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Institution

Bethesda Hospital

HealthcareAmbur, Tamil Nadu, India
About: Bethesda Hospital is a healthcare organization based out in Ambur, Tamil Nadu, India. It is known for research contribution in the topics: Population & Helicobacter pylori. The organization has 386 authors who have published 472 publications receiving 15193 citations.


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Journal ArticleDOI
TL;DR: Anal chromoendoscopy is safe and effective in diagnosing AIN in a population of HIV-infected patients and may become a valuable new tool to manage AIN and to prevent anal malignancy in HIV-positive patients.
Abstract: Introduction Anal carcinoma represents an increasing problem in HIV-infected patients. Anal intraepithelial neoplasia (AIN), the precursor lesion, is currently diagnosed by high-resolution anoscopy (HRA) using optical magnification derived from gynecological colposcopy. This prospective study evaluates anal chromoendoscopy (ACE) using standard gastroenterological video-endoscopes in diagnosing AIN. Methods After clinical examination, proctoscopy and surface staining with acetic acid followed by Lugol’s solution, ACE was performed with a mucosectomy cap on the tip of the endoscope. Biopsy specimens were collected from areas with a pathological staining pattern and from areas with normal appearance; combined results were considered as reference. Results Two hundred eleven HIV-positive patients seen between 2007 and 2013 were evaluated. Of these, 95.7 % were males, and the median age was 45 years. In 86.7 %, the mode of HIV transmission was sex among males. Combination antiretroviral treatment was applied in 75.8 %. The sensitivity of ACE in diagnosing AIN was 0.85, the specificity was 0.55, the positive predictive value was 0.50, and the negative predictive value (NPV) was 0.87. Diagnostic performance increased in individuals with high-grade lesions (NPV: 0.99) and in the second study period from 2011 to 2013. Side effects were rare and of minor clinical relevance. Conclusions Anal chromoendoscopy is safe and effective in diagnosing AIN in a population of HIV-infected patients. It is particularly useful for the exclusion of high-grade lesions that have the strongest risk of progression to anal carcinoma. Therefore, ACE may become a valuable new tool to manage AIN and to prevent anal malignancy in HIV-positive patients.

8 citations

Journal ArticleDOI
TL;DR: It is hypothesized that altered splice products may not be expressed as functional receptors at the cell surface because of the high degree of similarity for the epsilon(IVS7-2A/G) carrying allele in all families and may therefore indicate a common origin of the mutation.
Abstract: Mutations in the epsilon-acetylcholine receptor (AChR epsilon) subunit gene cause congenital myasthenic syndromes (CMS) with postsynaptic neural transmission defects. We present 3 male and 2 female patients from three unrelated Croatian, Hungarian, and Russian families with autosomal recessive CMS. All patients manifested with variable degrees of ophthalmoparesis and generalized, fatiguable muscle weakness since birth or early infancy. Electrophysiological studies showed a decremental response in all patients indicating a neuromuscular transmission defect. Pyridostigmine treatment improved the proximal muscle weakness whereas the ophthalmoparesis remained unchanged in all patients. Analysis of the AChR epsilon subunit gene showed homozygosity for a novel splice site mutation of intron 7 epsilon(IVS7-2A/G) in the two Croatian siblings. epsilon-mRNA analysis by RT-PCR and direct sequencing revealed that exon 7 was spliced directly to exon 9 with skipping of exon 8. The Hungarian and Russian patients were heteroallelic carriers of the same mutation epsilon(IVS7-2A/G) and of a frameshifting mutation epsilon 70insG and epsilon 1293insG, respectively. We hypothesize that altered splice products may not be expressed as functional receptors at the cell surface. A haplotype analysis with polymorphic markers revealed a high degree of similarity for the epsilon(IVS7-2A/G) carrying allele in all families and may therefore indicate a common origin of the mutation.

8 citations

Journal ArticleDOI
TL;DR: The limitations of conventional neuropsychological assessment in predicting disabilities have been demonstrated in a number of studies and possible solutions to this problem are discussed critically.
Abstract: The development of clinical neuropsychology has shown a gradually changing emphasis, from tests of organicity, through actuarial approaches, towards a more flexible approach, which utilises qualitative observations of patient behaviour. In recent years clinical neuropsychologists have played a greater role in patient management, in addition to diagnosis, particularly in the rehabilitation setting. The emphasis has thus changed gradually from measurement to application. Relationships between test performance and functional efficiency in daily life have not always been addressed, however. The focus tends to be on “impairment” as opposed to “disability”. The limitations of conventional neuropsychological assessment in predicting disabilities have been demonstrated in a number of studies. Possible solutions to this problem are discussed critically. These include the use of behavioural observation, rating scales or checklists. and standardised assessment procedures that simulate everyday activities. I...

