Nahla Elsherbiny

Dr. Nahla Elsherbiny


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2014 in International Journal of Infectious Diseases
Verified
Journal Article
Open access
EHElham Hassan
Elham Hassan
AEAbeer S. Abd El-Rehim
Abeer S. Abd El-Rehim
SHSahar M. Hassany
Sahar M. Hassany
AAAsmaa O. Ahmed
Asmaa O. Ahmed
NENahla Elsherbiny
Nahla Elsherbiny
MMMona H. Mohammed
Mona H. Mohammed
End-stage liver disease (ESLD) is associated with dysregulation of the immune system and increased susceptibility to infections. Although invasive fungal infection (IFI) is a growing public health problem, studies of IFI in ESLD are lacking. The aims of this study were to screen for IFI in ESLD and to assess risk factors and serum interleukin 17 (IL-17) as a marker of the cellular immune response. Both blood and ascitic fluid samples were collected from 46 patients with ESLD for fungal culture and PCR. Serum IL-17 levels were determined. Seven patients had isolated IFI (four had spontaneous fungal peritonitis, two had fungemia, and one had a disseminated fungal infection) and five cases had combined fungal and bacterial infections. Spontaneous fungal peritonitis was attributed to Candida species, while fungemia was caused by Aspergillus species. Patients with IFI had higher serum IL-17 levels and increased mortality compared to patients without IFI. A history of antibiotic use (p = 0.002), higher model for end-stage liver disease (MELD) scores (p = 0.04), and hepatorenal syndrome (p = 0.006) were risk factors for IFI. Patients with ESLD had a low frequency of IFI; however, in patients with these infections, delayed diagnosis and treatment may contribute to a high fatality rate. Thus, clinicians should have a high index of suspicion for this unusual but lethal entity, as prompt detection and appropriate treatment can improve the outcome.

6 July 2020 in Microorganisms
Verified
Journal Article
Open access
PDF file
NENahla Elsherbiny
Nahla Elsherbiny
MRMohammed Ramadan
Mohammed Ramadan
EHElham Hassan
Elham Hassan
MAMohamed Ali
Mohamed Ali
AEAbeer S. Abd El-Rehim
Abeer S. Abd El-Rehim
Helal HettaHelal Hetta
Helal Hetta
Autoimmune hepatitis (AIH) is a chronic inflammatory disorder with complex immunopathogenesis. Dysbiosis has been linked to many autoimmune diseases, but its detailed role in autoimmune hepatitis (AIH) still needs rigorous evaluation, especially in Egypt. We aimed to identify the shift in the gut microbiota profile and resultant metabolic pathways in AIH Egyptian patients compared to healthy individuals. Stool samples were collected from 15 AIH-naive patients and from 10 healthy individuals. The V3-V4 hyper-variable regions in16S rRNA gene was amplified and sequenced using Illumina MiSeq platform. Significantly lower bacterial diversity in AIH patients was found compared to the controls. A phylum-level analysis showed the overrepresentation of Firmicutes, Bacteroides, and Proteobacteria. At the genus level, AIH-associated enrichment of Faecalibacterium, Blautia, Streptococcus, Haemophilus, Bacteroides, Veillonella, Eubacterium, Lachnospiraceae and Butyricicoccus was reported in contrast to Prevotella, Parabacteroides and Dilaster, which were significantly retracted in such patients. Overall, the predicted metabolic pathways associated with dysbiosis in AIH patients could orchestrate the potential pathogenic roles of gut microbiota in autoimmune disease, though not in a disease-specific manner, calling for future large-scale studies.

1 September 2012 in Arab Journal of Gastroenterology
Verified
Journal Article
Closed access
NMNadia A. Mohamed
Nadia A. Mohamed
ESEman M. Swify
Eman M. Swify
NANabila F. Amin
Nabila F. Amin
MSMona M. Soliman
Mona M. Soliman
LTLubna M. Tag-Eldin
Lubna M. Tag-Eldin
NENahla Elsherbiny
Nahla Elsherbiny

