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trimethoprim and Cystic Fibrosis of Pancreas

trimethoprim has been researched along with Cystic Fibrosis of Pancreas in 27 studies

Trimethoprim: A pyrimidine inhibitor of dihydrofolate reductase, it is an antibacterial related to PYRIMETHAMINE. It is potentiated by SULFONAMIDES and the TRIMETHOPRIM, SULFAMETHOXAZOLE DRUG COMBINATION is the form most often used. It is sometimes used alone as an antimalarial. TRIMETHOPRIM RESISTANCE has been reported.
trimethoprim : An aminopyrimidine antibiotic whose structure consists of pyrimidine 2,4-diamine and 1,2,3-trimethoxybenzene moieties linked by a methylene bridge.

Research Excerpts

ExcerptRelevanceReference
"The disposition of sulfamethoxazole and trimethoprim, after constant rate intravenous administration (10 mg/kg/hr sulfamethoxazole and 2 mg/kg/hr trimethoprim for 1 hour), was investigated in adult patients with cystic fibrosis (n = 7) and in age-matched healthy subjects (control subjects, n = 8)."7.68Disposition of drugs in cystic fibrosis. I. Sulfamethoxazole and trimethoprim. ( Hutabarat, RM; McNamara, S; Ramsey, B; Sahajwalla, C; Smith, AL; Unadkat, JD, 1991)
"The first-dose and steady-state pharmacokinetics of trimethoprim and sulfamethoxazole were determined in 14 patients with cystic fibrosis."7.67Dosing implications of rapid elimination of trimethoprim-sulfamethoxazole in patients with cystic fibrosis. ( Bertino, JS; Blumer, JL; Myers, CM; Reed, MD; Stern, RC; Yamashita, TS, 1984)
"During a 1-year period, the prevalence of thymidine-dependent (TD) Staphylococcus aureus in patients at two geographically distinct cystic fibrosis (CF) centers was determined."7.67Prevalence of thymidine-dependent Staphylococcus aureus in patients with cystic fibrosis. ( Gage, PA; Gilligan, PH; Muszynski, MJ; Wait, KR; Welch, DF, 1987)
"The disposition of sulfamethoxazole and trimethoprim, after constant rate intravenous administration (10 mg/kg/hr sulfamethoxazole and 2 mg/kg/hr trimethoprim for 1 hour), was investigated in adult patients with cystic fibrosis (n = 7) and in age-matched healthy subjects (control subjects, n = 8)."3.68Disposition of drugs in cystic fibrosis. I. Sulfamethoxazole and trimethoprim. ( Hutabarat, RM; McNamara, S; Ramsey, B; Sahajwalla, C; Smith, AL; Unadkat, JD, 1991)
"The first-dose and steady-state pharmacokinetics of trimethoprim and sulfamethoxazole were determined in 14 patients with cystic fibrosis."3.67Dosing implications of rapid elimination of trimethoprim-sulfamethoxazole in patients with cystic fibrosis. ( Bertino, JS; Blumer, JL; Myers, CM; Reed, MD; Stern, RC; Yamashita, TS, 1984)
"During a 1-year period, the prevalence of thymidine-dependent (TD) Staphylococcus aureus in patients at two geographically distinct cystic fibrosis (CF) centers was determined."3.67Prevalence of thymidine-dependent Staphylococcus aureus in patients with cystic fibrosis. ( Gage, PA; Gilligan, PH; Muszynski, MJ; Wait, KR; Welch, DF, 1987)
"Ciprofloxacin MICs were 0."1.30In-vitro investigation of the antibacterial activity of agents which may be used for the oral treatment of lung infections in CF patients. ( Hamilton, VE; Richards, RM; Thomas, MR, 1998)
"Inadequate therapeutic results in the treatment of bacterial infections in patients with Cystic Fibrosis prompted a reevaluation of pharmacokinetic parameters of orally and parenterally administered drugs in these patients."1.26[Pharmacokinetic of antibiotics in patients with mucoviscidosis (author's transl)]. ( Guggenbichler, JP; Pillwein, K; Rohrer, R; Schabel, F, 1981)
"The same applies for mucoviscidosis, in which P."1.26[Therapy of chronic respiratory tract infections in children, including mucoviscidosis (author's transl)]. ( Adam, D, 1979)

