scholarly journals Sensitivity of life-long diagnostic methods for geese nematodes

2019 ◽  
Vol 2 (3) ◽  
pp. 39-42
Author(s):  
O. B. Prijma
Keyword(s):  
Final Stage ◽  
Comparative Evaluation ◽  
Animal Species ◽  
Prolonged Exposure ◽  
Laboratory Diagnosis ◽  
Diagnostic Methods ◽  
Sugar Solution ◽  
Main Indicator ◽  
Nematode Eggs

The basis of successful struggle and specific prevention of poultry worms is timely diagnosis, the final stage of which is the detection of the worms themselves, their eggs or larvae at various stages of development. Priority is given to the methods of lifelong laboratory diagnosis of helminthiasis, which are preferably recommended for use in all animal species, including poultry. The aim of this work was to determine the sensitivity of flotation methods of coprovoscopy for geese nematodes. Experimental determination of the efficiency of the well-known methods of flotation and their comparative evaluation of coproovoscopic diagnosis of heterocosis, capillary disease and trichostrongilosis of geese. The main indicator of the diagnostic effectiveness of the methods was the intensity of the invasion and the time spent on the flotation of the samples. The most effective methods for diagnosing geese geoccosis are Kotelnikov-Hrenov (with ammonium nitrate) – at exposures of 20 min and Mallory (with saturated sugar solution) – at exposures of 10–15 min. The rates of invasion intensity were respectively 62.0 ± 4.39 and 59.0 ± 3.47 eggs/g. In the laboratory diagnosis of goose capillary disease, the most sensitive methods were Kotelnikov-Hrenov and Mallory at exposures of 15–20 min, where infestation rates reached 34.0 ± 2.22 and 33.5 ± 2.64 eggs/g, respectively. For trichostrongilosis, the Kotelnikov-Hrenov method showed the highest sensitivity at the exposure of 20 min, the intensity of the invasion was 32.5 ± 3.23 eggs/g. The Mallory method proved to be less effective – at an exposure of 15 min poultry invasiveness was 23.5 ± 1.81 eggs/g. The least sensitive of this invasion was the Fulleborn method (with NaCl), where the intensity of the invasion gradually increased with prolonged exposure and ranged from 10.5 ± 0.5 to 19.5 ± 2.45 eggs/g. Based on the data obtained, it is recommended to use the most sensitive methods and to take into account the exposure, which ensures the concentration of the largest number of nematode eggs on the surface of the flotant when conducting life-long coproovoscopic diagnostics of heterosis, capillary disease and trichostrongilosis of geese.

EVALUATION OF HYSTEROSALPINGOGRAPHY VERSUS LAPAROSCOPY IN THE DETERMINATION OF TUBAL FACTORS IN FEMALE INFERTILITY: A HOSPITAL BASED COMPARATIVE STUDY.

2020 ◽  
Vol 4 (9) ◽  
Author(s):  
Richa Choudhary ◽  
Rishikant Sinha
Keyword(s):  
Female Infertility ◽  
Diagnostic Methods ◽  
Panoramic View ◽  
Tubal Patency ◽  
Pelvic Organs ◽  
Clinical Investigations ◽  
Detailed Assessment ◽  
Reproductive Anatomy ◽  
Tubal Pathology

Objectives: Hysterosalpingography and laparoscopy both are the diagnostic methods for assessment of female infertility.  The present study was to compare the evaluation of hysterosalpingography (HSG) versus laparoscopy in determination of tubal factors in female infertility. Methods: Detailed assessment, physical examination and clinical investigations were performed in all 100 infertile female with age 20 years to 40 years. All patients were advised to perform digital HSG. Patients with an abnormal HSG underwent laparoscopy without delay, whereas in patients with a normal HSG, laparoscopy was performed three months after HSG. HSG is best scheduled during the 2nd -5th day interval immediately following the end of menstruation, to minimize risk for infection, avoid interference from intrauterine blood and clot, and to prevent any possibility that the procedure might be performed after conception. Results: Data was analysed by using IBM SPSS version 23 software.  All data was tabulated and percentages were calculated. Mean ± standard deviation was observed. Conclusions: Diagnostic laparoscopy is the gold standard in diagnosing tubal pathology and other intra-abdominal causes of infertility. Other hand, Hysterosalpingography is a frequently utilized diagnostic tool in the assessment of tubal status and detection of uterine anatomical defects in infertility. Hysterosalpingography and laparoscopy are not alternatives but complimentary investigations. But, inadequacy of hysterosalpingography (HSG) in determining the state of tubal patency, emphasizes the need for laparoscopy. Laparoscopy provides both a panoramic view of the pelvic reproductive anatomy and a magnified view of pelvic organs and peritoneal surfaces. Keywords: Female infertility, Tubal patency, HSG, Laparoscopy

