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Bronchopneumonia

Inflammation of the lung parenchyma that is associated with BRONCHITIS, usually involving lobular areas from TERMINAL BRONCHIOLES to the PULMONARY ALVEOLI. The affected areas become filled with exudate that forms consolidated patches.
Also Known As:
Bronchial Pneumonia; Bronchial Pneumonias; Bronchopneumonias; Pneumonia, Bronchial; Pneumonias, Bronchial
Networked: 783 relevant articles (51 outcomes, 64 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Infections
2. Bronchitis
3. Urinary Tract Infections (Urinary Tract Infection)
4. Pneumonia (Pneumonitis)
5. Sepsis (Septicemia)

Experts

1. Rouby, Jean-Jacques: 6 articles (01/2022 - 07/2002)
2. Suzuki, Kazuyuki: 4 articles (07/2019 - 07/2008)
3. Giguère, S: 4 articles (01/2017 - 01/2015)
4. Goldstein, Ivan: 4 articles (12/2006 - 07/2002)
5. Fratrić, Natalija: 3 articles (12/2020 - 12/2012)
6. Ilić, Vesna: 3 articles (12/2020 - 12/2012)
7. Caswell, Jeff L: 3 articles (07/2019 - 12/2007)
8. Experimental ICU Study Group: 3 articles (12/2006 - 03/2001)
9. Marquette, Charles-Hugo: 3 articles (05/2005 - 07/2002)
10. Ackermann, Mark R: 3 articles (10/2004 - 09/2002)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Bronchopneumonia:
1. Anti-Bacterial Agents (Antibiotics)IBA
2. Azithromycin (Zithromax)FDA LinkGeneric
3. Ambroxol (Mucosolvan)IBA
4. Meloxicam (Mobic)FDA LinkGeneric
5. Amoxicillin (Wymox)FDA LinkGeneric
6. Rifampin (Rifampicin)FDA LinkGeneric
7. Amoxicillin-Potassium Clavulanate Combination (Co-amoxiclav)FDA Link
8. Biomarkers (Surrogate Marker)IBA
9. FlumethasoneIBA
10. flunixin meglumine (Banamine)IBA

Therapies and Procedures

1. Therapeutics
2. Injections
3. Transplantation
4. Intravenous Administration
11/15/2002 - "After nebulization, AMK lung tissue concentrations were 3- to 30-fold higher than after intravenous administration and were influenced by the severity of lung lesions: 188 +/- 175 microg x g-1 in lung segments with mild bronchopneumonia versus 40 +/- 65 microg x g-1 in lung segments with severe bronchopneumonia (p < 0.01). "
11/01/1979 - "3) Serious upper respiratory tract inflammations, low respiratory tract inflammations (acute bronchitis and bronchopneumonia), staphylococcal exanthema and acute urinary tract infections mostly responded well to CXM intravenous administration (one shot injection, or instillation at dose of 50 approximately mg/kg/day in 2 approximately 3 daily divided doses. "
11/01/1980 - "The results obtained were summarized as follows; 1. Intravenous administration was effective in three cases of pulmonary abscess, in one case of bronchopneumonia, in one case of urinary tract infection complicated to nephrolithiasis, in one case of Mycoplasma pneumonia and in one case of tsutsugamushi disease. "
05/01/2005 - "As compared with intravenous administration, nebulization of ceftazidime significantly increased lung tissue concentrations (17 +/- 13 vs. 383 +/- 84 microg/g in noninfected piglets and 10 +/- 3 vs. 129 +/- 108 microg/g in piglets with experimental bronchopneumonia; P < 0.001). "
07/01/2002 - "In a porcine model of severe bronchopneumonia, the nebulization of amikacin provided 3-30 times higher pulmonary concentrations than the intravenous administration of an equivalent dose. "
5. Artificial Respiration (Mechanical Ventilation)