Research

Studies (27)

TimeframeStudies, this research(%)All Research%
pre-199016 (59.26)18.7374
1990's3 (11.11)18.2507
2000's2 (7.41)29.6817
2010's2 (7.41)24.3611
2020's4 (14.81)2.80

Authors

AuthorsStudies
Chung, WJ1
Goeckeler-Fried, JL1
Havasi, V1
Chiang, A1
Rowe, SM1
Plyler, ZE1
Hong, JS1
Mazur, M1
Piazza, GA1
Keeton, AB1
White, EL1
Rasmussen, L1
Weissman, AM1
Denny, RA1
Brodsky, JL1
Sorscher, EJ1
Chang, TH1
Chuang, YC1
Wang, JT1
Sheng, WH1
Jaiyesimi, OA1
McAvoy, AC2
Fogg, DN1
Garg, N2
Jaiyesimi, O1
Threatt, PH1
Seladi, T1
Goldberg, JB1
da Silva, RR1
Jones, C1
Webster, G1
Mullins, AJ1
Jenner, M1
Bull, MJ1
Dashti, Y1
Spilker, T1
Parkhill, J1
Connor, TR1
LiPuma, JJ1
Challis, GL1
Mahenthiralingam, E1
Van Dalem, A1
Herpol, M1
Echahidi, F1
Peeters, C1
Wybo, I1
De Wachter, E1
Vandamme, P1
Piérard, D1
Tomlin, KL1
Clark, SR1
Ceri, H1
Petersen, BE1
Jenkins, SG1
Yuan, S1
Lamm, C1
Szporn, AH1
Marks, MI1
Gold, R1
Jin, E1
Levison, H1
Isles, A1
Fleming, PC1
Reed, MD1
Stern, RC1
Bertino, JS1
Myers, CM1
Yamashita, TS1
Blumer, JL1
Huang, NN2
Schidlow, DV1
Palmer, JJ1
Antonelli, M1
De Angelis, M1
Bravo, E1
Lorusso, G1
Ascalone, V1
Guggenbichler, JP1
Pillwein, K1
Schabel, F1
Rohrer, R1
Middleton, PG1
Geddes, DM1
Alton, EW1
Richards, RM1
Hamilton, VE1
Thomas, MR1
Sparham, PD1
Lobban, DI1
Speller, DC1
Adam, D1
Hughes, DT1
Pines, A1
Percival, A1
Stille, W1
Quietzsch, J1
Siegert, E1
Günther, J1
Parsons, RL1
Paddock, GM1
Hutabarat, RM1
Unadkat, JD1
Sahajwalla, C1
McNamara, S1
Ramsey, B1
Smith, AL1
Kuriyama, S1
Panosian, C1
Lapointe, JR1
Bourget, C1
Lafleur, L1
Lagacé, J1
Montplaisir, S1
Gilligan, PH1
Gage, PA1
Welch, DF1
Muszynski, MJ1
Wait, KR1
Rawal, BD1
McKay, G1
Blackhall, MI1

Reviews

2 reviews available for trimethoprim and Cystic Fibrosis of Pancreas

ArticleYear
Antibiotics in pediatric respiratory diseases.
    Clinics in chest medicine, 1980, Volume: 1, Issue:3

    Topics: Aminoglycosides; Anti-Bacterial Agents; Cephalosporins; Child; Chloramphenicol; Cystic Fibrosis; Emp

1980
Respiratory pharmacology. Antibiotics. II. Aminoglycosides, polymyxins, vancomycin, trimethoprim-sulfamethoxazole, and pentamidine.
    Clinics in chest medicine, 1986, Volume: 7, Issue:3

    Topics: Aminoglycosides; Anti-Bacterial Agents; Cystic Fibrosis; Drug Combinations; Drug Resistance, Microbi

1986

Other Studies

25 other studies available for trimethoprim and Cystic Fibrosis of Pancreas

ArticleYear
Increasing the Endoplasmic Reticulum Pool of the F508del Allele of the Cystic Fibrosis Transmembrane Conductance Regulator Leads to Greater Folding Correction by Small Molecule Therapeutics.
    PloS one, 2016, Volume: 11, Issue:10