Determination of the profile of the temperature field of material heated by continuous laser radiation

2020 ◽  
pp. 51-10
Author(s):  
B.A. Lapshinov ◽  
◽  
N.I. Timchenko ◽  
Keyword(s):  
Temperature Field ◽  
Optical Fiber ◽  
Prolonged Exposure ◽  
Radiation Spectrum ◽  
Visible Range ◽  
Continuous Laser ◽  
Surface Temperature Distribution ◽  
Continuous Radiation ◽  
Spectral Pyrometry

Spectral pyrometry was used to determine the surface temperature distribution of Si, Nb, Cu, and graphite samples when they were locally heated by continuous radiation of an Nd:YAG laser (λ = 1.064 μm). With prolonged exposure to radiation, a stationary temperature field was established in the samples. The thermal spectra were recorded with a small spectrometer in the visible range in the temperature range above 850 K. The optical fiber used to transmit the radiation spectrum to the spectrometer had an additional diaphragm with a diameter of 1 mm located at a certain distance from the fiber end, which ensured the locality of the recorded spectra. The optical fiber moved continuously along the sample, and the spectrometer recorded up to 100 spectra with a frequency of 5-10 Hz. The temperature profile of the samples was calculated based on the results of processing the spectra using the Spectral Pyrometry program.

scholarly journals Differential Laboratory Diagnosis of Acute Fever in Guinea: Preparedness for the Threat of Hemorrhagic Fevers

2021 ◽  
Vol 18 (11) ◽  
pp. 6022
Author(s):  
Vladimir G. Dedkov ◽  
N’Faly Magassouba ◽  
Olga A. Stukolova ◽  
Victoria A. Savina ◽  
Jakob Camara ◽  
...  
Keyword(s):  
Ebola Virus ◽  
Febrile Illness ◽  
Laboratory Diagnosis ◽  
Acute Febrile Illness ◽  
Causative Pathogen ◽  
Hemorrhagic Fevers ◽  
Wide Range ◽  
Causative Agents ◽  
Pathognomonic Sign

Acute febrile illnesses occur frequently in Guinea. Acute fever itself is not a unique, hallmark indication (pathognomonic sign) of any one illness or disease. In the infectious disease context, fever’s underlying cause can be a wide range of viral or bacterial pathogens, including the Ebola virus. In this study, molecular and serological methods were used to analyze samples from patients hospitalized with acute febrile illness in various regions of Guinea. This analysis was undertaken with the goal of accomplishing differential diagnosis (determination of causative pathogen) in such cases. As a result, a number of pathogens, both viral and bacterial, were identified in Guinea as causative agents behind acute febrile illness. In approximately 60% of the studied samples, however, a definitive determination could not be made.

Possibilities of cytological diagnostics in gynecology. Human papillomavirus as an interdisciplinary problem

2022 ◽  
pp. 15-21
Author(s):  
Oksana Anatolievna Gizinger ◽  
◽  
Irina Yurievna Lepina ◽  
Marina Nikolaevna Bagdasaryan ◽  
◽  
...  
Keyword(s):  
Human Papillomavirus ◽  
Screening Test ◽  
Molecular Genetic ◽  
Laboratory Diagnosis ◽  
Diagnostic Methods ◽  
Laboratory Diagnostics ◽  
Cytological Examination ◽  
Stage Of Development ◽  
Current Stage ◽  
Cytological Diagnostics

The article presents an analysis of current information on the etiology, pathogenesis, laboratory diagnosis of human papillomavirus. It is shown that at the current stage of development of laboratory diagnostics there is a reliable screening test — cytological examination of smears taken from the ecto- and endocervix. To diagnose HPV, a combination of microscopic (cytological studies) and molecular genetic (PCR) diagnostic methods is used.

