshly harvested. The findings affirm the importance of post-harvest crop preservation to avoid mycotoxin contamination. The vegetables can suffer aflatoxin contamination when exposed to high moisture and ambient temperature and drying is a suitable method of vegetable preservation.

4.
Article En | MEDLINE | ID: mdl-35319492

Summary: Von Hippel-Lindau's disease (VHL) is a hereditary tumor syndrome characterized by its prototype lesions, hemangioblastomas, and renal cell carcinomas. Treatment for renal cell carcinomas can ultimately result in long-term dialysis. Pancreatic neuroendocrine tumors (pNET) can also occur in the course of the disease. Currently, peptide receptor radionuclide therapy (PRRT) is the standard treatment for progressive neuroendocrine tumors. However, little is known about treatment with PRRT in patients on dialysis, an infrequent presentation in patients with VHL. We present a 72-year-old man with VHL on hemodialysis and a progressive pNET. He received four cycles of PRRT with a reduced dose. Only mild thrombopenia was seen during treatments. The patient died 9 months after the last PRRT because of acute bleeding in a hemangioblastoma. Hemodialysis is not a limiting factor for PRRT treatment and it should be considered as it seems a safe short-term treatment option for this specific group. Learning points: Von Hippel-Lindau disease (VHL) is a complex disease in which former interventions can limit optimal treatment for following VHL-related tumors later in life. Metastasized pancreatic neuroendocrine tumors occur as part of VHL disease. Peptide receptor radionuclide therapy seems a safe short-term treatment option in patients on hemodialysis.

5.
Eur J Neurol ; 27(8): 1570-1577, 2020 08.
Article En | MEDLINE | ID: mdl-32359218

BACKGROUND AND PURPOSE: Epilepsy is most common in lower-income settings where access to electroencephalography (EEG) is generally poor. A low-cost tablet-based EEG device may be valuable, but the quality and reproducibility of the EEG output are not established. METHODS: Tablet-based EEG was deployed in a heterogeneous epilepsy cohort in the Republic of Guinea (2018-2019), consisting of a tablet wirelessly connected to a 14-electrode cap. Participants underwent EEG twice (EEG1 and EEG2), separated by a variable time interval. Recordings were scored remotely by experts in clinical neurophysiology as to data quality and clinical utility. RESULTS: There were 149 participants (41% female; median age 17.9 years; 66.6% ≤21 years of age; mean seizures per month 5.7 ± SD 15.5). The mean duration of EEG1 was 53 ± 12.3 min and that of EEG2 was 29.6 ± 12.8 min. The mean quality scores of EEG1 and EEG2 were 6.4 [range, 1 (low) to 10 (high); both medians 7.0]. A total of 44 (29.5%) participants had epileptiform discharges (EDs) at EEG1 and 25 (16.8%) had EDs at EEG2. EDs were focal/multifocal (rather than generalized) in 70.1% of EEG1 and 72.5% of EEG2 interpretations. A total of 39 (26.2%) were recommended for neuroimaging after EEG1 and 22 (14.8%) after EEG2. Of participants without EDs at EEG1 (n = 53, 55.8%), seven (13.2%) had EDs at EEG2. Of participants with detectable EDs on EEG1 (n = 23, 24.2%), 12 (52.1%) did not have EDs at EEG2. CONCLUSIONS: Tablet-based EEG had a reproducible quality level on repeat testing and was useful for the detection of EDs. The incremental yield of a second EEG in this setting was ~13%. The need for neuroimaging access was evident.


Epilepsy , Adolescent , Electroencephalography , Epilepsy/diagnosis , Female , Guinea , Humans , Male , Reproducibility of Results , Seizures/diagnosis
6.
Aliment Pharmacol Ther ; 33(8): 946-53, 2011 Apr.
Article En | MEDLINE | ID: mdl-21342211

