Mostrando las entradas con la etiqueta Cochrane Collaboration. Mostrar todas las entradas
Mostrando las entradas con la etiqueta Cochrane Collaboration. Mostrar todas las entradas

04 julio, 2013

CCC The steps of a Cochrane Review, an overview

Published on Jul 3, 2013


What makes Cochrane Reviews different from other systematic reviews? Who -and what- is involved in the process? John K. MacDonald will introduce you to the steps of a Cochrane Review and give you some practical tips for getting a review underway.

Recording of the webinar held live on 13 June 2013.

16 junio, 2013

Probiotics for treating persistent diarrhoea in children

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

Image via Wikipedia
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12 junio, 2013

Más criticas al cribado de cáncer de mama

Shown is a breast being compressed to get the ...Visión crítica sobre la detección de cáncer de mama mediante mamografía (Revisión Cochrane)

Cochrane Collaboration
Cochrane Collaboration (Photo credit: Wikipedia)
Peter C. Gøtzsche es un conocido investigador danés líder del Centro Nórdico Cochrane de Copenhague, Dinamarca. Ha escrito numerosas evaluaciones dentro de la colaboración Cochrane.
Además de sus trabajos criticos sobre la investigación con placebos y los posibles sesgos de los metaanálisis es especialmente conocido por su voz crítica sobre el cribado del cancer de mama, sobre los que ya publicó un artículo de 2000 en Lancet (Is screening for breast cancer with mammography justifiable?).
Acaba de publicarse una revisión Cochrane sobre el screening de cancer de mama mediante mamografía escrita por él en colaboración con Karsten Juhl Jørgensen. Creo que se trata de una revisión que invita a la reflexión. Me he permitido traducir las conclusiones:
Shown is a breast being compressed to get the optimum mammographic image. (Photo credit: Wikipedia)
Implicaciones para la Práctica Clínica
Creemos que ha llegado el momento de reevaluar si la mamografía de cribado universal debería ser recomendada para cualquier grupo de edad. La disminución de las tasas de mortalidad por cáncer de mama se deben principalmente a la mejora de los tratamientos y la concienciación sobre el cáncer de mama, por lo que no estamos seguros de los beneficios del cribado en la actualidad. El sobrediagnóstico tiene costes humanos y aumenta el número de mastectomías y muertes. La probabilidad de que una mujer se beneficie del asistir a las pruebas  de cribado es pequeña, y en el mejor de los casos – si nos basamos en los resultados de ensayos aleatorios – diez veces más pequeño que el riesgo de que pueda experimentar daños graves en términos de sobrediagnóstico. Las mujeres, los médicos y los responsables políticos deben valorar cuidadosamente ventajas y desventajas cuando se decide si es adecuado o no asistir o apoyar programas de cribado.
Los defensores del cribado y de diversas  organizaciones en general han hecho hincapié en los beneficios y omitido información sobre los principales daños en sus materiales de información (Dixon-Woods, 2001; Gøtzsche 2012; Jørgensen 2004; Folleto NHS 2001; Folleto NHS 2010; EE.UU. Task Force 2002) y en cartas de invitación (Jørgensen 2006; Gøtzsche 2009). Por tanto la mayoría de las mujeres tienden a exagerar considerablemente los beneficios y no ser conscientes de los principales efectos nocivos del cribaje (Barratt 1997; Barratt 1999; Domenighetti 2003, Schwartz 2000).
Para intentar ayudar a asegurar que la mujer reciba una información adecuada para decidir si acudir o no a un programa de cribado, hemos redactado un folleto para pacientes basado en la evidencia disponible (Gøtzsche 2009). El folleto ha sido probado cuidadosamente entre los médicos generales y pacientes. Está disponible en el sitio web de BMJ en Inglés (Gøtzsche 2009) y en varios idiomas en el sitio web del Centro Nórdico Cochrane en http://www.cochrane.dk (acceso al folleto en español)
Se ha sugerido que estos recursos podrían redirigirse a intervenciones con beneficios comprobados en el cáncer de mama (Baum 2000) o utilizarse para otros fines (NBCC 2002). En comparación, el beneficio es al menos 200 veces mayor en las mujeres con cáncer de mama con ganglios positivos que son tratados con tamoxifeno ya que la extensión media de vida es de seis meses a los 10 años (EBCTCG 1998).
Implicaciones para la investigación
La mortalidad por cáncer de mama resulta poco fiable como medida de resultado de las pruebas de cribado (y por tanto también de los estudios de cohortes sobre eficacia de los programas nacionales) y exagera su beneficio. Debido a los problemas metodológicos de los ensayos de detección y los análisis reaalizados, sería útil que investigadores independientes realizaran un metanálisis basado en datos de pacientes individuales, donde no se permitiera la exclusión de las mujeres al azar. También sería útil obtener datos sobre todas las muertes por cáncer  de todos los ensayos ya que la clasificación errónea de la causa de la muerte a menudo se refiere a muertes por otros cánceres. Por último, es necesario investigar en métodos que permitan diferenciar los cánceres susceptibles de producir mayor mortalidad de los muchos tumores benignos identificados que no necesitarían tratamiento.

