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Browsing by Author "Daumerie, C. (7003840029)"

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    Antithyroid drugs in Graves’ hyperthyroidism: differences between “block and replace” and “titration” regimes in frequency of euthyroidism and Graves’ orbitopathy during treatment
    (2021)
    Žarković, M. (7003498546)
    ;
    Wiersinga, W. (7101819215)
    ;
    Perros, P. (7006707944)
    ;
    Bartalena, L. (7102317749)
    ;
    Donati, S. (55236626100)
    ;
    Okosieme, O. (6506743718)
    ;
    Morris, D. (16203319800)
    ;
    Fichter, N. (6603189201)
    ;
    Lareida, J. (57199562074)
    ;
    Daumerie, C. (7003840029)
    ;
    Burlacu, M.-C. (23018289900)
    ;
    Kahaly, G.J. (7005506174)
    ;
    Pitz, S. (7003508414)
    ;
    Beleslin, B. (6701355427)
    ;
    Ćirić, J. (6601995819)
    ;
    Ayvaz, G. (6602696412)
    ;
    Konuk, O. (56180435400)
    ;
    Törüner, F.B. (6602398288)
    ;
    Salvi, M. (7006487887)
    ;
    Covelli, D. (26024659100)
    ;
    Curro, N. (23979561200)
    ;
    Hegedüs, L. (7102638527)
    ;
    Brix, T. (15070407400)
    Purpose: Whereas antithyroid drugs (ATD) are the preferred treatment modality for Graves’ hyperthyroidism (GH), there is still controversy about the optimal regimen for delivering ATD. To evaluate whether ‘Block and Replace’ (B + R) and ‘Titration’ (T) regimes are equivalent in terms of frequency of euthyroidism and Graves’ Orbitopathy (GO) during ATD therapy. Methods: A prospective multicentre observational cohort study of 344 patients with GH but no GO at baseline. Patients were treated with ATD for 18 months according to B + R or T regimen in line with their institution’s policy. Results: Baseline characteristics were similar in both groups. In the treatment period between 6 and 18 months thyrotropin (TSH) slightly increased in both groups, but TSH was on average 0.59 mU/L (95% CI 0.27–0.85) lower in the B + R group at all time points (p = 0.026). Serum free thyroxine (FT4) remained stable during the same interval, with a tendency to higher values in the B + R group. The point-prevalence of euthyroidism (TSH and FT4 within their reference ranges) increased with longer duration of ATD in both groups; it was always higher in the T group than in the B + R group: 48 and 24%, respectively, at 6 months, 81 and 58% at 12 months, and 87 and 63% at 18 months (p < 0.002). There were no significant differences between the B + R and T regimens with respect to the fall in thyrotropin binding inhibiting immunoglobulins (TBII) or thyroid peroxidase antibodies (TPO-Ab). GO developed in 15.9% of all patients: 9.1 and 17.8% in B + R group and T group, respectively, (p = 0.096). GO was mild in 13% and moderate-to-severe in 2%. Conclusion: The prevalence of biochemical euthyroidism during treatment with antithyroid drugs is higher during T compared to B + R regimen. De novo development of GO did not differ significantly between the two regimens, although it tended to be higher in the T group. Whether one regimen is clinically more advantageous than the other remains unclear. © 2020, Italian Society of Endocrinology (SIE).
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    Publication
    Antithyroid drugs in Graves’ hyperthyroidism: differences between “block and replace” and “titration” regimes in frequency of euthyroidism and Graves’ orbitopathy during treatment
    (2021)
    Žarković, M. (7003498546)
    ;
    Wiersinga, W. (7101819215)
    ;
    Perros, P. (7006707944)
    ;
    Bartalena, L. (7102317749)
    ;
    Donati, S. (55236626100)
    ;
    Okosieme, O. (6506743718)
    ;
    Morris, D. (16203319800)
    ;
    Fichter, N. (6603189201)
    ;
    Lareida, J. (57199562074)
    ;
    Daumerie, C. (7003840029)
    ;
    Burlacu, M.-C. (23018289900)
    ;
    Kahaly, G.J. (7005506174)
    ;
    Pitz, S. (7003508414)
    ;
    Beleslin, B. (6701355427)
    ;
    Ćirić, J. (6601995819)
    ;
    Ayvaz, G. (6602696412)
    ;
    Konuk, O. (56180435400)
    ;
    Törüner, F.B. (6602398288)
    ;
    Salvi, M. (7006487887)
    ;
    Covelli, D. (26024659100)
    ;
    Curro, N. (23979561200)
    ;
    Hegedüs, L. (7102638527)
    ;
    Brix, T. (15070407400)