BACKGROUND: Adalimumab is efficacious therapy for adults with Crohn's disease (CD). AIM: To summarise the United Kingdom and Republic of Ireland paediatric adalimumab experience. METHODS: British Society of Paediatric Gastroenterology, Hepatology and Nutrition (BSPGHAN) members with Inflammatory Bowel Disease (IBD) patients <18 years old commencing adalimumab with at least 4 weeks follow-up. Patient demographics and details of treatment were then collected. Response and remission was assessed using the Paediatric Crohn's Disease Activity Index (PCDAI)/Physicians Global Assessment (PGA). RESULTS: Seventy-two patients [70 CD, 1 ulcerative colitis (UC), 1 IBD unclassified (IBDU)] from 19 paediatric-centres received adalimumab at a median age of 14.8 (IQR 3.1, range 6.1-17.8) years; 66/70 CD (94%) had previously received infliximab. A dose of 80 mg then 40 mg was used for induction in 41(59%) and 40 mg fortnightly for maintenance in 61 (90%). Remission rates were 24%, 58% and 41% at 1, 6 and 12 months, respectively. Overall 43 (61%) went into remission at some point, with 24 (35%) requiring escalation of therapy. Remission rates were higher in those on concomitant immunosuppression cf. those not on immunosuppression [34/46 (74%) vs. 9/24 (37%), respectively, (χ(2) 8.8, P=0.003)]. There were 15 adverse events (21%) including four (6%) serious adverse events with two sepsis related deaths in patients who were also on immunosuppression and home parenteral nutrition (3% mortality rate). CONCLUSIONS: Adalimumab is useful in treatment of refractory paediatric patients with a remission rate of 61%. This treatment benefit should be balanced against side effects, including in this study a 3% mortality rate.


Anti-Inflammatory Agents/administration & dosage , Antibodies, Monoclonal/administration & dosage , Inflammatory Bowel Diseases/drug therapy , Adalimumab , Adolescent , Antibodies, Monoclonal, Humanized , Child , Child, Preschool , Female , Health Surveys , Humans , Ireland , Male , Remission Induction , Severity of Illness Index , Treatment Outcome , United Kingdom
7.
Mol Biol Rep ; 38(2): 1367-74, 2011 Feb.
Article En | MEDLINE | ID: mdl-20632114

α- and ß-Galactosidases find application in food processing, health and nutrition. Aspergillus niger is one of the potent producer of these enzymes and was genotypically improved using gamma-ray induced mutagenesis. The mutant-derivative produced two-fold higher α- and ß-galactosidases. For testing genetic variability and its relationship with phenotypic properties of the two organisms, DNA samples of the mutant and parental strains of A. niger were amplified with 28 deca-nucleotide synthetic primers. RAPD analysis showed significantly different pattern between parental and mutant cultures. The mutant derivative yielded homogeneous while parental strain formed heterogeneous amplification patterns. Seven primers identified 42.9% polymorphism in the amplification products, indicating that these primers determined some genetic variability between the two strains. Thus RAPD was found to be an efficient technique to determine genetic variability in the mutant and wild organisms. Both wild and mutant strains were analyzed for their potential to produce galactosidases. Comparison of different carbon sources on enzyme yield revealed that wheat bran is significant (P < 0.01) effective producer and economical source followed by rice bran, rice polishing and lactose. The mutant was significantly better enzyme producer and could be considered for its prospective application in food, nutrition and health and that RAPD can be effectively used to differentiate mutant strain from the parental strain based on the RAPD patterns.


Aspergillus niger/genetics , Industrial Microbiology/methods , Mutagenesis , Culture Media , DNA/genetics , DNA/metabolism , Fermentation , Galactosidases/metabolism , Gamma Rays , Genetic Variation , Kinetics , Mutagenesis, Site-Directed , Mutation , Polymorphism, Genetic , Random Amplified Polymorphic DNA Technique/methods , Thermodynamics
8.
J R Soc Health ; 117(4): 242-4, 1997 Aug.
Article En | MEDLINE | ID: mdl-9375488

The case report is presented of a ten-and-a-half year old boy with acute onset of confusion and visual hallucinations, subsequently confirmed to be due to hyoscine toxicity following ingestion of over-the-counter (OTC) travel sickness tablets. It is suggested that packs of such pills should carry a prominent cautionary label. A clear clinical history is very important--not only in aiding the differentiation of acute viral infections involving the central nervous system (such as acute encephalitis) from drug toxicity, but also in rationalizing any further diagnostic investigations. The possible underlying reasons for drug ingestion in this case are discussed.


Antiemetics/poisoning , Nonprescription Drugs/poisoning , Scopolamine/poisoning , Child , Confusion/etiology , Hallucinations/etiology , Humans , Male , Poisoning/diagnosis
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