MO432COMPARATIVE ANALYSIS OF INDIRECT IMMUNOFLUORESCENCE AND ENZYME-LINKED IMMUNOSORBENT ASSAYS FOR ANTI-PLA2R ASSESMENT IN PATIENTS WITH PRIMARY MEMBRANOUS NEPHROPATHY

2021 ◽  
Vol 36 (Supplement_1) ◽  
Author(s):  
Olga Galkina ◽  
Evdokia Bogdanova ◽  
Irina Zubina ◽  
Elena Levykina ◽  
Alexei Smirnov
Keyword(s):  
Indirect Immunofluorescence ◽  
Membranous Nephropathy ◽  
Laboratory Diagnosis ◽  
Response To Therapy ◽  
Control Group ◽  
Course Of Disease ◽  
Phospholipase A2 Receptor ◽  
Gender And Age ◽  
Positive Results

Abstract Background and Aims Antibodies to M-type phospholipase A2 receptor (PLA2R-Ab) are considered to be a promising biomarker for laboratory diagnosis of primary membranous nephropathy (PMN) and may be useful in the evaluation of the response to therapy and CKD prognosis. The aim of the study was to compare two immunoassay methods – indirect immunofluorescence (IIF) and enzyme immunoassay (ELISA) for the determination of circulating PLA2R-Ab in patients with PMN. Method The study included 54 patients aged 55 (40-63) yrs. (M: F [33:21]) with PMN before treatment (n=16) and treated with immunosuppressive therapy (IST) (n=38), and apparently healthy individuals of the corresponding gender and age (n=10). Proteinuria and estimated glomerular filtration rate (eGFR) were determined in all participants. The levels of PLA2R-Ab were determined by IIF and quantitative/ semi-quantitative ELISA (EURUIMMUN AG test, Germany). In 16 PMN patients without treatment and 28 PMN patients treated with IST the level of PLA2R-Ab was measured one time and in 10 PMN patients treated IST – in dynamic, from 2 to 5 times. Statistical comparisons among groups were performed using Mann–Whitney U-test and Kruskal-Wallis H tests. The association between variables was estimated using Spearman’s coefficient. Sensitivity and specificity of the methods were calculated. Results The correlation coefficient between IIF and ELISA was 0.82 (p <0.005). There were more PLA2R-Ab-positive cases detected by ELISA, both before treatment (ELISA - 80%, IIF - 67%) and among patients treated with IST (ELISA - 63%, IIF - 50%). In control group, ELISA showed no positive results for PLA2R-Ab (specificity was 100%). The levels of proteinuria and eGFR were associated with autoantibodies determined by ELISA, both quantitative and semi-quantitative (proteinuria: r = 0.69, p = 0.001; eGFR: r = -0.38, p = 0.035) but not by IIF (proteinuria: r=0.33, p=0.061; eGFR: r=-0.26, p=0.082). The levels of PLA2R-Ab measured by ELISA correlated with the course of disease in patients treated with IST, while IIF did not show any dynamics is some cases. Conclusion Both quantitative and semi-quantitative ELISA were considered to be more preferable methods since the obtained results correlate with renal dysfunction and allow to assess the concentration of PLA2R-Ab in the course of disease more accurately, that may contribute to timely correction of treatment and improvement of outcome.

scholarly journals Comparative evaluation of conventional RT-PCR and real-time RT-PCR (RRT-PCR) for detection of avian metapneumovirus subtype A

2009 ◽  
Vol 39 (5) ◽  
pp. 1445-1451 ◽  
Author(s):  
Helena Lage Ferreira ◽  
Fernando Rosado Spilki ◽  
Márcia Mercês Aparecida Bianchi dos Santos ◽  
Renata Servan de Almeida ◽  
Clarice Weis Arns
Keyword(s):  
Real Time ◽  
Comparative Evaluation ◽  
Virus Isolation ◽  
Diagnostic Methods ◽  
N Gene ◽  
Genomic Rna ◽  
Rt Pcr ◽  
Avian Metapneumovirus ◽  
Lower Detection ◽  
Subtype A

Avian metapneumovirus (AMPV) belongs to Metapneumovirus genus of Paramyxoviridae family. Virus isolation, serology, and detection of genomic RNA are used as diagnostic methods for AMPV. The aim of the present study was to compare the detection of six subgroup A AMPV isolates (AMPV/A) viral RNA by using different conventional and real time RT-PCR methods. Two new RT-PCR tests and two real time RT-PCR tests, both detecting fusion (F) gene and nucleocapsid (N) gene were compared with an established test for the attachment (G) gene. All the RT-PCR tested assays were able to detect the AMPV/A. The lower detection limits were observed using the N-, F- based RRT-PCR and F-based conventional RT-PCR (10(0.3) to 10¹ TCID50 mL-1). The present study suggests that the conventional F-based RT-PCR presented similar detection limit when compared to N- and F-based RRT-PCR and they can be successfully used for AMPV/A detection.

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