8 citations

Journal ArticleDOI
TL;DR: This study aimed to assess whether people initiated with CD4 counts >500 cells/µL had worse treatment outcomes compared to those initiated at lower CD4 count.
Abstract: Introduction The World Health Organisation recommends to Treat All people with HIV, irrespective of CD4 count. However, people with CD4 counts >500 cells/µL may be asymptomatic and therefore less motivated to adhere to antiretroviral therapy (ART). We aimed to assess whether people initiated with CD4 counts >500 cells/µL had worse treatment outcomes compared to those initiated at lower CD4 counts. Methods We performed a retrospective cohort study among non-pregnant adults initiating ART at eight public clinics in South Africa between September 2016, when Treat All was implemented, and August 2017. We assessed whether initiation CD4 count >500 cells/µL was associated with the outcomes of attrition (death, lost to follow-up or treatment interruption >180 days), and viraemia >1000 copies/mL, by twelve months using Cox proportional hazards and Poisson regression models. Results and discussion Among 4952 patients initiating ART, the median age was 32.4 years (interquartile range (IQR) 27.2 to 39.7), 58.9% were women and 30.3% had an initiation CD4 count >500 cells/µL. After twelve months, 3382 (68.3%) were retained in care, 303 (6.1%) had transferred to another clinic, 1010 (20.4%) were lost to follow-up, 232 (4.7%) had a treatment interruption >180 days and 25 (0.5%) were known to have died. Overall, 1267 experienced attrition at a median time of 91 days (IQR 23 to 213), with 302 of these (23.8%) experiencing attrition immediately after their ART initiation visit. Among those in care at twelve months with viral load results, 4.6% had viraemia. In multivariable analysis, the hazard of attrition was similar between patients newly eligible for ART with CD4 counts >500 cells/µL compared to those with CD4 ≤500 cells/µL (adjusted hazard ratio 1.03, 95% confidence interval (CI) 0.90 to 1.17). The risk of viraemia was lower among patients with CD4 counts >500 cells/µL compared to those with CD4 ≤500 cells/µL (adjusted risk ratio 0.58, 95% CI 0.37 to 0.92). Conclusions After implementation of Treat All in South African public clinics, we found that patients newly eligible for ART with initiation CD4 counts >500 cells/µL had comparable or better outcomes compared to those with lower CD4 counts. These finding support ongoing implementation of Treat All in our setting.

8 citations

Journal ArticleDOI
TL;DR: International estimates of the laparoscopic radical prostatectomy learning curve extend to as many as 1000 cases, but is unknown for Fellowship‐trained Australian surgeons.
Abstract: International estimates of the laparoscopic radical prostatectomy (LRP) learning curve extend to as many as 1000 cases, but is unknown for Fellowship-trained Australian surgeons Prospectively collected data from nine Australian surgeons who performed 2943 consecutive LRP cases was retrospectively reviewed Their combined initial 100 cases (F100, n = 900) were compared to their second 100 cases (S100, n = 782) with two of nine surgeons completing fewer than 200 cases The mean age (611 versus 611 years) and prostate specific antigen (74 versus 78 ng/mL) were similar between F100 and S100 D'Amico's high-, intermediate- and low-risk cases were 15, 59 and 26% for the F100 versus 20, 59 and 21% for the S100, respectively Blood transfusions (24 versus 08%), mean blood loss (413 versus 378 mL), mean operating time (193 versus 163 min) and length of stay (27 versus 24 days) were all lower in the S100 Histopathology was organ confined (pT2) in 76% of F100 and 71% of S100 Positive surgical margin (PSM) rate was 184% in F100 versus 175% in the S100 (P = 062) F100 and S100 PSM rates by pathological stage were similar with pT2 PSM 122 versus 95% (P = 013), pT3a PSM 348 versus 405% (P = 029) and pT3b PSM 529 versus 364% (P = 014) There was no significant improvement in PSM rate between F100 and S100 cases Perioperative outcomes were acceptable in F100 and further improved with experience in S100 Mentoring can minimize the LRP learning curve, and it remains a valid minimally invasive surgical treatment for prostate cancer in Australia even in early practice

7 citations


Authors

Showing all 387 results

NameH-indexPapersCitations
Jennie Ponsford7339318379
Peter J. Stern532358622
Roger Hart461547065
Glynda J. Kinsella401205752
Jacinta Douglas391804737
Gabriela Möslein361126057
Pamela Claire Snow361424496
Michael Denkinger341473214
Thomas Daikeler301413309
John Olver251033189
J. C. Thijs24462194
Daniel Navot24562705
Bernd Sanner231022652
Ulrike Nitz22984068
Dries Testelmans22922100
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20223
202148
202039
201927
201819
201723