Miriam J. Warnier
Utrecht University
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Featured researches published by Miriam J. Warnier.
European Respiratory Journal | 2013
Miriam J. Warnier; Evelien E.S. van Riet; Frans H. Rutten; Marie L. De Bruin; Alfred Sachs
Smoking cessation is the cornerstone of treatment of chronic obstructive pulmonary disease (COPD) patients. This systematic review evaluates the effectiveness of behavioural and pharmacological smoking cessation strategies in COPD patients. MEDLINE was searched from January 2002 to October 2011. Randomised controlled trials evaluating the effect of smoking cessation interventions for COPD patients, published in English, were selected. The methodological quality of included trials was assessed using the Delphi list by two reviewers independently. The relative risks of smoking cessation due to the intervention, compared with controls, were calculated. Eight studies met the inclusion criteria. Heterogeneity was observed for study population, the intervention strategy, the follow-up period and the outcome. According to the Delphi list methodological quality scores, five studies were considered to be of acceptable quality. Pharmacological therapy combined with behavioural counselling was more effective than each strategy separately. In COPD patients, the intensity of counselling did not seem to influence the results, nor did the choice of drug therapy make a difference. This systematic review makes clear that in COPD patients, pharmacological therapy combined with behavioural counselling is more effective than each strategy separately. Neither the intensity of counselling nor the type of anti-smoking drug made a difference.
COPD: Journal of Chronic Obstructive Pulmonary Disease | 2013
Miriam J. Warnier; Frans H. Rutten; Mattijs E. Numans; Jan A. Kors; Hanno L. Tan; Anthonius de Boer; Arno W. Hoes; Marie L. De Bruin
Abstract Patients with chronic obstructive pulmonary disease (COPD) are at increased risk of cardiovascular disease. Electrocardiography (ECG) carries information about cardiac disease and prognosis, but studies comparing ECG characteristics between patients with and without COPD are lacking. We related ECG characteristics of patients with COPD, to ECG characteristics of patients without COPD, and determined whether ECG abnormalities are related to COPD severity. A cross-sectional study was conducted within a cohort of 243 COPD patients, aged 65 years or older. All patients underwent extensive examinations, including resting 12-lead ECG and pulmonary function tests. The reference group (n = 293) was a sample from the general population, also aged 65 or older, without COPD. Abnormal ECGs were more prevalent in COPD patients (50%) than in patients without COPD (36%, p = 0.054). Conduction abnormalities were the most common ECG abnormality in COPD patients (28%) being significantly more prevalent than in patients without COPD (11%, p < 0.001). The mean heart rate was higher in COPD patients (72 bpm (SD 14)) compared to controls (65 bpm (SD 13), p < 0.001), and QTc prolongation was less frequent in COPD patients (9% versus 14%, p = 0.01). The prevalence of ECG abnormalities increased with severity of pulmonary obstruction. ECG abnormalities, especially conduction abnormalities are common in COPD patients, and the prevalence of ECG abnormalities increases with severity of COPD. This underlines the importance of an integrated-care approach for COPD patients, paying attention to early detection of unrecognized coexisting cardiac disorders.
PLOS ONE | 2013
Miriam J. Warnier; Marieke T. Blom; Abdennasser Bardai; Jocelyn Berdowksi; Patrick C. Souverein; Arno W. Hoes; Frans H. Rutten; Anthonius de Boer; Rudolph W. Koster; Marie L. De Bruin; Han Liong Tan
Background We aimed to determine whether (1) patients with obstructive pulmonary disease (OPD) have an increased risk of sudden cardiac arrest (SCA) due to ventricular tachycardia or fibrillation (VT/VF), and (2) the SCA risk is mediated by cardiovascular risk-profile and/or respiratory drug use. Methods A community-based case-control study was performed, with 1310 cases of SCA of the ARREST study and 5793 age, sex and SCA-date matched non-SCA controls from the PHARMO database. Only incident SCA cases, age older than 40 years, that resulted from unequivocal cardiac causes with electrocardiographic documentation of VT/VF were included. Conditional logistic regression analysis was used to assess the association between SCA and OPD. Pre-specified subgroup analyses were performed regarding age, sex, cardiovascular risk-profile, disease severity, and current use of respiratory drugs. Results A higher risk of SCA was observed in patients with OPD (n = 190 cases [15%], 622 controls [11%]) than in those without OPD (OR adjusted for cardiovascular risk-profile 1.4 [1.2–1.6]). In OPD patients with a high cardiovascular risk-profile (OR 3.5 [2.7–4.4]) a higher risk of SCA was observed than in those with a low cardiovascular risk-profile (OR 1.3 [0.9–1.9]) The observed SCA risk was highest among OPD patients who received short-acting β2-adrenoreceptor agonists (SABA) or anticholinergics (AC) at the time of SCA (SABA OR: 3.9 [1.7–8.8], AC OR: 2.7 [1.5–4.8] compared to those without OPD). Conclusions OPD is associated with an increased observed risk of SCA. The most increased risk was observed in patients with a high cardiovascular risk-profile, and in those who received SABA and, possibly, those who received AC at the time of SCA.
