Mostrando las entradas con la etiqueta asthma. Mostrar todas las entradas
Mostrando las entradas con la etiqueta asthma. Mostrar todas las entradas

23 mayo, 2013

Therapy with Omalizumab in Ireland

Omalizumab
Omalizumab (Photo credit: Wikipedia)

  Via: Dr. Ivancevich.

A study into efficacy of omalizumab therapy in patients with severe persistent allergic asthma at a tertiary referral centre for asthma in Ireland

  1. S.J. Lane
+ Author Affiliations
  1. From the Department of Respiratory Medicine, The Adelaide and Meath Hospital, Belgard Road, Tallaght, Dublin 24, Ireland
  1. Address correspondence to Dr A. Subramaniam, Department of Respiratory Medicine, The Adelaide and Meath Hospital, Belgard Road, Tallaght, Dublin 24, Ireland. email: dr.abisubra@gmail.com
  • Received December 31, 2012.
  • Revision received January 19, 2013.

Abstract

Background: Asthma is a chronic airway disease characterized by airway inflammation, bronchial hyperresponsiveness and airflow obstruction. Patients with persistent symptoms despite maximum standard treatment as per Global Initiative of Asthma guidelines are considered to have severe persistent asthma. Omalizumab is a recombinant humanized monoclonal antibody licenced for use as an add-on therapy in these patients. Aim: To assess the clinical benefit amongst responders to omalizumab therapy at a tertiary referral centre. Methods: This was a retrospective audit assessing the effect of omalizumab therapy on asthma control, frequency of exacerbation and hospitalization rates over 6 months before and after therapy. Results: The study included 30 responders (14 females). There was a reduction in exacerbation and hospitalization rates following initiation of omalizumab, 73 and 91%, respectively (P-value < 0.0001). The number of exacerbations decreased from 3.48 ± 2.20 to 0.93 ± 0.83 and the mean number of admissions decreased from 1.07 ± 1.1 to 0.1 ± 0.40 over the study duration (P < 0.001). There was 73% reduction in the weekly need for rescue salbutamol therapy with mean of 30.33 ± 6.49 puffs to 8.23 ± 1.51 puffs after omalizumab therapy (P < 0.0001). Seventy-nine per cent of patients were able to reduce their maintenance oral corticosteroid therapy. Conclusions: Overall, responders to omalizumab therapy are less likely to experience an asthma exacerbation and hospitalization. They were also more likely to reduce maintenance corticosteroid therapy and the need for rescue reliever therapy. These data suggest that omalizumab has proven effective in improving health outcomes for a cohort of carefully selected patients with severe allergic asthma in Ireland.
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29 abril, 2013

¿Montelukast fuera de indicación en preescolares?

Montelukast
Montelukast (Photo credit: mañsk)
 Source: Hemos leido
Gracias a la cuenta de Twitter de Evidencias en Pediatría (@evidpediatria), recordábamos nuestro post sobre el montelukast y su uso el bronquiolitis, que vimos pinchado en más de un corcho de nuestros centros de salud. Y uno se pregunta… ¿se usa montelukast fuera de indicación?
 
En nuestro ámbito sanitario no hemos encontrado datos publicados al respecto, pero hemos leído los resultados de un ensayo clínico publicado recientemente en Pediatrics, en donde se evaluó si el tratamiento profiláctico con montelukast  4 mg/día vs placebo durante 12 semanas, reducía laincidencia y la severidad de infecciones del tracto respiratorio superior, en niños sanos de edad preescolar (de entre 1 y 5 años de edad).
 
Este ensayo, realizado en Israel sobre 300 niños reclutados en 3 consultas pediátricas de atención ambulatoria, no mostró que redujera la incidencia de infecciones respiratorias del tracto superior, así como tampoco encontró diferencias en ninguna de las variables secundarias entre los dos grupos.
 
Revisando este tema nos preguntamos… ¿cómo habrá quedado el plan de gestión riesgos sobre el montelukast en pediatría, que se anunciaba en la sección 3 (Información sobre seguridad) del informe mensual de la AGEMED de febrero 2011 bajo el título Montelukast: notificación de casos de reacciones psiquiátricas?
 