07 mayo, 2013

¿Debemos vacunar frente a la gripe a todos los niños?

AVC | Artículos Valorados Críticamente
Jefferson T, Rivetti A, Di Pietrantonj C, Demicheli V, Ferroni E. Vaccines for preventing influenza in healthy children (review). Cochrane Database Syst Rev. 2012;8:CD004879. D.O.I.: 10.1002/14651858.CD004879.pub4. 

English Version

Full Text PDF 

Revisores: Molina Arias M1, González de Dios J2

1Servicio de Gastroenterología y Nutrición. Hospital Infantil Universitario La Paz. Madrid. (España).
2Departamento de Pediatría. Hospital General Universario de Alicante. (España).
Correspondencia: Manuel Molina Arias. Correo electrónico: mma1961@gmail.com
Palabras clave: vacuna antigripal; seguridad; revisiones sistemáticas; niño; lactante; eficacia
Keywords: influenza vaccines; security; systematic reviews; child, preschool; infant; effectiveness
Fecha de recepción: 12/11/2012   Fecha de aceptación: 04/11/2012   Fecha de publicación: 12/12/2012   

Resumen Estructurado

Objetivo: estudiar los efectos de las vacunas antigripales disponibles en niños sanos para valorar su eficacia, su efectividad y los datos disponibles sobre su seguridad.
Diseño: revisión sistemática con metaanálisis.
Fuentes de datos: se buscaron estudios publicados hasta noviembre de 2011 en CENTRAL (Cochrane Central Register of Controlled Trials), MEDLINE (desde 1966) y EMBASE (desde 1974), sin restricciones de lenguaje ni de tipo de publicación. Además, se revisó la web del Vaccine Adverse Event Reporting System y se contactó con los fabricantes y los autores de los estudios más relevantes buscando datos no publicados.
Selección de estudios: ensayos clínicos aleatorizados (ECA), cuasi aleatorizados y comparativos, estudios de cohortes (ECh) y estudios de casos y controles (ECC) que comparaban los efectos de las vacunas antigripales, en cualquiera de las pautas utilizadas, frente a placebo o a no intervención en niños sanos menores de 16 años. Se consideraron también los trabajos sobre las vacunas más nuevas y las pendientes de uso autorizado. Se excluyeron los que incluían enfermos crónicos o inmunodeficientes.
Extracción de los datos: dos autores excluyeron de forma independiente los trabajos que no cumplían los criterios de inclusión, recurriendo al arbitraje de un tercero en caso de desacuerdo. Cuatro revisores extrajeron los datos utilizando un formulario previamente diseñado. Se registraron los datos sobre la calidad metodológica de los estudios, su diseño, las características de los participantes, el tipo de vacuna, las variables de resultado, el estado de publicación y la localización y fecha del trabajo. Se valoró el riesgo de sesgo de cada trabajo. Se analizaron separadamente los datos de las vacunas de virus vivos (VVV) y las inactivadas (VVI), así como los de menores de dos años, de dos a seis años y mayores de seis años. El efecto de la vacunación se midió con riesgos relativos (RR) en las comparaciones de ECA y ECh y con odds ratio (OR) en el único ECC analizado. Se realizó un análisis de sensibilidad excluyendo los trabajos traducidos del ruso y los que tenían alto riesgo de sesgo.
Resultados principales: se inluyeron 75 trabajos, aunque solo 41 fueron aptos para el metaanálisis. Se obtuvieron datos sobre efectividad y eficacia de 17 ECA, 19 ECh y 11 ECC.
La eficacia de las VVV en los ECA fue del 80% entre los dos y los seis años (RR: 0,2; intervalo de confianza del 95% [IC 95%]: 0,13 a 0,32), con un número necesario de vacunaciones para prevenir un  caso de gripe (NNV) de seis entre 2 y 16 años. No fue posible extraer conclusiones en menores de dos años. La eficacia de las VVI fue del 59% (RR: 0,41; IC 95%: 0,29 a 0,59), con un NNV de 28 en mayores de seis años. No se observaron diferencias con el placebo en los menores de dos años. Los resultados de efectividad fueron menores: 33% para las VVV (RR: 0,67; IC 95%: 0,62 a 0,72) y 36% para las VVI (RR: 0,64; IC 95%: 0,54 a 0,76; NNV: 8). No pudieron extraerse conclusiones en menores de dos años. El efecto de la vacunación fue algo mayor en los estudios observacionales en mayores de dos años, no observándose diferencias con el placebo en menores de esta edad.
No hubo diferencias en las variables secundarias (número de casos secundarios, de infección respiratoria baja, de otitis o de aumento de prescripciones farmacéuticas). Existen algunas pruebas de que disminuye el absentismo escolar y el laboral de los cuidadores, pero basadas en datos escasos.
La falta de homogeneidad impidió el análisis cuantitativo adecuado de los datos de seguridad.
Conclusión: las políticas nacionales de vacunación antigripal a niños sanos se basan en datos poco fidedignos. Las vacunas son eficaces para prevenir la enfermedad en mayores de dos años, pero se dispone de pocas pruebas sobre la eficacia en los menores de esta edad. Se necesitan más ensayos aleatorizados para probar la eficacia y la seguridad de las vacunas antigripales, especialmente de las VVI y en el grupo de niños de menor edad.
Conflicto de intereses: uno de los autores fue consultor de F. Hoffman-La Roche Ltd. en 1998-1999, aunque no recibe honorarios por publicaciones sobre inhibidores de neuraminidasa.
Fuente de financiación: Regione Piemonte ASL AL, Italia. MRC Programme Grant G0000340, Reino Unido.

