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

24 junio, 2013

Proton pump inhibitors and risk of fractures: a meta-analysis of 11 international studies

Line drawing of fractured hipImage via Wikipedia
Yu EW, Bauer SR, Bain PA, et al. Proton pump inhibitors and risk of fractures: a meta-analysis of 11 international studies.Am J Med. 2011 Jun;124(6):519-26. (Review) PMID: 21605729


BACKGROUND: Concerns have been raised about the risk of fractures with acid-suppressive medications, such as proton pump inhibitors and histamine(2)-receptor antagonists.
METHODS: This meta-analysis evaluated the association between proton pump inhibitor or histamine(2)-receptor antagonist use and fractures. We performed a systematic search of published literature (1970 to October 10, 2010) in MEDLINE, EMBASE, and other sources. Ten publications reporting 11 studies were considered eligible for analysis.
RESULTS: All studies were observational case-control or cohort studies and primarily evaluated older adults. The summary effect estimate for risk of hip fracture increased modestly among individuals taking proton pump inhibitors (relative risk [RR] 1.30, 95% confidence interval [CI], 1.19-1.43). There also was an increase in spine (RR 1.56, 95% CI, 1.31-1.85) and any-site fractures (RR 1.16, 95% CI, 1.04-1.30) among proton pump inhibitor users. These findings were similar in both men and women and after stratification by duration of use. In contrast, histamine(2)-receptor antagonist use was not significantly associated with increased risk of hip fracture (RR 1.12, 95% CI, 0.97-1.30).
CONCLUSION: In this meta-analysis of observational studies, proton pump inhibitors modestly increased the risk of hip, spine, and any-site fractures, whereas histamine(2)-receptor antagonists were not associated with fracture risk. The possibility of residual confounding cannot be excluded. Further skeletal evaluation should be considered for patients who are taking proton pump inhibitors and also at risk for osteoporotic fracture.

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16 junio, 2013

Probiotics for treating persistent diarrhoea in children

Percentage of rotavirus tests with positive re...Source: Pediatria Basada en la evidencia.

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10 junio, 2013

Vaccines to prevent influenza in healthy adults

Jefferson T, Di Pietrantonj C, Rivetti A, Bawazeer GA, Al-Ansary LA, Ferroni E
Published Online: 
June 4, 2013
Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). Without laboratory tests, doctors cannot tell the two illnesses apart. Both last for days and rarely lead to death or serious illness. At best, vaccines might be effective against only influenza A and B, which represent about 10% of all circulating viruses. Each year, the World Health Organization recommends which viral strains should be included in vaccinations for the forthcoming season.
Authors of this review assessed all trials that compared vaccinated people with unvaccinated people. The combined results of these trials showed that under ideal conditions (vaccine completely matching circulating viral configuration) 33 healthy adults need to be vaccinated to avoid one set of influenza symptoms. In average conditions (partially matching vaccine) 100 people need to be vaccinated to avoid one set of influenza symptoms. Vaccine use did not affect the number of people hospitalised or working days lost but caused one case of Guillian-Barré syndrome (a major neurological condition leading to paralysis) for every one million vaccinations. Fifteen of the 36 trials were funded by vaccine companies and four had no funding declaration. Our results may be an optimistic estimate because company-sponsored influenza vaccines trials tend to produce results favorable to their products and some of the evidence comes from trials carried out in ideal viral circulation and matching conditions and because the harms evidence base is limited..