    Topics: Alleles; Benzoates; Cells, Cultured; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regu

2016
Clinical characteristics and outcomes of non-cystic fibrosis patients with Burkholderia cepacia complex bacteremia at a medical center in Taiwan.
    Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi, 2022, Volume: 55, Issue:6 Pt 2

    Topics: Adult; Aged; Anti-Bacterial Agents; Bacteremia; Burkholderia cepacia; Burkholderia cepacia complex;

2022
Metabolomic profiling of Burkholderia cenocepacia in synthetic cystic fibrosis sputum medium reveals nutrient environment-specific production of virulence factors.
    Scientific reports, 2021, 11-01, Volume: 11, Issue:1

    Topics: Anti-Bacterial Agents; Bacterial Proteins; Burkholderia cenocepacia; Burkholderia Infections; Chroma

2021
Differences in Cystic Fibrosis-Associated
    ACS infectious diseases, 2020, 05-08, Volume: 6, Issue:5

    Topics: Anti-Bacterial Agents; Burkholderia; Burkholderia Infections; Cystic Fibrosis; Humans; Metabolome; T

2020
Kill and cure: genomic phylogeny and bioactivity of
    Microbial genomics, 2021, Volume: 7, Issue:1

    Topics: Biosynthetic Pathways; Bongkrekic Acid; Burkholderia gladioli; Cystic Fibrosis; Food Microbiology; H

2021
    Antimicrobial agents and chemotherapy, 2018, Volume: 62, Issue:9

    Topics: Anti-Bacterial Agents; Azabicyclo Compounds; Burkholderia cepacia complex; Ceftazidime; Cephalospori

2018
Green and red fluorescent protein vectors for use in biofilm studies of the intrinsically resistant Burkholderia cepacia complex.
    Journal of microbiological methods, 2004, Volume: 57, Issue:1

    Topics: Anti-Infective Agents; Biofilms; Burkholderia cepacia complex; Cystic Fibrosis; Genetic Vectors; Gre

2004
Nocardia farcinica isolated from bronchoalveolar lavage fluid of a child with cystic fibrosis.
    The Pediatric infectious disease journal, 2007, Volume: 26, Issue:9

    Topics: Anti-Infective Agents; Bronchoalveolar Lavage; Child; Cystic Fibrosis; Drug Combinations; Humans; Ma

2007
Treatment of cystic fibrosis with trimethoprim-sulfamethoxazole.
    The Journal of pediatrics, 1984, Volume: 105, Issue:4

    Topics: Cystic Fibrosis; Drug Combinations; Humans; Sulfamethoxazole; Trimethoprim; Trimethoprim, Sulfametho

1984
Ceftazidime alone and in combination in patients with cystic fibrosis: lack of efficacy in treatment of severe respiratory infections caused by Pseudomonas cepacia.
    The Journal of antimicrobial chemotherapy, 1983, Volume: 12 Suppl A

    Topics: Adolescent; Ceftazidime; Cephalosporins; Cystic Fibrosis; Drug Combinations; Drug Therapy, Combinati

1983
Dosing implications of rapid elimination of trimethoprim-sulfamethoxazole in patients with cystic fibrosis.
    The Journal of pediatrics, 1984, Volume: 104, Issue:2

    Topics: Adolescent; Adult; Cystic Fibrosis; Dose-Response Relationship, Drug; Drug Combinations; Drug Synerg

1984
[Absorption of orally-administered cotrimoxazole in patients with cystic fibrosis].
    Minerva pediatrica, 1982, Nov-15, Volume: 34, Issue:21

    Topics: Child; Child, Preschool; Cystic Fibrosis; Drug Combinations; Humans; Intestinal Absorption; Sulfamet

1982
[Pharmacokinetic of antibiotics in patients with mucoviscidosis (author's transl)].
    Padiatrie und Padologie, 1981, Volume: 16, Issue:4

    Topics: Adolescent; Adult; Anti-Bacterial Agents; Azlocillin; Child; Cystic Fibrosis; Gentamicins; Humans; M