The Journal of Clinical Psychiatry | 2014
Ingrid M. M. van Haelst; Wilton A. van Klei; Hieronymus J. Doodeman; Miriam J. Warnier; Marie L. De Bruin; Cor J. Kalkman; Toine C. G. Egberts
OBJECTIVE To investigate the association between the use of a selective serotonin reuptake inhibitor (SSRI) and the occurrence of QT interval prolongation in an elderly surgical population. METHOD A cross-sectional study was conducted among patients (> 60 years) scheduled for outpatient preanesthesia evaluation in the period 2007 until 2012. The index group included elderly users of an SSRI. The reference group of nonusers of antidepressants was matched to the index group on sex and year of scheduled surgery (ratio, 1:1). The primary outcome was the occurrence of QT interval prolongation shown on electrocardiogram. The QT interval was corrected for heart rate (QTc interval). The secondary outcome was the duration of the QTc interval. The outcomes were adjusted for confounding by using regression techniques. RESULTS The index and reference groups included 397 users of an SSRI and 397 nonusers, respectively. QTc interval prolongation occurred in 25 (6%) and 19 (5%) index and reference patients, respectively. After adjustment for confounding, users of an SSRI did not have a higher risk for QTc interval prolongation compared to nonusers: OR = 1.1 (95% CI, 0.5 to 2.0). The adjusted mean QTc interval length in users of an SSRI and nonusers was comparable (difference of 1.5 milliseconds [95% CI, -1.8 to 4.8]). Use of the most frequently used SSRIs citalopram and paroxetine was not associated with a higher risk of QTc interval prolongation nor with lengthening of the QTc interval duration. CONCLUSIONS The use of an SSRI by elderly surgical patients was not associated with the occurrence of QT interval prolongation.
Resuscitation | 2013
Marieke T. Blom; Miriam J. Warnier; Abdennasser Bardai; Jocelyn Berdowski; Rudolph W. Koster; Patrick C. Souverein; Arno W. Hoes; Frans H. Rutten; A. de Boer; M. L. De Bruin; Hanno L. Tan
AIM Out-of-hospital cardiac arrest (OHCA) due to sustained ventricular tachycardia/fibrillation (VT/VF) is common and often lethal. Patients co-morbidities may determine survival after OHCA, and be instrumental in post-resuscitation care, but are poorly studied. We aimed to study whether patients with obstructive pulmonary disease (OPD) have a lower survival rate after OHCA than non-OPD patients. METHODS We performed a community-based cohort study of 1172 patients with non-traumatic OHCA with ECG-documented VT/VF between 2005 and 2008. We compared survival to emergency room (ER), to hospital admission, to hospital discharge, and at 30 days after OHCA, of OPD-patients and non-OPD patients, using logistic regression analysis. We also compared 30-day survival of patients who were admitted to hospital, using multivariate logistic regression analysis. RESULTS OPD patients (n=178) and non-OPD patients (n=994) had comparable survival to ER (75% vs. 78%, OR 0.9 [95% CI: 0.6-1.3]) and to hospital admission (56% vs. 57%, OR 1.0 [0.7-1.4]). However, survival to hospital discharge was significantly lower among OPD patients (21% vs. 33%, OR 0.6 [0.4-0.9]). Multivariate regression analysis among patients who were admitted to hospital (OPD: n=100, no OPD: n=561) revealed that OPD was an independent determinant of reduced 30-day survival rate (39% vs. 59%, adjusted OR 0.6 [0.4-1.0, p=0.035]). CONCLUSION OPD-patients had lower survival rates after OHCA than non-OPD patients. Survival to ER and to hospital admission was not different between both groups. However, among OHCA victims who survived to hospital admission, OPD was an independent determinant of reduced 30-day survival rate.
Journal of Asthma | 2012
Miriam J. Warnier; Frans H. Rutten; Jan A. Kors; Jan Willem J. Lammers; Anthonius de Boer; Arno W. Hoes; Marie L. De Bruin
Objective. The pathogenesis of cardiac arrhythmias in asthma patients has not been fully elucidated. Adverse drug effects, particularly those of β2-mimetics, may play a role. The aim of this study was to determine whether asthma is associated with the risk of cardiac arrhythmias and electrocardiographic characteristics of arrhythmogenicity (ECG) and to explore the role of β2-mimetics. Methods. A cross-sectional study was conducted among 158 adult patients with a diagnosis of asthma and 6303 participants without asthma from the cohort of the Utrecht Health Project—an ongoing, longitudinal, primary care-based study. All patients underwent extensive examinations, including resting 12-lead electrocardiogram (ECG) and pulmonary function tests. The primary outcome was “any arrhythmia on the ECG” (including tachycardia, bradycardia, premature ventricular contraction (PVC), and atrial fibrillation or flutter). Secondary outcomes were tachycardia, bradycardia, PVC, atrial fibrillation or flutter, mean heart rate, mean corrected QT (QTc) interval length, and prolonged QTc interval. Results. Tachycardia and PVCs were more prevalent in patients with asthma (3% and 4%, respectively) than those without asthma (0.6%, p < .001; 2%, p = .03, respectively). The prevalence of QTc interval prolongation was similar in participants with (2%) and without asthma (3%, odds ratio [OR]: 0.6 and 95% confidence interval [95% CI]: 0.2–2.0). In 74 asthma patients, who received β2-mimetics, tachycardia and PVCs were more common (OR: 12.4 [95% CI: 4.7–32.8] and 3.7 [95% CI: 1.3–10.5], respectively). Conclusions. The adult patients with asthma more commonly show tachycardia and PVCs on the ECG than those without asthma. The patients with asthma received β2-mimetics; the risk of tachycardia and PVCs is even more pronounced.