Background: 
Different types of influenza vaccines are currently produced worldwide. Healthy adults are presently targeted mainly in North America.
Objectives: 
Identify, retrieve and assess all studies evaluating the effects of vaccines against influenza in healthy adults.
Search strategy: 
We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library, 2010, issue 2), MEDLINE (January 1966 to June 2010) and EMBASE (1990 to June 2010).
Selection criteria: 
Randomised controlled trials (RCTs) or quasi-RCTs comparing influenza vaccines with placebo or no intervention in naturally-occurring influenza in healthy individuals aged 16 to 65 years. We also included comparative studies assessing serious and rare harms.
Data collection and analysis: 
Two review authors independently assessed trial quality and extracted data.
Main results: 
We included 50 reports. Forty (59 sub-studies) were clinical trials of over 70,000 people. Eight were comparative non-RCTs and assessed serious harms. Two were reports of harms which could not be introduced in the data analysis. In the relatively uncommon circumstance of vaccine matching the viral circulating strain and high circulation, 4% of unvaccinated people versus 1% of vaccinated people developed influenza symptoms (risk difference (RD) 3%, 95% confidence interval (CI) 2% to 5%). The corresponding figures for poor vaccine matching were 2% and 1% (RD 1, 95% CI 0% to 3%). These differences were not likely to be due to chance. Vaccination had a modest effect on time off work and had no effect on hospital admissions or complication rates. Inactivated vaccines caused local harms and an estimated 1.6 additional cases of Guillain-Barré Syndrome per million vaccinations. The harms evidence base is limited.
Authors' conclusions: 
Influenza vaccines have a modest effect in reducing influenza symptoms and working days lost. There is no evidence that they affect complications, such as pneumonia, or transmission.
WARNING:
This review includes 15 out of 36 trials funded by industry (four had no funding declaration). An earlier systematic review of 274 influenza vaccine studies published up to 2007 found industry funded studies were published in more prestigious journals and cited more than other studies independently from methodological quality and size. Studies funded from public sources were significantly less likely to report conclusions favorable to the vaccines. The review showed that reliable evidence on influenza vaccines is thin but there is evidence of widespread manipulation of conclusions and spurious notoriety of the studies. The content and conclusions of this review should be interpreted in light of this finding.
This record should be cited as: 
Jefferson T, Di Pietrantonj C, Rivetti A, Bawazeer GA, Al-Ansary LA, Ferroni E. Vaccines for preventing influenza in healthy adults. Cochrane Database of Systematic Reviews 2013, Issue 6. Art. No.: CD001269. DOI: 10.1002/14651858.CD001269.pub4
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29 mayo, 2013

The Psychoterapy is alive

Comparative Efficacy of Seven Psychotherapeutic Interventions for Patients with Depression: A Network Meta-Analysis

 Source: PLOS MEDICINE

Authors:

  • Jürgen Barth 


  • Thomas Munder 

  • Heike Gerger,
  • Eveline Nüesch,
  • Sven Trelle,
  • Hansjörg Znoj,
  • Peter Jüni,
  • Pim Cuijpers

Abstract

Background

Previous meta-analyses comparing the efficacy of psychotherapeutic interventions for depression were clouded by a limited number of within-study treatment comparisons. This study used network meta-analysis, a novel methodological approach that integrates direct and indirect evidence from randomised controlled studies, to re-examine the comparative efficacy of seven psychotherapeutic interventions for adult depression.

Methods and Findings

We conducted systematic literature searches in PubMed, PsycINFO, and Embase up to November 2012, and identified additional studies through earlier meta-analyses and the references of included studies. We identified 198 studies, including 15,118 adult patients with depression, and coded moderator variables. Each of the seven psychotherapeutic interventions was superior to a waitlist control condition with moderate to large effects (range d = −0.62 to d = −0.92). Relative effects of different psychotherapeutic interventions on depressive symptoms were absent to small (range d = 0.01 to d = −0.30). Interpersonal therapy was significantly more effective than supportive therapy (d = −0.30, 95% credibility interval [CrI] [−0.54 to −0.05]). Moderator analysis showed that patient characteristics had no influence on treatment effects, but identified aspects of study quality and sample size as effect modifiers. Smaller effects were found in studies of at least moderate (Δd = 0.29 [−0.01 to 0.58]; p = 0.063) and large size (Δd = 0.33 [0.08 to 0.61]; p = 0.012) and those that had adequate outcome assessment (Δd = 0.38 [−0.06 to 0.87]; p = 0.100). Stepwise restriction of analyses by sample size showed robust effects for cognitive-behavioural therapy, interpersonal therapy, and problem-solving therapy (all d>0.46) compared to waitlist. Empirical evidence from large studies was unavailable or limited for other psychotherapeutic interventions.

Conclusions

Overall our results are consistent with the notion that different psychotherapeutic interventions for depression have comparable benefits. However, the robustness of the evidence varies considerably between different psychotherapeutic treatments.
Please see later in the article for the Editors' Summary

Editors' Summary

Background

Depression is a very common condition. One in six people will experience depression at some time during their life. People who are depressed have recurrent feelings of sadness and hopelessness and might feel that life is no longer worth living. The condition can last for months and often includes physical symptoms such as headaches, sleeping problems, and weight gain or loss. Treatment of depression can include non-drug treatments (psychotherapy), antidepressant drugs, or a combination of the two. Especially for people with mild or intermediate depression, psychotherapy is often considered the preferred first option. Psychotherapy describes a range of different psychotherapies, and a number of established types of psychotherapies have all shown to work for at least some patients.