El resumen de esa información decía: “se han notificado casos de alteraciones psiquiátricas y del comportamiento en pacientes tratados con montelukast. La revisión de los datos disponibles ha concluido que esta información está adecuadamente descrita en las fichas técnicas de los medicamentos que contienen montelukast. Adicionalmente se ha iniciado un plan de gestión de riesgos sobre el uso de montelukast en pediatría.”

07 abril, 2012

¿Qué evidencia existe para el tratamiento de sibilancias inducidas por infecciones virales en pacientes pediátricos con montelukast?

¿Qué evidencia existe para el tratamiento de sibilancias inducidas por infecciones virales en pacientes pediátricos con montelukast?

Barroso Espadero D. ¿Qué evidencia existe para el tratamiento de sibilancias inducida por infecciones virales en pacientes pediátricos con montelukast? Evid Pediatr. 2012;8:46.
Traducción autorizada de: TRIPanswers. What is the evidence for the treatment of viral induced wheeze in paediatric patients with Singulair? TRIP Database Limited. Servicio y Repositorio de Preguntas y Respuestas Clínicas: “TRIPanswers” (sitio web de TRIPanswers). Documento número 6851 [en línea] [fecha de actualización: 2012; fecha de consulta: 25-3-2012]. Disponible en: http://www.tripanswers.org/answer.aspx?qid=6851.
Artículo completo | PDF

Conclusion personal: parece que nos encontramos ante otro medicamento no mejor que un placebo. 
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27 marzo, 2012

In allergic children with asthma or rhinitis, is immunotherapy useful?

Source: Evidencias en Pediatria.
Full Text: PDF

Conclusiones de los autores del estudio: en niños y adolescentes con
 rinoconjuntivitis alérgica, la inmunoterapia no ha mostrado beneficio para
 disminuir los síntomas o la utilización de medicación. En el asma alérgica
 la inmunoterapia subcutánea parece reducir los síntomas y el uso de
 medicación, pero la evidencia es limitada en cuanto a la magnitud del efecto
. Además, no está exenta de efectos secundarios. La inmunoterapia
 sublingual en dosis altas produce mejoría sintomática y disminuye el uso de medicación en
 niños con asma y alergia a polen de gramíneas.
Comentario de los revisores: la prevalencia de las enfermedades alérgicas está aumentando
, generando importante morbilidad. El tratamiento con inmunoterapia no ha demostrado su 
eficacia, ya que produce mejorías estadísticamente significativas pero clínicamente poco
 importantes y con riesgo de efectos secundarios. Por ello no debe generalizarse su uso,
 reservándolo solo para casos concretos evaluados detenidamente.
Authors' conclusions: there is at present insufficient evidence that immunotherapy in any
 administration form has a positive effect on symptoms or  medication use in children and 
adolescents with allergic rhino conjunctivitis. In allergic asthma, the subcutaneous immunotherapy
 appears to reduce symptoms and use of medication but the evidence is limited concerning the
 size of benefit. It is not free of side effects. High doses sublingual inmmunotherapy produce
symptomatic improvement and medication use in children with asthma and allergies to grass pollen.
Reviewers' commentary: the prevalence of allergic diseases is increasing, and its burden is
 substantial. The efficacy of the treatment with allergen-specific immunotherapy has not been
 demonstrated; although the improvement has statistically significance, the clinical relevance is
 poor, with an increased risk of adverse reactions. Due to that, the use of immunotherapy should
 no be generalised, reserving it for cases thoroughly evaluated.


09 septiembre, 2011

Management of asthma in pregnancy guided by measurement of fraction of exhaled nitric oxide: a double-blind, randomised controlled trial



Management of asthma in pregnancy guided by measurement of fraction of exhaled nitric oxide: a double-blind, randomised controlled trial
Ms Heather Powell MMedSc,Vanessa E Murphy PhD,Prof D Robin Taylor MD,Prof Michael J Hensley PhD,Kirsten McCaffery PhD,Warwick Giles PhD,Vicki L Clifton PhD,Prof Peter G Gibson MBBS
The Lancet - 10 September 2011 ( Vol. 378, Issue 9795, Pages 983-990 )
DOI: 10.1016/S0140-6736(11)60971-9

Background


ber 201

Asthma exacerbations during pregnancy are common and can be associated with substantial maternal and fetal morbidity. Treatment decisions based on sputum eosinophil counts reduce exacerbations in non-pregnant women with asthma, but results with the fraction of exhaled nitric oxide (FENO) to guide management are equivocal. We tested the hypothesis that a management algorithm for asthma in pregnancy based on FENO and symptoms would reduce asthma exacerbations.

