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Articles de revues sur le sujet « Theophylline »

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Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 7 septembre 2023

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1

Tatsis, G., J. Danos, M. Gaga, D. Pantelakis, M. Veslemes et J. Jordanoglou. « A Single-Blind Crossover Study of Two Different Slow Release Theophylline Preparations ». Journal of International Medical Research 16, n^o 6 (novembre 1988) : 452–58. http://dx.doi.org/10.1177/030006058801600607.

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In a single-blind crossover study, two slow release theophylline preparations were evaluated in 18 patients with chronic bronchitis or asthma without cardiac, renal or liver disease. After randomization into two groups, patients were treated, in a crossover study design, with 600 mg choline theophyllinate or 300 mg anhydrous theophylline administered orally every 12 h for 7 days. A 2-day washout period separated the two periods of treatment evaluation. Blood samples in which plasma theophylline concentration was to be measured were taken at 7.30 a.m., 2.00 p.m. and 7.30 p.m. during the last 5 days of therapy with each drug. The mean fluctuation in plasma theophylline concentration was ≤40% in all 18 patients taking choline theophyllinate yet in only 15 (83%) patients administered anhydrous theophylline. Salbutamol inhaler was more frequently required for the relief of bronchospasm when taking anhydrous theophylline than when taking choline theophyllinate (total of 41 vs 25 puffs, respectively, over 7 days). Drug-related adverse reactions occurred in four patients while taking anhydrous theophylline and in one patient while taking choline theophyllinate.

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2

Boner, A. L., G. De Stefano, G. Vallone, M. Plebani et P. Ventura. « Absolute and Relative Bioavailability of a Slow Release Theophylline Preparation in Asthmatic Children ». Journal of International Medical Research 15, n^o 5 (septembre 1987) : 282–92. http://dx.doi.org/10.1177/030006058701500504.

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This study was carried out on 14 asthmatic childen aged 7–13 years. They all received three preparations (aminophylline by intravenous infusion, lysine theophyllinate orally in solution and slow release theophylline orally as capsules) in a single dose of 100 mg active ingredient in a crossover design. Plasma theophylline concentrations, determined by a fluorescent polarization immunoassay, were evaluated both by compartmental and non-compartmental analysis. After administration of slow release theophylline, its maximum plasma concentration and the time needed to reach this were (± SD) 3.19 ± 0.63 μg/ml and 8.71 ± 2.30 h, respectively, compared to 4.51 ± 0.94 μg/ml and 1.96 ± 0.85 h, respectively, for the oral normal release solution. Mean absolute and relative percentage bioavailabilities for slow release theophylline in asthmatic children were (± SD) 92.7 ± 23.2% and 83.14 ± 14.69%, respectively. These are similar to the values found with other slow release formulations in paediatric patients.

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3

BRODWALL, ERLING K. « The Resorption of Theophyllamine (Theophylline Ethylenediamine) ». Acta Medica Scandinavica 146, n^o 2 (24 avril 2009) : 123–26. http://dx.doi.org/10.1111/j.0954-6820.1953.tb10222.x.

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4

Nolte, Matthias, Ingo Pantenburg et Gerd Meyer. « Konkurrierende Liganden : Theophyllin als nicht- und stark koordinierender Ligand in Quecksilber(II)-Komplexen / Competing Ligands : Theophylline as Non- and Strongly Coordinating Ligand in Mercury(II) Complexes ». Zeitschrift für Naturforschung B 61, n^o 6 (1 juin 2006) : 758–65. http://dx.doi.org/10.1515/znb-2006-0617.

