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The delay before adequate antibiotherapy is known to influence patients' outcome.
2
Therefore it is likely that this re-establishment of protective cellular immunity synergizes with antibiotherapy.
3
Microbiota alterations reverted toward baseline, but were not yet completely restored 2 weeks after antibiotherapy.
4
Prophylactic oral antibiotherapy was given, while hematopoietic growth factors and stem cell support were not employed.
5
Because of diagnostic difficulties and potential mortality in predisposed patients, empirical antibiotherapy has been extensively recommended.
6
We additionally observed that antibiotherapy prevented DLN destruction and lymphocyte depletion, which occurs during untreated experimental infections.
7
Features associated with the antibiotherapy of UTI such as development of resistance are presented in the text systematically.
8
We present herein a new case report in which pseudomembranous colitis was secondary to prophylactic antibiotherapy with pefloxacin for hip prosthesis.
9
As a result the infections caused by resistant bacteria may lead to a high cost of antibiotherapy, prolonged hospitalization duration, and failure of the treatment.
10
A clinical improvement was noted after 1-month antibiotherapy, confirmed by short-term and 6-month imaging follow-up showing the complete disappearance of all previously observed abnormalities.
11
The delay before adequate antibiotherapy is known to influence patients' outcome.
12
Therefore it is likely that this re-establishment of protective cellular immunity synergizes with antibiotherapy.
13
Microbiota alterations reverted toward baseline, but were not yet completely restored 2 weeks after antibiotherapy.
14
Prophylactic oral antibiotherapy was given, while hematopoietic growth factors and stem cell support were not employed.
15
Because of diagnostic difficulties and potential mortality in predisposed patients, empirical antibiotherapy has been extensively recommended.
16
We additionally observed that antibiotherapy prevented DLN destruction and lymphocyte depletion, which occurs during untreated experimental infections.