Why Was This Study Done?

While it is broadly accepted that psychotherapy can help people with depression, the question of which type of psychotherapy works best for most patients remains controversial. While many scientific studies have compared one psychotherapy with control conditions, there have been few studies that directly compared multiple treatments. Without such direct comparisons, it has been difficult to establish the respective merits of the different types of psychotherapy. Taking advantage of a recently developed method called “network meta-analysis,” the authors re-examine the evidence on seven different types of psychotherapy to see how well they have been shown to work and whether some work better than others.

What Did the Researchers Do and Find?

The researchers looked at seven different types of psychotherapy, which they defined as follows. “Interpersonal psychotherapy” is short and highly structured, using a manual to focus on interpersonal issues in depression. “Behavioral activation” raises the awareness of pleasant activities and seeks to increase positive interactions between the patient and his or her environment. “Cognitive behavioral therapy” focuses on a patient's current negative beliefs, evaluates how they affect current and future behavior, and attempts to restructure the beliefs and change the outlook. “Problem solving therapy” aims to define a patient's problems, propose multiple solutions for each problem, and then select, implement, and evaluate the best solution. “Psychodynamic therapy” focuses on past unresolved conflicts and relationships and the impact they have on a patient's current situation. In “social skills therapy,” patients are taught skills that help to build and maintain healthy relationships based on honesty and respect. “Supportive counseling” is a more general therapy that aims to get patients to talk about their experiences and emotions and to offer empathy without suggesting solutions or teaching new skills.
The researchers started with a systematic search of the medical literature for relevant studies. The search identified 198 articles that reported on such clinical trials. The trials included a total of 15,118 patients and compared one of the seven psychotherapies either with another one or with a common “control intervention”. In most cases, the control (no psychotherapy) was deferral of treatment by “wait-listing” patients or continuing “usual care.” With network meta-analysis they were able to summarize the results of all these trials in a meaningful way. They did this by integrating direct comparisons of several psychotherapies within the same trial (where those were available) with indirect comparisons across all trials (using no psychotherapy as a control intervention).
Based on the combined trial results, all seven psychotherapies tested were better than wait-listing or usual care, and the differences were moderate to large, meaning that the average person in the group that received therapy was better off than about half of the patients in the control group. When comparing the therapies with each other, the researchers saw small or no differences, meaning that none of them really stood out as much better or much worse than the others. They also found that the treatments worked equally well for different patient groups with depression (younger or older patients, or mothers who had depression after having given birth). Similarly, they saw no big differences when comparing individual with group therapy, or person-to-person with internet-based interactions between therapist and patient.
However, they did find that smaller and less rigorous studies generally found larger benefits of psychotherapies, and most of the studies included in the analysis were small. Only 36 of the studies had at least 50 patients who received the same treatment. When they restricted their analysis to those studies, the researchers still saw clear benefits of cognitive-behavioral therapy, interpersonal therapy, and problem-solving therapy, but not for the other four therapies.

What Do these Findings Mean?

Similar to earlier attempts to summarize and make sense of the many study results, this one finds benefits for all of the seven psychotherapies examined, and none of them stood as being much better than some or all others. The scientific support for being beneficial was stronger for some therapies, mostly because they had been tested more often and in larger studies.
Treatments with proven benefits still do not necessarily work for all patients, and which type of psychotherapy might work best for a particular patient likely depends on that individual. So overall this analysis suggests that patients with depression and their doctors should consider psychotherapies and explore which of the different types might be best suited for a particular patient.
The study also points to the need for further research. Whereas depression affects large numbers of people around the world, all of the trials identified were conducted in rich countries and Western societies. Trials in different settings are essential to inform treatment of patients worldwide. In addition, large high-quality studies should further explore the potential benefits of some of therapies for which less support currently exists. Where possible, future studies should compare psychotherapies with one another, because all of them have benefits, and it would not be ethical to withhold such beneficial treatment from patients.