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[{Hg(CF3)2}(ThpH)(H2O)](H2O) (1), [{Hg4(Thp)4}(ClO4)4(H2O)8](H2O)4 (2), [{Hg(ThpH)2} (NO3)](NO3) (3) and {Hg(Thp)Cl}(H2O) (4) (ThpH = theophylline, C7H8N4O2) have been synthesized by slow evaporation of aqueous solutions of the mercuric salts Hg(CF3)2, Hg(ClO4)2, Hg(NO3)2, or HgCl2 and theophylline. Their crystal structures were determined on the basis of single crystal X-ray data. The coordination polymers 1 and 2 crystallize with triclinic symmetry, P1̅ (no. 2), with a = 468.8(2), b = 1256.4(5), c = 1445.5(6) pm, α = 67.15(3), β = 89.21(3), γ = 89.40(3)° and a = 833.6(1), b = 1862.7(2), c = 2182.9(2) pm, α = 111.61(1), β = 90.98(1), γ = 95.51(1)°, respectively. 3 and 4 crystallize with monoclinic symmetry, Pc (no. 7), a =1194.1(1), b=1258.8(2), c=735.5(2) pm, β =96.96(2)° and P21/n (no. 14), a=1069.0(2), b =911.6(1), c=1089.9(2) pm and β = 96.87(2)°. In 1 the theophylline molecules are non-coordinating to mercury and leave the Hg(CF3)2 molecule unchanged. Only weak electrostatic attractions to one keto-oxygen atom of theophylline and one water molecule hold this co-crystallisate together. In 2, the theophyllinate anion, Thp−, strongly coordinates with both N(7) and N(9) to HgII forming a large ring with eight Hg atoms that incorporates the water molecules. One sort of nitrate ions in 3 is weakly attached to HgII with the theophylline molecules still bound strongly through N(9). The chloride ligand and the theophyllinate ion seem to have the same strengths as ligands in 4 as they are both attached to HgII with the shortest distances possible

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5

Wang, L. C., S. F. Man et A. N. Belcastro. « Metabolic and hormonal responses in theophylline-increased cold resistance in males ». Journal of Applied Physiology 63, n^o 2 (1 août 1987) : 589–96. http://dx.doi.org/10.1152/jappl.1987.63.2.589.

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The effects of theophylline (a phosphodiesterase inhibitor-adenosine receptor antagonist) and substrate feeding (Ensure, 250 kcal/235 ml) on cold resistance were studied in seminude males undertaking submaximal (50% maximum O2 consumption), intermittent (34% of total time) exercise in the cold (-5 to 15 degrees C, individually adjusted) for 3 h. Each subject (n = 7) served as his own control and was tested on a weekly schedule. Under control treatment, rectal temperature (Tre) decreased by 0.9 degrees C to approximately 36.2 degrees C after cold exposure, whereas under theophylline and Ensure, the decrease of Tre was only 0.4 degrees C, indicating a significant increase (P less than 0.05) in cold resistance (50% better than control). The plasma concentration of theophylline was 4.8–5.9 micrograms/ml and was positively correlated with plasma concentration of free fatty acids. Plasma norepinephrine (NE) increased significantly during cold exposure; the absolute concentration was significantly higher after theophylline pretreatment. The plasma concentrations of glucose, epinephrine, cortisol, and adenosine 3′,5′-cyclic monophosphate did not change and the changes of free thyroxine and triiodothyronine were minor. Together, the effectiveness of theophylline + Ensure in acutely increasing cold resistance may be due to increased substrate availability for thermogenesis, part of which, through theophylline's potentiation of both sympathetic release of NE and NE-stimulated lipolysis and part of which, through supplementary feeding of Ensure.

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6

Jeong, Chan Su, Soon Chul Hwang, Daniel W. Jones, Hwan Sun Ryu, Kieho Sohn et Charles D. Sands. « Theophylline Disposition in Korean Patients with Congestive Heart Failure ». Annals of Pharmacotherapy 28, n^o 3 (mars 1994) : 396–401. http://dx.doi.org/10.1177/106002809402800319.