Comentario Crítico


Justificación: existen grandes diferencias en las recomendaciones sobre la vacunación antigripal entre Europa y EE. UU. En este último, el Advisory Committee on Immunization Practices (ACIP) recomienda la vacunación universal en mayores de seis meses (ACIP 2010)1. Sin embargo, las recomendaciones para vacunar a niños sanos en Europa son menos frecuentes. El Comité Asesor de Vacunas de la Asociación Española de Pediatría (CAV-AEP) recomienda vacunar a los mayores de seis meses pertenecientes a grupos de riesgo y a los niños mayores de esta edad y adultos sanos que convivan con niños de riesgo2. Esto se debe a los datos previos disponibles sobre la baja efectividad y eficiencia de la vacuna (sobre todo en los niños de menor edad), los escasos datos sobre su seguridad y su baja aceptabilidad (una inyección intramuscular anual)2. En este sentido, la revisión de la literatura científica disponible puede aportar datos sobre la eficacia, la efectividad y la seguridad de la vacunación antigripal en niños.
Validez o rigor científico: se define claramente la población de estudio, la intervención analizada y los resultados considerados para su análisis. La búsqueda se realizó en bases de datos amplias, sin restricción idiomática ni de tipo de estudio. Se detallan los descriptores de búsqueda y el diagrama de flujo de selección. Se buscaron también datos no publicados contactando con los fabricantes y los autores de los estudios relevantes. Los trabajos se incluyeron independientemente por dos autores, con el arbitraje de un tercero cuando fue necesario. Cuatro revisores realizaron una revisión metodológica de los trabajos y los clasificaron según su riesgo de sesgo. Se valoró la heterogeneidad de los datos, incluyendo en el metaanálisis solo los adecuados. Por último, se estratificaron los efectos por los grupos de edad habituales y se hizo un análisis de sensibilidad con los trabajos que podrían modificar las conclusiones globales.
Importancia clínica: esta revisión complementa la realizada previamente por los mismos autores3, obteniendo unos resultados similares y sin aclarar puntos de interés como la eficacia-efectividad en menores de dos años y la seguridad a medio y largo plazo. Una efectividad global de las VVI del 60% apoyaría la recomendación de la vacunación antigripal universal en la infancia. El problema es la falta de pruebas concluyentes de eficacia en menores de dos años, aunque este hecho puede deberse a la ausencia de estudios suficientes y a las limitaciones de los existentes: falta de emparejamiento adecuado entre cepas vacunales y circulantes en el momento del estudio y el hecho de haber recibido una dosis de vacuna en lugar de las dos recomendadas en este grupo4. En este sentido, Manzoli et al.5 realizaron una revisión sistemática de ECA, encontrando únicamente tres estudios con datos en menores de dos años, por lo que tampoco pudieron extraer conclusiones firmes. Aunque tampoco se observan datos concluyentes sobre el efecto de las variables secundarias, sí existen datos sobre el probable efecto sobre la disminución del absentismo escolar. Otros autores5 encuentran también disminución de infecciones en niños vacunados. Por último, las revisiones centradas en VVI6 (las disponibles en España) permiten recomendar la vacunación de sujetos sanos con un alto grado de evidencia, aunque, una vez más, los datos en menores de dos años son escasos.