Methods

We undertook a double-blind, parallel-group, controlled trial in two antenatal clinics in Australia. 220 pregnant, non-smoking women with asthma were randomly assigned, by a computer-generated random number list, before 22 weeks’ gestation to treatment adjustment at monthly visits by an algorithm using clinical symptoms (control group) or FENO concentrations (active intervention group) used to uptitrate (FENO >29 ppb) or downtitrate (FENO <16 ppb) inhaled corticosteroid dose. Participants, caregivers, and outcome assessors were masked to group assignment. Longacting β2 agonist and minimum dose inhaled corticosteroid were used to treat symptoms when FENO was not increased. The primary outcome was total asthma exacerbations (moderate and severe). Analysis was by intention to treat. This study is registered with the Australian and New Zealand Clinical Trials Registry, number 12607000561482.

Findings

111 women were randomly assigned to the FENO group (100 completed) and 109 to the control group (103 completed). The exacerbation rate was lower in the FENO group than in the control group (0·288 vs 0·615 exacerbations per pregnancy; incidence rate ratio 0·496, 95% CI 0·325—0·755; p=0·001). The number needed to treat was 6. In the FENO group, quality of life was improved (score on short form 12 mental summary was 56·9 [95% CI 50·2—59·3] in FENO group vs 54·2 [46·1—57·6] in control group; p=0·037) and neonatal hospitalisations were reduced (eight [8%] vs 18 [17%]; p=0·046).

Interpretation

Asthma exacerbations during pregnancy can be significantly reduced with a validated FENO-based treatment algorithm.

Funding

National Health and Medical Research Council of Australia.

01 agosto, 2011

Asthma, placebo, and how not to kill your patients


Salbutamal metered dose inhaler.
Salbutamal metered dose inhaler. (Photo credit: Wikipedia)