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OBJECTIVE: This study proposed to determine the systemic disposition on of theophyllinein Korean adult patients during decompensated congestive heart failure compared with disposition after recovery. DESIGN: An experimental, prospective, self-controlled, non randomized design was used. SETTING: The study was performed in a general communityhospital located in Pusan, Korea. PATIENTS: Eight nonsmoking elderly Korean patients with decompensated congestive heart failure presenting to the emergency department were included in the study. Consecutive patients who met entrance criteria were selected. All patients completed the study. INTERVENTIONS: A single dose of aminophylline 6 mg/kg was administered by intravenous infusion over 30 minutes. Standard methods of congestive heart failure therapy were used in each patient, including bed rest, restriction of sodium, and drug therapy including digoxin. After compensation of congestive heart failure was achieved the theophylline infusion was repeated. OUTCOME MEASURES: Serum theophylline concentrations were measured at 2, 6, 12, and 18 hours after completion of the dose at base line and following treatment. RESULTS: A clinically and statistically significant improvement in mean theophylline total body clearance was demonstrated following treatment (from 21.7 ± 2.8 to 43.4 ± 4.7 mL/kg/h [mean ± SEM]; p<0.01). Comparison of these results with a computer model based on literature averages of peoples of all nationalities showed significant underprediction of theophylline clearance both before (p<0.05)and after (p<0.01) treatment. The theophylline elimination half-life prior to treatment was 18.2 ± 2.2 hours and decreased to 9.1 ± 0.8 hours following treatment(p<0.O1). There was no statistical difference between the computer-model predicted initial theophylline half-life and the measured value, but the model significantly underpredicted the improvement following treatment. CONCLUSIONS: The improvement in theophylline clearance demonstrated in this study appears to be greater than that reported for Western patients. This has practical application to the calculation of appropriate theophylline maintenance dosage regimens in Korean patients with cardiac failure. These data support the need for consideration of racial differences in individualizing dosage regimens. We suggest that all kinetic models, whether software supported or not, should consider incorporating ethnic origin as a demographic factor that helps select the proper model for individual patients.

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7

Rees, Sharon. « THEOPHYLLINE ». Journal of Prescribing Practice 3, n^o 2 (2 février 2021) : 52. http://dx.doi.org/10.12968/jprp.2021.3.2.52.

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8

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 728 (novembre 1998) : 12. http://dx.doi.org/10.2165/00128415-199807280-00041.

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9

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 1167 (septembre 2007) : 26. http://dx.doi.org/10.2165/00128415-200711670-00078.

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10

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 1152 (mai 2007) : 25–26. http://dx.doi.org/10.2165/00128415-200711520-00078.

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11

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 1371 (octobre 2011) : 35–36. http://dx.doi.org/10.2165/00128415-201113710-00130.

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12

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 533 (janvier 1995) : 11. http://dx.doi.org/10.2165/00128415-199505330-00042.

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13

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 544 (avril 1995) : 12. http://dx.doi.org/10.2165/00128415-199505440-00035.

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14

Napier‐Flood, Fiona E., et Brian R. Creese. « Theophylline ». Medical Journal of Australia 162, n^o 10 (mai 1995) : 548–50. http://dx.doi.org/10.5694/j.1326-5377.1995.tb138519.x.

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15

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 433 (janvier 1993) : 11. http://dx.doi.org/10.2165/00128415-199304330-00048.

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16

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 446 (avril 1993) : 12. http://dx.doi.org/10.2165/00128415-199304460-00053.

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17

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 452 (mai 1993) : 11. http://dx.doi.org/10.2165/00128415-199304520-00051.

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18

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 458 (juillet 1993) : 11. http://dx.doi.org/10.2165/00128415-199304580-00057.

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19

Barnes, Peter J. « Theophylline ». Pharmaceuticals 3, n^o 3 (18 mars 2010) : 725–47. http://dx.doi.org/10.3390/ph3030725.

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20

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 621 (octobre 1996) : 12. http://dx.doi.org/10.2165/00128415-199606210-00041.

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21

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 627 (novembre 1996) : 12. http://dx.doi.org/10.2165/00128415-199606270-00036.

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22

Weinberger, Miles M. « Theophylline ». Immunology and Allergy Clinics of North America 10, n^o 3 (août 1990) : 559–76. http://dx.doi.org/10.1016/s0889-8561(22)00295-8.