Por último, los datos sobre seguridad aportados por la presente revisión son tan heterogéneos que no permiten su análisis combinado ni extraer conclusiones firmes, aunque sí se han comunicado efectos adversos graves con algún tipo de vacunas. En cualquier caso, no parecen existir datos preocupantes sobre efectos adversos graves relacionados con las vacunas administradas en nuestro medio6.
Aplicabilidad a la práctica clínica: la revisión global de la literatura (no limitada a la revisión sistemática aquí analizada) permite concretar que la vacunación antigripal universal es una medida recomendable en la infancia, con una buena relación beneficios-riesgos-costes. Sin embargo, dadas las dificultades de la implementación sistemática de la vacunación antigripal en España y la falta de pruebas concluyentes en un grupo tan relevante como son los menores de dos años, parece oportuno reiterar las recomendaciones actuales hasta disponer de nuevos estudios sobre eficacia y seguridad, y obtener vacunas más eficaces.
Conflicto de intereses de los autores del comentario: no existe.

Cómo citar este artículo

Molina Arias M, González de Dios J. ¿Debemos vacunar frente a la gripe a todos los niños? Evid Pediatr. 2013;9:6.

Bibliografía


  1. Fiore AE, Uyeki TM, Broder K, Finelli L, Euler GL, Singleton JA, et al. Prevention and control of  influenza with vaccines: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2010. MMWR Recomm Rep. 2010;59:1-62.
  2. Moreno Pérez D, Arístegui Fernández J, Ruiz Contreras J, Álvarez García FJ, Merino Moína M, González Hachero J, et al. Vacunación frente a la gripe estacional en la infancia y la adolescencia. Recomendaciones del CAV-AEP para la campaña 2011-2012. An Pediatr (Barc). 2012;76:44.e1-e5.
  3. Jefferson T, Rivetti A, Harnden A, Di Pietrantonj C, Demichelli V. Vaccines for preventing influenza in healthy children. Cochrane Database Syst Rev. 2012;8:CD004879.
  4. Negri E, Colombo C, Giordano L, Groth N, Apolone G, La Vecchia C. Influenza vaccine in healthy children: a meta-analysis. Vaccine. 2005;23:2851-61.
  5. Manzoli L, Schioppa F, Boccia A, Villari P. The efficacy of influenza vaccine for healthy children: a meta-analysis evaluating potential sources of variation in efficacy estimates including study quality. Pediatr Infect Dis J. 2007;26:97-106.
  6. Michiels B, Govaerts F, Remmen R, Vermeire E, Coenen S. A systematic review of the evidence on the effectiveness and risks of inactivated influenza vaccines in different target groups. Vaccine. 2011;29:9159-70.
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10 abril, 2013

News from Trip database


Latest evidence.