A number of years ago I was walking along Lake Michigan with a friend (a fellow medical resident) when she turned to me and said, “are you wheezing?  Do you have asthma?”  I had always been physically active and assumed my breathlessness while walking down the trail was due to the thirty extra pounds of pizza and doughnuts I’d acquired during residency.  But she was right: I was wheezing and breathless and it didn’t feel good at all.  I made an appointment with one of the hospital’s lung docs who took a good history, did a physical, and ran some pulmonary function tests.  And I did have asthma.  And it felt much, much better when I            t got better when I lost 40 lbs and started treatment for my acid reflux.)
I still get mild asthma symptoms from time to time, especially when I get sick, but for many others, the picture isn’t so pretty.  Asthma kills at least a quarter of a million people every year around the world.   If you’ve ever worked in an ER and seen a kid with a bad asthma attack, you’ve earned a healthy respect for the disease.  If you’ve ever watched your own kid gasping for breath, begging you to make it better, you’ve learned to fear it.
As our understanding of asthma has improved, so has our ability to treat it (an ability that is strongly linked to a patient’s socio-economic status.  Mortality has been rising despite the discovery of better treatments.  Wait: let’s pull this out of the parentheses…)…  Asthma deaths and hospitalizations are largely preventable, and disproportionately affect Black and Hispanic Americans. We know how to treat thedisease asthma, but don’t know how to treat the people who are affected most.
We understand that asthma is not just a tightening of the airways but also an inflammation that can cause long-term damage.   Not only can we treat asthma, but we have objective ways of measuring how well our patients are doing.   It’s easy and inexpensive to measure airway obstruction and response to medications.  We know what works.
For this reason, a new study in the New England Journal of Medicineseems both wise and foolish. To see full article in PDF here. 
(I thought I was so on the ball.  I really did. But while I was busy riding my bike, playing with my kid, and looking at rentals with my wife, David Gorski and my other medical blogger pals were out in Las Vegas at TAM discussing the very study I wanted to tell you about.)
The study, called “Active albuterol or placebo, sham acupuncture, or no intervention in asthma,” was done for reasons that are not clear to me. It may have been done not to test the effectiveness of asthma therapy but to look at what a “placebo” might really be or do.  At least, I think that was the idea.  When reading the abstract and full text, it’s not actually clear why the study was done.  At first it seems as if it were done to see why asthmatics treated with placebo improve:
In prospective experimental studies in patients with asthma, it is difficult to determine whether responses to placebo differ from the natural course of physiological changes that occur without any intervention.
Why ask such a question? We know that poorly-treated asthma is deadly, and well treated asthma much less so.  Why do we care about placebo effects here?  The authors explain further:
Placebo effects (i.e., benefits resulting from simulated treatment or the experience of receiving care) are reported to improve signs and symptoms of many diseases in clinical trials and in clinical practice. On this basis, the accepted standards for clinical-trial design specify that the effects of active treatment should ideally be compared with the effects of placebo. Despite this common practice, it is unclear whether placebo effects observed in clinical trials (or those that presumably occur in clinical care) influence both objective and subjective outcomes and whether placebo effects differ from the natural course of disease or regression to the mean.
In other words, the authors want to know what placebos actually do to real people, and they chose asthmatics because they are easy to study (there are symptom-assessment tools for subjective data and spirometry for objective data).   This makes asthma both the right and wrong choice for the study.  It’s an excellent model to assess the affect of placebo, but one in which the use of placebo is hard to justify on an ethical basis.
Not surprisingly, they found that “doing something” worked better than doing nothing.  More specifically, they found that any placebo will make a patient feel subjectively better than doing nothing at all.   They also found that all three placebos (sham acupuncture, fake inhaled medicine, and simply being enrolled in the study without treatment) improve do bjective measures of lung function, but not nearly as much as real medicine (in fact, not much at all).
In other words, simply attending to a patient makes them feel better.  But to get a significant objective improvement (in asthma at least) you must also give them real medicine.  Real medicine comprises both active medications and attending to the patient.  There is no separate “placebo” that can be given to treat asthma effectively.
This is actually a quite beautiful study.  It demonstrates that “placebo effect” is not the same as a real treatment, that real treatment always includes whatever benefit placebo provides, and that placebo is mostly an effect on subjective rather than objective measures of health.  You can’t fix asthma with placebo, only with real treatment.  But we’ve already known that from decades of studying asthma.  So what other justification is there for doing this study?
Our research has important implications both for the treatment of asthma and for clinical-trial design in general. Many patients with asthma have symptoms that remain uncontrolled, and the discrepancy between objective pulmonary function and patients’ self-reports noted in this study suggests that subjective improvement in asthma should be interpreted with caution and that objective outcomes should be more heavily relied on for optimal asthma care. Indeed, although improvement in objective measures of lung function would be expected to correlate with subjective measures, our study suggests that in clinical trials, reliance solely on subjective outcomes may be inherently unreliable, since they may be significantly influenced by placebo effects. However, even though objective physiological measures (e.g., FEV1) are important, other outcomes such as emergency room visits and quality-of-life metrics may be more clinically relevant to patients and physicians. Although placebos remain an essential component of clinical trials to validate objective findings, assessment of the course of the disease without treatment, if medically appropriate, is essential in the evaluation of patient-reported outcomes. (Emphasis mine, PalMD)
Source: Science based-medicine
This is folly.  First, we have a huge literature on quality of life metrics in asthma.  Huge.  And we also know that objective changes in asthma are what save patients’ lives.  Yes, I care how my patient feels, but it is not more “clinically relevant” than how they are actually doing physiologically.  Both are important, but not equal.  And the idea that comparing active treatment to placebo is not ideal is not new to researchers.  It’s simply that following the natural history of the disease as a “control” is not usually appropriate (cf. Tuskegee syphilis experiment).
No good clinician would consider treating an asthmatic with placebo.  Improper treatment of asthma leads to debility and death.  This study chose mild asthmatics, but I still feel very uncomfortable with the ethics of the study design.  Rather than using a disease we know how to treat to study placebo, we should be finding ways to get treatment to the millions of people who aren’t getting it.
References
Wechsler ME, Kelley JM, Boyd IO, Dutile S, Marigowda G, Kirsch I, Israel E, & Kaptchuk TJ (2011). Active albuterol or placebo, sham acupuncture, or no intervention in asthma. The New England journal of medicine, 365(2), 119-26 PMID: 21751905



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