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23

Milgrom, Henry. « THEOPHYLLINE ». Immunology and Allergy Clinics of North America 13, n^o 4 (novembre 1993) : 819–38. http://dx.doi.org/10.1016/s0889-8561(22)00662-2.

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24

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 791 (mars 2000) : 12. http://dx.doi.org/10.2165/00128415-200007910-00029.

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25

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 369 (septembre 1991) : 11. http://dx.doi.org/10.2165/00128415-199103690-00060.

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26

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 371 (octobre 1991) : 12. http://dx.doi.org/10.2165/00128415-199103710-00061.

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27

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 374 (octobre 1991) : 8. http://dx.doi.org/10.2165/00128415-199103740-00042.

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28

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 380 (décembre 1991) : 8. http://dx.doi.org/10.2165/00128415-199103800-00041.

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29

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 384 (janvier 1992) : 12. http://dx.doi.org/10.2165/00128415-199203840-00065.

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30

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 403 (mai 1992) : 8. http://dx.doi.org/10.2165/00128415-199204030-00034.

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31

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 1199 (avril 2008) : 44. http://dx.doi.org/10.2165/00128415-200811990-00134.

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32

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 1214 (août 2008) : 29. http://dx.doi.org/10.2165/00128415-200812140-00084.

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33

Markham, Anthony, et Diana Faulds. « Theophylline ». Drugs 56, n^o 6 (1998) : 1081–91. http://dx.doi.org/10.2165/00003495-199856060-00018.

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34

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 915 (août 2002) : 12. http://dx.doi.org/10.2165/00128415-200209150-00040.

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35

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 296 (avril 1990) : 7. http://dx.doi.org/10.2165/00128415-199002960-00032.

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36

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 307 (juin 1990) : 7. http://dx.doi.org/10.2165/00128415-199003070-00034.

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37

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 313 (août 1990) : 8. http://dx.doi.org/10.2165/00128415-199003130-00042.

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38

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 328 (novembre 1990) : 11. http://dx.doi.org/10.2165/00128415-199003280-00059.

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39

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 341 (mars 1991) : 11. http://dx.doi.org/10.2165/00128415-199103410-00067.

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40

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 347 (avril 1991) : 7. http://dx.doi.org/10.2165/00128415-199103470-00033.

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41

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 356 (juin 1991) : 8. http://dx.doi.org/10.2165/00128415-199103560-00037.

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42

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 359 (juillet 1991) : 8. http://dx.doi.org/10.2165/00128415-199103590-00042.

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43

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 364 (août 1991) : 12. http://dx.doi.org/10.2165/00128415-199103640-00058.

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44

Nasser, Shuaib S. M., et P. John Rees. « Theophylline ». Drug Safety 8, n^o 1 (janvier 1993) : 12–18. http://dx.doi.org/10.2165/00002018-199308010-00003.

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45

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 506 (juin 1994) : 12. http://dx.doi.org/10.2165/00128415-199405060-00063.

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46

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 510 (juillet 1994) : 12. http://dx.doi.org/10.2165/00128415-199405100-00056.

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47

&NA;. « Theophylline ». Reactions Weekly &NA;, n^o 1334 (janvier 2011) : 43. http://dx.doi.org/10.2165/00128415-201113340-00153.

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48

Svedmyr, Nils. « Theophylline ». American Review of Respiratory Disease 136, n^o 4_pt_2 (octobre 1987) : S68—S71. http://dx.doi.org/10.1164/ajrccm/136.4_pt_2.s68.

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49

Barnes, Peter J. « Theophylline ». American Journal of Respiratory and Critical Care Medicine 188, n^o 8 (15 octobre 2013) : 901–6. http://dx.doi.org/10.1164/rccm.201302-0388pp.

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50

Vale, Allister. « Theophylline ». Medicine 31, n^o 10 (octobre 2003) : 74–75. http://dx.doi.org/10.1383/medc.31.10.74.27816.

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