1981
Trimethoprim and tetracycline inhibit airway epithelial sodium absorption.
    American journal of respiratory and critical care medicine, 1996, Volume: 154, Issue:1

    Topics: Absorption; Adult; Amiloride; Animals; Anti-Bacterial Agents; Anti-Infective Agents; Cystic Fibrosis

1996
In-vitro investigation of the antibacterial activity of agents which may be used for the oral treatment of lung infections in CF patients.
    The Journal of antimicrobial chemotherapy, 1998, Volume: 42, Issue:2

    Topics: Administration, Oral; Anti-Bacterial Agents; Ciprofloxacin; Cystic Fibrosis; Drug Therapy, Combinati

1998
Thymidine-requiring Staphylococcus aureus.
    Lancet (London, England), 1978, Jan-14, Volume: 1, Issue:8055

    Topics: Cystic Fibrosis; Drug Resistance, Microbial; Humans; Staphylococcus aureus; Thymidine; Trimethoprim

1978
[Therapy of chronic respiratory tract infections in children, including mucoviscidosis (author's transl)].
    Infection, 1979, Volume: 7 Suppl 6

    Topics: Cephalosporins; Child; Child, Preschool; Cystic Fibrosis; Drug Combinations; Humans; Infant; Infant,

1979
Round table discussion--treatment of lower respiratory tract infections with co-trimoxazole.
    The Journal of antimicrobial chemotherapy, 1979, Volume: 5, Issue:B

    Topics: Bronchiectasis; Bronchitis; Chronic Disease; Cystic Fibrosis; Drug Combinations; Humans; Lung Absces

1979
[Multilobular biliary liver cirrhosis as a purely hepatic form of mucoviscidosis].
    Deutsche Zeitschrift fur Verdauungs- und Stoffwechselkrankheiten, 1979, Volume: 37, Issue:4

    Topics: Child; Cholangitis; Cholecystitis; Cystic Fibrosis; Drug Combinations; Humans; Liver Cirrhosis; Male

1979
The use of new antibiotic agents for chronic pulmonary disease.
    Pediatric annals, 1978, Volume: 7, Issue:1

    Topics: Agammaglobulinemia; Aminoglycosides; Anti-Bacterial Agents; Asthma; Bacterial Infections; Cephalospo

1978
Absorption of two antibacterial drugs, cephalexin and co-trimoxazole, in malabsorption syndromes.
    The Journal of antimicrobial chemotherapy, 1975, Volume: 1, Issue:3 Suppl

    Topics: Celiac Disease; Cephalexin; Cholestyramine Resin; Crohn Disease; Cystic Fibrosis; Diverticulum; Drug

1975
Disposition of drugs in cystic fibrosis. I. Sulfamethoxazole and trimethoprim.
    Clinical pharmacology and therapeutics, 1991, Volume: 49, Issue:4

    Topics: Adult; Chromatography, High Pressure Liquid; Cystic Fibrosis; Female; Humans; Male; Metabolic Cleara

1991
Mucoid and pigmentation characters can be suppressed by non-anti-Pseudomonas aeruginosa antibiotics in cystic fibrosis: a report of promising preliminary results.
    Drugs under experimental and clinical research, 1988, Volume: 14, Issue:8

    Topics: Anti-Bacterial Agents; Cystic Fibrosis; Doxycycline; Drug Combinations; Humans; Leucomycins; Pigment

1988
Prevalence of thymidine-dependent Staphylococcus aureus in patients with cystic fibrosis.
    Journal of clinical microbiology, 1987, Volume: 25, Issue:7

    Topics: Culture Media; Cystic Fibrosis; Drug Combinations; Humans; Respiratory System; Staphylococcus aureus

1987
Inhibition of Pseudomonas aeruginosa by ascorbic acid acting singly and in combination with antimicrobials: in-vitro and in-vivo studies.
    The Medical journal of Australia, 1974, Feb-09, Volume: 1, Issue:6

    Topics: Adolescent; Animals; Anti-Bacterial Agents; Ascorbic Acid; Child; Cystic Fibrosis; Drug Combinations

1974