Additional Information

Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.1​001454.

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26 mayo, 2013

Tratamiento farmacologico de la migraña en niños y adolescentes

Fuente: Evidencias en Pediatria

PDF        English

AVC | Artículos Valorados Críticamente
El-Chammas K, Keyes J, Thompson N, Vijayakumar J, Becher D, Jackson JL. Pharmacologic Treatment of Pediatric Headaches: A Meta-analysis. JAMA Pediatr. 2013 Mar 1;167:250-8. D.O.I.: 10.1001/jamapediatrics.2013.508.

Revisores: Cuello García CA1, Pérez Gaxiola G2

1ITESM. Monterrey. Nuevo León (México).
2Hospital Pediátrico de Sinaloa. Culiacán. Sinaloa (México).
Correspondencia: Carlos Alberto Cuello García. Correo electrónico: carlos.cuello@gmail.com
Palabras clave: Migraña; Cefalea
Keywords: Migraine Disorders; Headache
Fecha de recepción: 19/04/2013   Fecha de aceptación: 02/05/2013   Fecha de publicación: 16/05/2013   

Resumen Estructurado


Objetivo: comparar la eficacia de diversos tratamientos farmacológicos en la prevención de cefalea en niños y adolescentes.
Diseño: revisión sistemática (RS) con metaanálisis (MA).
Fuente de datos: se realizaron búsquedas en PubMed, EMBASE y CENTRAL hasta agosto de 2012. Se buscó en referencias bibliográficas. No hubo restricción del idioma. No se contactó con otros autores. La búsqueda incluyó medicamentos alfa-bloqueantes, bloqueadores del receptor de la angiotensina, anticonvulsivos, beta-bloqueantes, bloqueadores de los canales del calcio, inhibidores de la recaptación de la serotonina, agonistas de la serotonina y antidepresivos tricíclicos.
Selección de estudios: se limitó la búsqueda a ensayos clínicos aleatorios que evaluaron la eficacia de los medicamentos, comparados con placebo o con otro medicamento, para reducir la frecuencia o gravedad de cefaleas en menores de 18 años. Se incluyeron estudios con pacientes con migraña, cefalea tensional y cefalea crónica diaria.
Extracción de datos: la eligibilidad, la calidad y los datos de los estudios fueron evaluados de manera independiente por al menos dos autores, y las discrepancias se resolvieron por consenso. La calidad de los estudios se evaluó mediante la herramienta de valoración de sesgos de Cochrane y la escala de Jadad. El desenlace primario a evaluar fue la diferencia en la media de frecuencia de la cefalea con su intervalo de confianza del 95% (IC 95%), definida como número de eventos al mes, a las 12 semanas de seguimiento. Se realizó metaanálisis usando el modelo de efectos aleatorios para medicamentos individuales y también para grupos de medicamentos que tienen un mecanismo de acción similar. Se evaluó el efecto placebo mediante metarregresión. La heterogeneidad se evaluó con la I2. Se buscó sesgo de publicación con los métodos de Peters y de Egger.
Resultados principales: se incluyeron 21 ensayos clínicos (13 comparando con placebo, y 10 comparando entre medicamentos). Veinte de los ensayos incluyeron pacientes con migraña. Solo dos medicamentos alcanzaron significancia estadística: el topiramato (tres ensayos) redujo el número de episodios mensuales en -0,71 (IC 95%: -1,19 a -0,24), y la trazodona (un ensayo) los redujo por -0,60 ( IC 95%: -1,09 a -0,11). No se encontró sesgo de publicación. Los medicamentos con mayor número de efectos secundarios fueron el topiramato y el valproato.
Conclusión: el topiramato y la trazodona podrían disminuir los episodios mensuales de cefalea en pacientes menores de 18 años.
Conflicto de intereses: no existe.
Fuente de financiación: no se menciona.