    Purpose: Whereas antithyroid drugs (ATD) are the preferred treatment modality for Graves’ hyperthyroidism (GH), there is still controversy about the optimal regimen for delivering ATD. To evaluate whether ‘Block and Replace’ (B + R) and ‘Titration’ (T) regimes are equivalent in terms of frequency of euthyroidism and Graves’ Orbitopathy (GO) during ATD therapy. Methods: A prospective multicentre observational cohort study of 344 patients with GH but no GO at baseline. Patients were treated with ATD for 18 months according to B + R or T regimen in line with their institution’s policy. Results: Baseline characteristics were similar in both groups. In the treatment period between 6 and 18 months thyrotropin (TSH) slightly increased in both groups, but TSH was on average 0.59 mU/L (95% CI 0.27–0.85) lower in the B + R group at all time points (p = 0.026). Serum free thyroxine (FT4) remained stable during the same interval, with a tendency to higher values in the B + R group. The point-prevalence of euthyroidism (TSH and FT4 within their reference ranges) increased with longer duration of ATD in both groups; it was always higher in the T group than in the B + R group: 48 and 24%, respectively, at 6 months, 81 and 58% at 12 months, and 87 and 63% at 18 months (p < 0.002). There were no significant differences between the B + R and T regimens with respect to the fall in thyrotropin binding inhibiting immunoglobulins (TBII) or thyroid peroxidase antibodies (TPO-Ab). GO developed in 15.9% of all patients: 9.1 and 17.8% in B + R group and T group, respectively, (p = 0.096). GO was mild in 13% and moderate-to-severe in 2%. Conclusion: The prevalence of biochemical euthyroidism during treatment with antithyroid drugs is higher during T compared to B + R regimen. De novo development of GO did not differ significantly between the two regimens, although it tended to be higher in the T group. Whether one regimen is clinically more advantageous than the other remains unclear. © 2020, Italian Society of Endocrinology (SIE).
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    Publication
    Asymmetry indicates more severe and active disease in Graves’ orbitopathy: results from a prospective cross-sectional multicentre study
    (2020)
    Perros, P. (7006707944)
    ;
    Žarković, M.P. (7003498546)
    ;
    Panagiotou, G.C. (55362746900)
    ;
    Azzolini, C. (36127411000)
    ;
    Ayvaz, G. (6602696412)
    ;
    Baldeschi, L. (6602585043)
    ;
    Bartalena, L. (7102317749)
    ;
    Boschi, A.M. (7006668224)
    ;
    Nardi, M. (55550143000)
    ;
    Brix, T.H. (15070407400)
    ;
    Covelli, D. (26024659100)
    ;
    Daumerie, C. (7003840029)
    ;
    Eckstein, A.K. (7003932063)
    ;
    Fichter, N. (6603189201)
    ;
    Ćirić, S. (57079927600)
    ;
    Hegedüs, L. (7102638527)
    ;
    Kahaly, G.J. (7005506174)
    ;
    Konuk, O. (56180435400)
    ;
    Lareida, J.J. (57199562074)
    ;
    Okosieme, O.E. (6506743718)
    ;
    Leo, M. (18037556900)
    ;
    Mathiopoulou, L. (15519735200)
    ;
    Clarke, L. (56313122000)
    ;
    Menconi, F. (6603101916)
    ;
    Morris, D.S. (16203319800)
    ;
    Orgiazzi, J. (7006062635)
    ;
    Pitz, S. (7003508414)
    ;
    Salvi, M. (7006487887)
    ;
    Muller, I. (23052085100)
    ;
    Knežević, M. (36192212000)
    ;
    Wiersinga, W.M. (7101819215)
    ;
    Currò, N. (23979561200)
    ;
    Dayan, C.M. (55161416500)
    ;
    Marcocci, C. (7006557829)
    ;
    Marinò, M. (7201365908)
    ;
    Möller, L. (6602822748)
    ;
    Pearce, S.H. (7102959910)
    ;
    Törüner, F. (6602398288)
    ;
    Bernard, M. (7202666194)
    Purpose: Patients with Graves’ orbitopathy can present with asymmetric disease. The aim of this study was to identify clinical characteristics that distinguish asymmetric from unilateral and symmetric Graves’ orbitopathy. Methods: This was a multi-centre study of new referrals to 13 European Group on Graves’ Orbitopathy (EUGOGO) tertiary centres. New patients presenting over a 4 month period with a diagnosis of Graves’ orbitopathy were included. Patient demographics were collected and a clinical examination was performed based on a previously published protocol. Patients were categorized as having asymmetric, symmetric, and unilateral Graves’ orbitopathy. The distribution of clinical characteristics among the three groups was documented. Results: The asymmetric group (n = 83), was older than the symmetric (n = 157) group [mean age 50.9 years (SD 13.9) vs 45.8 (SD 13.5), p = 0.019], had a lower female to male ratio than the symmetric and unilateral (n = 29) groups (1.6 vs 5.0 vs 8.7, p < 0.001), had more active disease than the symmetric and unilateral groups [mean linical Activity Score 3.0 (SD 1.6) vs 1.7 (SD 1.7), p < 0.001 vs 1.3 (SD 1.4), p < 0.001] and significantly more severe disease than the symmetric and unilateral groups, as measured by the Total Eye Score [mean 8.8 (SD 6.6) vs 5.3 (SD 4.4), p < 0.001, vs 2.7 (SD 2.1), p < 0.001]. Conclusion: Older age, lower female to male ratio, more severe, and more active disease cluster around asymmetric Graves’ orbitopathy. Asymmetry appears to be a marker of more severe and more active disease than other presentations. This simple clinical parameter present at first presentation to tertiary centres may be valuable to clinicians who manage such patients. © 2020, The Author(s).