Pharmacoepidemiology and Drug Safety | 2015
Miriam J. Warnier; Frans H. Rutten; Patrick C. Souverein; Anthonius de Boer; Arno W. Hoes; Marie L. De Bruin
Monitoring of the QT duration by electrocardiography (ECG) prior to treatment is frequently recommended in the label of QT‐prolonging drugs. It is, however, unknown how often general practitioners in daily clinical practice are adhering to these risk‐minimization measures. We assessed the frequency of ECG measurements in patients where haloperidol was initiated in primary care.
PLOS ONE | 2014
Miriam J. Warnier; Frans H. Rutten; Anthonius de Boer; Arno W. Hoes; Marie L. De Bruin
Background Although it is known that patients with chronic obstructive pulmonary disease (COPD) generally do have an increased heart rate, the effects on both mortality and non-fatal pulmonary complications are unclear. We assessed whether heart rate is associated with all-cause mortality, and non-fatal pulmonary endpoints. Methods A prospective cohort study of 405 elderly patients with COPD was performed. All patients underwent extensive investigations, including electrocardiography. Follow-up data on mortality were obtained by linking the cohort to the Dutch National Cause of Death Register and information on complications (exacerbation of COPD or pneumonia) by scrutinizing patient files of general practitioners. Multivariable cox regression analysis was performed. Results During the follow-up 132 (33%) patients died. The overall mortality rate was 50/1000 py (42–59). The major causes of death were cardiovascular and respiratory. The relative risk of all-cause mortality increased with 21% for every 10 beats/minute increase in heart rate (adjusted HR: 1.21 [1.07–1.36], p = 0.002). The incidence of major non-fatal pulmonary events was 145/1000 py (120–168). The risk of a non-fatal pulmonary complication increased non-significantly with 7% for every 10 beats/minute increase in resting heart rate (adjusted HR: 1.07 [0.96–1.18], p = 0.208). Conclusions Increased resting heart rate is a strong and independent risk factor for all-cause mortality in elderly patients with COPD. An increased resting heart rate did not result in an increased risk of exacerbations or pneumonia. This may indicate that the increased mortality risk of COPD is related to non-pulmonary causes. Future randomized controlled trials are needed to investigate whether heart-rate lowering agents are worthwhile for COPD patients.
Huisarts En Wetenschap | 2014
Miriam J. Warnier
belangrijk pathofysiologisch mechanisme kunnen zijn. Een tweede ontstaansmechanisme is systemische inflammatie. In epidemiologische onderzoeken is bij COPD en astma een sterke relatie tussen systemische inflammatie en atherosclerose aangetoond.1 Daarnaast kan er bij astma en COPD door chronische hypoxie sprake zijn van autonome disfunctie. Dit leidt tot verhoogde sympathicusactiviteit, en onder andere tot een hogere rusthartslag.2 Verder kan medicatie voor COPD en astma een rol spelen bij het ontstaan van hartritmestoornissen. Beta-agonisten werken op de beta-2-adrenerge receptoren van de long. Deze receptoren zijn echter ook aanwezig in het hart, waardoor al sinds het beschikbaar komen van deze middelen in de jaren zestig rekening wordt gehouden met bijwerkingen op het hart. Deze middelen zijn onontbeerlijk bij de behandeling van obstructief longlijden, maar beta-agonisten en anticholinergica kunnen een tachycardie veroorzaken. Een verhoogde rusthartslag geeft een verhoogd risico op overlijden. Tot op heden zijn de resultaten van onderzoeken naar cardiovasculaire morbiditeit en mortaliteit bij gebruik van deze medicatie tegenstrijdig.3 Ook het gebruik van QT-verlengende medicatie, zoals macrolide antibiotica (erythromycine en azitromycine) of antipsychotica (haloperidol), speelt mogelijk een rol bij het ontstaan van ritmestoornissen bij patienten met obstructief longlijden.
The international journal of risk and safety in medicine | 2014
Miriam J. Warnier; Frank A. Holtkamp; Frans H. Rutten; Arno W. Hoes; Anthonius de Boer; Peter G. M. Mol; Marie L. De Bruin