Comentario Crítico


Justificación: la cefalea tensional y la migraña son entidades clínicas de frecuente presentación en niños y adolescentes. La prevalencia fluctúa alrededor del 15% para la cefalea tensional y del 4% para la migraña1, para la cual existen variados tratamientos farmacológicos, tanto para el tratamiento en la fase aguda (abortivos) como para prevenir la misma (profilácticos), cuya cantidad justifica una revisión sistemática de la evidencia. Dentro de los medicamentos profilácticos se encuentran los antiepilépticos, antidepresivos, antihistamínicos, bloqueadores del canal del calcio, antihipertensivos y antinflamatorios no esteroides (AINE). La presente revisión sistemática se enfoca a las terapias profilácticas.
Validez o rigor científico: se trata de una revisión sistemática con metaanálisis de ensayos clínicos aleatorios (ECA). Se incluyeron tanto los estudios que comparaban las terapias con placebo, como aquellos que comparaban terapias entre sí. La metodología de la presente revisión es adecuada, la población del estudio se define claramente, así como el factor de estudio (cefaleas en menores de 18 años), con una búsqueda exhaustiva, sensible y sin limitaciones. Tanto el cribado como la extracción de datos, la evaluación del sesgo de los estudios individuales, la evaluación de heterogeneidad, la búsqueda por sesgo de publicación y la estimación puntual mediante MA se pueden considerar adecuados. Es de notar que hubo 21 ECA que incluían a niños, adolescentes y adultos en el mismo estudio y que los autores no incluyeron en la revisión sistemática/metaanálisis porque no se podía separar por grupos de edad con los datos obtenidos. La heterogeneidad entre los estudios se detectó en el subgrupo de flunarizina (I2 = 85%), y propranolol (I2 = 84%) frente a placebo.
Importancia clínica: los únicos dos medicamentos que, al compararse con placebo, presentaron diferencias significativas matemáticas fueron el topiramato, con 0,7 episodios menos al mes  (IC 95%: 1,19 a 0,24) y la trazodona, con 0,6 episodios menos al mes (IC 95%: 1,09 a 0,11). Esta diferencia, sin embargo, es mínima, pues en los pacientes en estudio, el promedio de episodios de cefalea iba desde 3,8 hasta 13,5 al mes (media de 7,1), es decir, estas terapias disminuirán en promedio, de siete episodios/mes, a solo seis al mes. Por otra parte, si tenemos en cuenta el desenlace dicotómico de mejoría (o no mejoría) en al menos un 50% en el número de episodios, solo un estudio, con serias deficiencias metodológicas, que comparó propranolol frente a placebo pudo demostrar este efecto benéfico. Ni el topiramato ni la trazodona pudieron demostrar este resultado. Es de notar que el placebo tuvo un efecto significativo de reducir los episodios de 5,6/mes a 2,9/mes (p = 0,03); mejor que muchos medicamentos aquí estudiados. En una revisión sistemática de la Cochrane del año 20032,se encontró alguna evidencia a favor de flunarizina pero con baja calidad metodológica. Igualmente, en otra RS3 no incluida en este metaanálisis que comentamos, se encontró cierto efecto protector del topiramato, pero con efectos secundarios importantes, ambas revisiones fueron comentadas en una articulo anterior de nuestra revista4.
Aplicabilidad en la práctica clínica: la evidencia hallada en esta revisión sistemática presenta una calidad moderada a baja, principalmente por riesgo de sesgo, y moderada heterogeneidad para el desenlace de reducción de los episodios de cefalea. La recomendación clínica que se puede obtener sólo puede considerarse débil para prescribir topiramato o trazodona, siempre y cuando se tenga en mente y se comunique a los pacientes y padres que el efecto es mínimo y puede no ser satisfactorio, tanto para el clínico como para el paciente.
Conflicto de intereses de los autores del comentario: no existe.

Cómo citar este artículo

Cuello García CA, Pérez Gaxiola G. La evidencia para el tratamiento de la cefalea y la migraña en niños y adolescentes sigue siendo limitada. Evid Pediatr. 2013;9:26.

Bibliografía


  1. Arruda MA, Guidetti V, Galli F, Albuquerque RC, Bigal ME. Primary headaches in childhood: a population-based study. Cephalalgia. 2010;30:1056-64.
  2. Victor S, Ryan SW. Drugs for preventing migraine headaches in children. Cochrane Database Syst Rev. 2003;4:CD002761.
  3. Bakola E, Tzoufi M, Damigos D, Mavreas V. Anticonvulsant drugs for pediatric migraine prevention: An evidence-based review. Eur J Pain. 2009;13:893-901.
  4. García Lara NR, Frías García ME. Tratamiento preventivo para la migraña en niños: cuándo y cómo. Evid Pediatr. 2010;6:3.
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