These can be edited via the ‘Edit my profile’ link below.

Lots has been going on in the last month and we released a new content area – controlled trials (mainly randomised controlled trials). We have added approximately 500,000 trials to Trip. Just search the site normally and select the ‘Controlled trials’ link on the right hand side of the results page. For further information read this link and this link.

I had the pleasure of presenting at Evidence Live 2013 and have written up the main points of my presentation, which is a critique of the Cochrane Collaboration, this can be read here. My basic point is that the current methods are unsustainable, which is a real worry. I think Cochrane should concentrate their efforts of reducing the cost (finance, time, opportunity) for each systematic review. Systematic reviews are vital and therefore we need as many as we can get!

One little feature of interest is our ‘Share feature’ (click here for further information). This allows users to easily share results on Trip via email and social media. It really is easy to use!

FULL TEXT ALERT! Finally, we’re working hard to push out a new batch of updates to Trip, possibly by the middle of May. One key area that we need some input in is the full-text link outs - to allow the seamless linking between Trip and an institutions full-text holdings. We know this is important as many people have been asking for this for years. So, we need librarians and clinicians to work with us to achieve this. If you’re interested in linking Trip up to your organisations full-text documents then please let me know.

Best wishes

Jon

Jon Brassey
Trip Database

09 abril, 2013

A critique of the Cochrane Collaboration

Cochrane Collaboration
Cochrane Collaboration (Photo credit: Wikipedia)

A critique of the Cochrane Collaboration

What follows is a summary of a longer paper on some of the problems that the Cochrane Collaboration face.  It is based on the presentation I gave at Evidence Live 2013 entitled ‘Anarchism, Punk and EBM’. 

But to begin with I want to make it clear that I am fully supportive of systematic reviews and the reasons for doing them.  I also want to make it clear that this is not a criticism of the many thousands of volunteers who give their time freely to improve global healthcare.  I am in awe of their efforts.  My criticism is based on the fact that I feel that the current methods are unsustainable. 

Relevancy to clinical practice.

I have run a number of clinical question answering and between them have answered over 10,000 clinical questions.  It is very rare for a single systematic review to answer a question.  In an analysis of 358 dermatology questions only three could be answered by a single systematic review, so less than 1%.  Although we have only formally analysed dermatology there is little sense that many other areas do noticeably better, but there are some e.g. respiratory (but that would still answer fewer than 5% of the respiratory questions. In answering clinical questions I wish we had more systematic reviews that were useful for my work.  Should systematic reviews answer real questions?

Methodology

On average a Cochrane systematic review takes 23 months from protocol to publication [1] and hundreds if not thousands of hours [2]. This causes problems with both production and subsequent updating of reviews.  Clearly, with a finite resource the longer a systematic review takes to produce the fewer you can do.

In 2009 only 39.8% of their systematic reviews were up to date (using Cochrane’s own definition of being updated within the past two years) while by 2012 it had dropped further to 35.8% [1]

These figures are slightly mis-leading as the number of systematic reviews has increased in that time.  In 2009 there were 3,958 active reviews and in 2012 that figure had risen to 4,905.  So, in 2009, of the 3,958 reviews, only 1,575 were up to date.  In 2012, of the 4,905 reviews, only 1,756 were up to date – an increase in up to date reviews of just 181 in three years.  Putting this another way, in 2009 there were 2,383 out of date systematic reviews and in 2012 this had risen to 3,149.
These figures are terrible and are made worse by the relatively recent increase in funding and spending Cochrane has enjoyed [3].


In the last seven years of financial figures the Cochrane Collaboration has spent in excess of £100 million and over the twenty years it has existed this is likely to be over £150 million – over a quarter of a billion US Dollars.  It is probably redundant to point out that this is a vast sum. [UPDATE: it has been pointed out that £150 million is actually not that much and could be seen as a pittance - I guess it depends on perspective].