1 January 2014 in Brazilian Journal of Microbiology
Verified
Journal Article
Open access
PDF file
EDEnas Daef
Enas Daef
AMAhmed Moharram
Ahmed Moharram
SESalwa Seif Eldin
Salwa Seif Eldin
NENahla Elsherbiny
Nahla Elsherbiny
MMMona Mohammed
Mona Mohammed
Identification of Candida cultured from various clinical specimens to the species level is increasingly necessary for clinical laboratories. Although sn PCR identifies the species within hours but its cost-effectiveness is to be considered. So there is always a need for media which help in the isolation and identification at the species level. The study aimed to evaluate the performance of different chromogenic media and to compare the effectiveness of the traditional phenotypic methods vs. seminested polymerase chain reaction (sn PCR) for identification of Candida species. One hundred and twenty seven Candida strains isolated from various clinical specimens were identified by conventional methods, four different chromogenic media and sn PCR. HiCrome Candida Differential and CHROMagar Candida media showed comparably high sensitivities and specificities in the identification of C. albicans, C. tropicalis, C. glabrata and C. krusei. CHROMagar Candida had an extra advantage of identifying all C. parapsilosis isolates. CHROMagar-Pal's medium identified C. albicans, C. tropicalis and C. krusei with high sensitivities and specificities, but couldn't identify C. glabrata or C. parapsilosis. It was the only medium that identified C. dubliniensis with a sensitivity and specificity of 100%. Biggy agar showed the least sensitivities and specificities. The overall concordance of the snPCR compared to the conventional tests including CHROMAgar Candida in the identification of Candida species was 97.5%. The use of CHROMAgar Candida medium is an easy and accurate method for presumptive identification of the most commonly encountered Candida spp.

1 May 2018 in Journal of Infection and Public Health
Verified
Journal Article
Open access
EHElham Hassan
Elham Hassan
NENahla Elsherbiny
Nahla Elsherbiny
AEAbeer S. Abd El-Rehim
Abeer S. Abd El-Rehim
ASAsmaa M.A. Soliman
Asmaa M.A. Soliman
AAAsmaa O. Ahmed
Asmaa O. Ahmed
Background: Health care-associated infections (HAIs) threaten patient's safety worldwide especially in the intensive care units (ICU). In end-stage liver disease (ESLD), the condition is much more complicated. Data regarding HAIs among ESLD patients is lacking. We aimed to assess the incidence of HAIs, risk factors, causative micro-organisms, antimicrobial susceptibilities and mortality rates among patients with end-stage liver disease (ESLD) admitted to pre-transplant liver intensive care unit (LICU). Method: This prospective observational study included 337 ESLD patients admitted to LICU, Al-Rajhi liver center, Assiut University Hospital, Assiut, Egypt between January 2016 and June 2016 and they were followed up for the development of HAI manifestations. The medical history, physical examination and severity of underlying disease were determined. Clinical samples were taken from patients who developed HAIs for microbiological diagnosis and antimicrobial susceptibility testing. Results: A total of 57 (16.9%) ESLD patients developed HAIs with the incidence density of 26.8 per 1000 patient-days. Blood stream infection was the most common (49.1%). Escherichia coli (21.1%) followed by methicillin-resistant Staphylococcus aureus (MRSA) (15.8%) were the commonest bacteria. Multidrug resistant organisms were reported in 52.6% of the isolates. Fungal causes were 15.8% with Candida species dominance. Sphingomonas paucimobilis and Achromobacter dentrificans were reported for the first time as pathogens for HAIs in LICU. Prolonged hospital stay, intravenous line duration, prolonged use of proton pump inhibitors and paracentesis were predictors for HAIs. No significant difference between ESLD patients with and without HAIs regarding mortality (36.8% vs. 48.6%, P = 0.2). Conclusion: High HAI rate among ESLD patients is a matter of worry. Effective surveillance program, active infection control measures and national antibiotic policies are necessary to reduce the burden of HAIs. (C) 2018 The Authors. Published by Elsevier Limited on behalf of King Saud Bin Abdulaziz University for Health Sciences.

2 November 2012 in Journal of Parasitic Diseases
Verified
Journal Article
Closed access
PDF file
MAMona A. Almushait
Mona A. Almushait
SDSaad M. Bin Dajem
Saad M. Bin Dajem
NENahla Elsherbiny
Nahla Elsherbiny
MEMamdoh A. Eskandar
Mamdoh A. Eskandar
TATarik A. Al Azraqi
Tarik A. Al Azraqi
LMLaila M. Makhlouf
Laila M. Makhlouf