Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2023A pandemic within a pandemic? Admission to COVID-19 wards in hospitals is associated with increased prevalence of antimicrobial resistance in two African settingscitations

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Chart of shared publication
Mulonga, Kangwa
1 / 1 shared
Adam, Abdelsalam
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Matibula, Peter
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Sikakena, Kapatiso
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Thomason, Margaret J.
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Mohammed, Alaelddin
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Mchugh, Timothy D.
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Elton, Linzy
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Hamid, Muzamil Mahdi Abdel
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Elbadawi, Hana
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Tembo, John
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Nakazwe, Ruth
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Kabaso, Mwewa
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Zumla, Alimuddin
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Fwoloshi, Sombo
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Roulston, Kerry
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Abdelraheem, Mohammed H.
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Maluzi, Kwitaka
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Kabanda, Caren
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Cullip, Teresa
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Honeyborne, Isobella
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2023

Co-Authors (by relevance)

  • Mulonga, Kangwa
  • Adam, Abdelsalam
  • Matibula, Peter
  • Sikakena, Kapatiso
  • Thomason, Margaret J.
  • Mohammed, Alaelddin
  • Mchugh, Timothy D.
  • Elton, Linzy
  • Hamid, Muzamil Mahdi Abdel
  • Elbadawi, Hana
  • Tembo, John
  • Nakazwe, Ruth
  • Kabaso, Mwewa
  • Zumla, Alimuddin
  • Fwoloshi, Sombo
  • Roulston, Kerry
  • Abdelraheem, Mohammed H.
  • Maluzi, Kwitaka
  • Kabanda, Caren
  • Cullip, Teresa
  • Honeyborne, Isobella
OrganizationsLocationPeople

article

A pandemic within a pandemic? Admission to COVID-19 wards in hospitals is associated with increased prevalence of antimicrobial resistance in two African settings

  • Mulonga, Kangwa
  • Adam, Abdelsalam
  • Matibula, Peter
  • Sikakena, Kapatiso
  • Thomason, Margaret J.
  • Mohammed, Alaelddin
  • Mchugh, Timothy D.
  • Elton, Linzy
  • Elhag, Kamal
  • Hamid, Muzamil Mahdi Abdel
  • Elbadawi, Hana
  • Tembo, John
  • Nakazwe, Ruth
  • Kabaso, Mwewa
  • Zumla, Alimuddin
  • Fwoloshi, Sombo
  • Roulston, Kerry
  • Abdelraheem, Mohammed H.
  • Maluzi, Kwitaka
  • Kabanda, Caren
  • Cullip, Teresa
  • Honeyborne, Isobella
Abstract

<jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Patients who develop severe illness due to COVID-19 are more likely to be admitted to hospital and acquire bacterial co-infections, therefore the WHO recommends empiric treatment with antibiotics. Few reports have addressed the impact of COVID-19 management on emergence of nosocomial antimicrobial resistance (AMR) in resource constrained settings. This study aimed to ascertain whether being admitted to a COVID-19 ward (with COVID-19 infection) compared to a non-COVID-19 ward (as a COVID-19 negative patient) was associated with a change in the prevalence of bacterial hospital acquired infection (HAI) species or resistance patterns, and whether there were differences in antimicrobial stewardship (AMS) and infection prevention and control (IPC) guidelines between COVID-19 and non-COVID-19 wards. The study was conducted in Sudan and Zambia, two resource constrained settings with differing country-wide responses to COVID-19.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Patients suspected of having hospital acquired infections were recruited from COVID-19 wards and non-COVID-19 wards. Bacteria were isolated from clinical samples using culture and molecular methods and species identified. Phenotypic and genotypic resistance patterns were determined by antibiotic disc diffusion and whole genome sequencing. Infection prevention and control guidelines were analysed for COVID-19 and non-COVID-19 wards to identify potential differences.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>109 and 66 isolates were collected from Sudan and Zambia respectively. Phenotypic testing revealed significantly more multi-drug resistant isolates on COVID-19 wards in both countries (Sudan <jats:italic>p</jats:italic> = 0.0087, Zambia <jats:italic>p</jats:italic> = 0.0154). The total number of patients with hospital acquired infections (both susceptible and resistant) increased significantly on COVID-19 wards in Sudan, but the opposite was observed in Zambia (both <jats:italic>p</jats:italic> = ≤ 0.0001). Genotypic analysis showed significantly more β-lactam genes per isolate on COVID-19 wards (Sudan <jats:italic>p</jats:italic> = 0.0192, Zambia <jats:italic>p</jats:italic> = ≤ 0.0001).</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Changes in hospital acquired infections and AMR patterns were seen in COVID-19 patients on COVID-19 wards compared to COVID-19 negative patients on non-COVID-19 wards in Sudan and Zambia. These are likely due to a potentially complex combination of causes, including patient factors, but differing emphases on infection prevention and control, and antimicrobial stewardship policies on COVID-19 wards were highlighted.</jats:p></jats:sec>

Topics
  • impedance spectroscopy
  • size-exclusion chromatography
  • additive manufacturing
  • ion-pair chromatography
  • Accelerator mass spectrometry