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    Publication
    Asymmetry indicates more severe and active disease in Graves’ orbitopathy: results from a prospective cross-sectional multicentre study
    (2020)
    Perros, P. (7006707944)
    ;
    Žarković, M.P. (7003498546)
    ;
    Panagiotou, G.C. (55362746900)
    ;
    Azzolini, C. (36127411000)
    ;
    Ayvaz, G. (6602696412)
    ;
    Baldeschi, L. (6602585043)
    ;
    Bartalena, L. (7102317749)
    ;
    Boschi, A.M. (7006668224)
    ;
    Nardi, M. (55550143000)
    ;
    Brix, T.H. (15070407400)
    ;
    Covelli, D. (26024659100)
    ;
    Daumerie, C. (7003840029)
    ;
    Eckstein, A.K. (7003932063)
    ;
    Fichter, N. (6603189201)
    ;
    Ćirić, S. (57079927600)
    ;
    Hegedüs, L. (7102638527)
    ;
    Kahaly, G.J. (7005506174)
    ;
    Konuk, O. (56180435400)
    ;
    Lareida, J.J. (57199562074)
    ;
    Okosieme, O.E. (6506743718)
    ;
    Leo, M. (18037556900)
    ;
    Mathiopoulou, L. (15519735200)
    ;
    Clarke, L. (56313122000)
    ;
    Menconi, F. (6603101916)
    ;
    Morris, D.S. (16203319800)
    ;
    Orgiazzi, J. (7006062635)
    ;
    Pitz, S. (7003508414)
    ;
    Salvi, M. (7006487887)
    ;
    Muller, I. (23052085100)
    ;
    Knežević, M. (36192212000)
    ;
    Wiersinga, W.M. (7101819215)
    ;
    Currò, N. (23979561200)
    ;
    Dayan, C.M. (55161416500)
    ;
    Marcocci, C. (7006557829)
    ;
    Marinò, M. (7201365908)
    ;
    Möller, L. (6602822748)
    ;
    Pearce, S.H. (7102959910)
    ;
    Törüner, F. (6602398288)
    ;
    Bernard, M. (7202666194)
    Purpose: Patients with Graves’ orbitopathy can present with asymmetric disease. The aim of this study was to identify clinical characteristics that distinguish asymmetric from unilateral and symmetric Graves’ orbitopathy. Methods: This was a multi-centre study of new referrals to 13 European Group on Graves’ Orbitopathy (EUGOGO) tertiary centres. New patients presenting over a 4 month period with a diagnosis of Graves’ orbitopathy were included. Patient demographics were collected and a clinical examination was performed based on a previously published protocol. Patients were categorized as having asymmetric, symmetric, and unilateral Graves’ orbitopathy. The distribution of clinical characteristics among the three groups was documented. Results: The asymmetric group (n = 83), was older than the symmetric (n = 157) group [mean age 50.9 years (SD 13.9) vs 45.8 (SD 13.5), p = 0.019], had a lower female to male ratio than the symmetric and unilateral (n = 29) groups (1.6 vs 5.0 vs 8.7, p < 0.001), had more active disease than the symmetric and unilateral groups [mean linical Activity Score 3.0 (SD 1.6) vs 1.7 (SD 1.7), p < 0.001 vs 1.3 (SD 1.4), p < 0.001] and significantly more severe disease than the symmetric and unilateral groups, as measured by the Total Eye Score [mean 8.8 (SD 6.6) vs 5.3 (SD 4.4), p < 0.001, vs 2.7 (SD 2.1), p < 0.001]. Conclusion: Older age, lower female to male ratio, more severe, and more active disease cluster around asymmetric Graves’ orbitopathy. Asymmetry appears to be a marker of more severe and more active disease than other presentations. This simple clinical parameter present at first presentation to tertiary centres may be valuable to clinicians who manage such patients. © 2020, The Author(s).

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