dc.contributor.author | Brink, Magnus | |
dc.date.accessioned | 2015-01-07T10:25:18Z | |
dc.date.available | 2015-01-07T10:25:18Z | |
dc.date.issued | 2015-01-07 | |
dc.identifier.isbn | 978-91-628-9189-3 (e-pub) | |
dc.identifier.isbn | 978-91-628-9188-6 (print) | |
dc.identifier.uri | http://hdl.handle.net/2077/37107 | |
dc.description.abstract | Acute bacterial meningitis (ABM), influenza, and necrotizing soft-tissue infections
(NSTIs) are diseases that in a short period of time can progress to become life
threatening. Individuals with severe forms of these infections must be treated in an
intensive care unit were monitoring and support of failing organs improve the
chances of survival. The overall aims of this thesis were to elucidate some aspects of
the clinical presentation, diagnosis and intensive care treatment of ABM, severe
influenza, and NSTIs.
In paper I, we investigated the outcome of 79 episodes of adult ABM. All patients
were given β-lactam antibiotics according to the Swedish tradition with 8-hour
intervals between the doses. This is less frequent compared with recommendations in
most international guidelines. We found a high survival rate (94%), which suggests
that other factors than antibiotic dosing intervals are more important. Streptococcus
pneumoniae was the most common pathogen (48%).
In paper II, we explored the over-time performance for ABM diagnosis with broadrange
polymerase chain reaction and immunochromatographic test. Both tests were
highly sensitive for detection of bacteria in cerebrospinal fluid sampled up to one
week into antibiotic therapy.
In paper III, we investigated the clinical characteristics and outcomes among the
126 Swedish cases of pandemic influenza A (H1N1) that required intensive care
treatment. Risk factors were obesity, chronic pulmonary disease, and diabetes. The
mortality was similar to what has been reported from other comparable countries.
The use of non-invasive ventilation was not associated with improved outcomes
compared with immediate invasive ventilation.
In paper IV, we studied patients with NSTIs treated at Sahlgrenska University
Hospital/East during the period 2008–2011. The 30-day mortality was 14% and the
incidence of amputation 24%. Group A streptococcus was the most common
pathogen followed by Enterobacteriacae and colonic anaerobe bacteria. Inter-hospital
transfer was not associated with a delay in key interventions and could not be
identified as a risk factor for adverse outcome. | sv |
dc.language.iso | eng | sv |
dc.relation.haspart | I. Outcome of 8-hour dosing intervals with beta-lactam antibiotics in adult acute bacterial meningitis.
Brink M, Hagberg L. Scand J Infect Dis. 2006;38(9):772-7.
::PMID::16938730 | sv |
dc.relation.haspart | II. Time window for positive cerebrospinal fluid broad-range bacterial PCR and streptococcus pneumoniae immunochromatographic test in acute bacterial meningitis. Brink M. Welinder-Ohlsson C. Hagberg L. Submitted | sv |
dc.relation.haspart | III. Respiratory support during the influenza A (H1N1) pandemic flu in Sweden.
Brink M, Hagberg L, Larsson A, Gedeborg R.
Acta Anaesthesiol Scand. 2012 Sep;56(8):976-86. Epub 2012 Jun 22.
::PMID::22724889 | sv |
dc.relation.haspart | IV. A series of severe necrotising soft-tissue infections in a regional centre in Sweden.
Brink M, Arnell P, Lycke H, Rosemar A, Hagberg L. Acta Anaesthesiol Scand. 2014 Aug;58(7):882-90. doi: 10.1111/aas.12345. Epub 2014 Jun 13.
::PMID::24924532 | sv |
dc.subject | intensive care | sv |
dc.subject | infection | sv |
dc.subject | acute bacterial meningitis | sv |
dc.subject | beta-lactam antibiotics | sv |
dc.subject | cerebrospinal fluid | sv |
dc.subject | polymerase chain reaction | sv |
dc.subject | immunochromatographic test | sv |
dc.subject | influenza A H1N1 | sv |
dc.subject | pandemic | sv |
dc.subject | non-invasive ventilation | sv |
dc.subject | necrotizing soft-tissue infection | sv |
dc.subject | inter-hospital transfer | sv |
dc.title | On community acquired infections requiring intensive care | sv |
dc.type | text | eng |
dc.type.svep | Doctoral thesis | eng |
dc.gup.mail | magnus.brink@gu.se | sv |
dc.type.degree | Doctor of Philosophy (Medicine) | sv |
dc.gup.origin | University of Gothenburg. Sahlgrenska Academy | sv |
dc.gup.department | Institute of Biomedicine. Department of Infectious Diseases | sv |
dc.gup.defenceplace | Torsdag 15 januari 2015, kl. 13.00, Föreläsningssalen, Infektionskliniken, Sahlgrenska Universitetssjukhuset/Östra | sv |
dc.gup.defencedate | 2015-01-15 | |
dc.gup.dissdb-fakultet | SA | |