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1.
Clin Rheumatol ; 36(12): 2743-2750, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28980088

ABSTRACT

The objective of this study is to explore the following: (1) the impact of two different initial doses and cumulative 2-year dose of rituximab (RTX) on drug adherence and predictors of adherence to treatment in rheumatoid arthritis (RA) patients in an observational clinical setting, (2) immunoglobulin levels (IgG/IgM/IgA) during repeated treatment and their relation to infections, and (3) development of anti-rituximab antibodies (ADA). All RA patients receiving RTX from January 2003 to April 2012 at the department were included. The initiating doses were 500 or 1000 mg intravenously days 1 and 15. Drug adherence was estimated using life-table. Baseline predictors of adherence to treatment were analyzed using Cox regression model. Levels of immunoglobulins were measured at treatment initiation and before retreatment. Serum levels of RTX and ADA were measured in 96 patients at 6 months using ELISA. One hundred fifty-three patients were included. Seventy-four (48%) started treatment with 500 and 79 (52%) with 1000 mg. No difference in drug adherence was seen between the different initial or cumulative RTX doses. Methotrexate (MTX) use and low DAS28 at baseline predicted better drug adherence. Ig levels decreased with repeated treatments but low levels were not associated with infections. 11/96 patients had developed ADA at 6 months. Long-term adherence to RTX in RA patient was not influenced by starting- or cumulative 2-year doses. MTX use and low DAS28 at baseline was positively associated with drug adherence. Decreasing Ig levels during treatment were not associated with risk of infections. Development of ADA may influence treatment efficacy and tolerability.


Subject(s)
Antirheumatic Agents/therapeutic use , Immunoglobulins/blood , Infections/etiology , Medication Adherence , Rheumatic Fever/drug therapy , Rituximab/therapeutic use , Antibodies/blood , Antirheumatic Agents/administration & dosage , Antirheumatic Agents/adverse effects , Drug Therapy, Combination , Female , Humans , Male , Methotrexate/therapeutic use , Middle Aged , Rheumatic Fever/blood , Rheumatic Fever/immunology , Rituximab/administration & dosage , Rituximab/adverse effects , Rituximab/immunology , Treatment Outcome
2.
Eur J Endocrinol ; 171(4): 519-26, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25084775

ABSTRACT

OBJECTIVE: The number of studies on the incidence of pituitary adenomas (PAs) is limited. The aim of this study was to evaluate the standardised incidence rate (SIR) of PAs in western Sweden. DESIGN, SUBJECTS AND METHODS: Data from adult patients diagnosed with PAs in 2001-2011, living in the Västra Götaland County, were collected from the Swedish Pituitary Registry (SPR). In addition, medical records on all patients diagnosed with PAs at the six hospitals in the region were reviewed. In total, 592 patients were included in the study.Age-SIR, given as rate/100 000 inhabitants (95% CI), was calculated using the WHO 2000 standard population as a reference. RESULTS: The total SIR for PAs was 3.9/100 000 (3.6-4.3); 3.3/100 000 (2.9-3.7) for men and 4.7/100 000 (4.1-5.3) for women. In men, SIR increased with age, while in women SIR peaked at 25-34 years, mainly due to prolactinomas. Non-functioning PA (NFPA) was the most common PA (54%, 1.8/100 000 (1.6-2.0)) followed by prolactinomas (32%, 1.6/100 000 (1.3-1.9)), acromegaly (9%, 0.35/100 000 (0.25-0.45)), Cushing's disease (4%, 0.18/100 000 (0.11-0.25)) and TSH-producing PA (0.7%, 0.03/100 000 (0.00-0.05)). The proportion of macroadenomas for NFPA was 82%, prolactinomas 37%, GH-producing PA 77%, ACTH-producing PA 28% and TSH-producing PA 100%. The lifetime risk for PAs was 0.27% (0.24-0.31) in men and 0.29% (0.26-0.33) in women. CONCLUSION: This study provides a reliable estimate on the overall incidence of PAs and confirms an increased incidence of PAs compared with studies conducted in the pre-magnetic resonance imaging era. The lower proportion of prolactinomas compared with previous studies is probably explained by the different criteria used.


Subject(s)
Acromegaly/epidemiology , Adenoma/epidemiology , Pituitary ACTH Hypersecretion/epidemiology , Pituitary Neoplasms/epidemiology , Prolactinoma/epidemiology , Acromegaly/etiology , Acromegaly/therapy , Adenoma/complications , Adenoma/therapy , Adult , Age Distribution , Aged , Female , Growth Hormone-Secreting Pituitary Adenoma/epidemiology , Humans , Incidence , Male , Medical Records , Middle Aged , Pituitary ACTH Hypersecretion/etiology , Pituitary ACTH Hypersecretion/therapy , Pituitary Neoplasms/complications , Pituitary Neoplasms/therapy , Prolactinoma/therapy , Registries , Retrospective Studies , Risk , Sex Distribution , Sweden/epidemiology
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