As well as significant financial support Cochrane has the selfless support of 28,000 volunteers. Yet, the number of active systematic reviews is still modest.  This indicates that the current system is unsustainable and not fit for purpose.  The methodology, while reducing some bias, has resulted in a huge cost increase, not just financial but also opportunity cost. Ironically, the case of Tamiflu highlights that the methodology is flawed.


Tamiflu

I do not wish to repeat the Tamiflu story here, for those interested there are numerous opportunities to find out more [4, 5].  In the latter reference, Tom Jefferson states:

“…I personally believe and my colleagues believe with me that Cochrane Reviews based on publications should really be a thing of the past…”

This is based on the fact that, when preparing the first Cochrane systematic review on neuraminidase inhibitors for preventing and treating influenza in healthy adults and children Tom and his team only relied on published journal articles [6].  This was subsequently found to miss large amounts of data, most of which was made available for the regulatory agencies e.g. EMA, FDA.  The updated, 2012, review [7] was a huge undertaking, even by Cochrane standards, but it was the only way Tom and his team felt they could obtain accurate estimations of the effect of neuraminidase inhibitors. 

But Tom is not alone in concerns about methodology, concerns with relying on aggregated trial data were made by Jack Cuzick, at Evidence Live 2013.  He made a general call for reviews to be based on individual patient data (IPD).

Both Tom and Jack feel that the current Cochrane methodology is not capable of making an accurate assessment of an interventions ‘worth’, albeit for different reasons.  The seriousness of this challenge should not be underestimated, it attacks at the very heart of the Cochrane Collaboration. 

Is there any hope?

In recent years there have been a number of articles that have suggested, to differing degrees, that doing things more quickly can give you the same or similar results to the Cochrane methodology.  I will highlight three:

1)    Can we rely on the best trial? A comparison of individual trials and systematic reviews [8].  In this paper the authors (including me) explored a random sample of Cochrane systematic reviews to see how often the largest randomised trial was in agreement with the subsequent meta-analysis.  This occurred in 81% of the meta-analyses examined and if the largest RCT was positive and significant it was around 95%.  In other words, using the largest RCT can give a broad hint as to the likely result of a subsequent meta-analysis.

2)    McMaster Premium LiteratUre Service (PLUS) performed well for identifying new studies for updated Cochrane reviews [9]. In this study the authors compared the performance of McMaster Premium LiteratUre Service (PLUS) and Clinical Queries (CQs) to that of the Cochrane Controlled Trials Register, MEDLINE, and EMBASE for locating studies added during an update of reviews. They concluded that PLUS included less than a quarter of the new studies in Cochrane updates, but most reviews appeared unaffected by the omission of these studies.  In other words, you do not necessarily need to get all articles to arrive at an accurate effect size (compared to the Cochrane systematic review).

3)    A pragmatic strategy for the review of clinical evidence [10].  In this paper the authors compared a research strategy based on the review of a selected number of core journals, with that derived by an SR in estimating the efficacy of treatments.  The authors concluded “We verified in a sample of SRs that the conclusion of a research strategy based on a pre-defined set of general and specialist medical journals is able to replicate almost all the clinical recommendations of a formal SR.”. Essentially, the same message as 2) above. 

The future

It is a very easy concept, the greater the cost (finance, time etc) of a systematic review the fewer systematic reviews within a fixed budget can be undertaken and kept updated.  Therefore, a major focus for Cochrane should be on reducing the cost per review.  Cochrane is full of incredibly talented people who appear to focus predominantly on reducing bias and random error.  This, to me, is a clear example of the laws of diminishing returns.  I would set the major challenge, for the next five years of Cochrane, to be – how to do a systematic review in a month (or less).

This side-steps the issue of regulatory data and/or IPD!

I see a future for Cochrane as having two types of systematic review: rapid systematic reviews undertaken in a significantly reduced timeframe, and a more costly systematic review that includes regulatory data and/or IPD.  If Cochrane can reduce the cost of a systematic review to around 10% of what it is now it means they can do ten times as many.  Or Cochrane might choose to do fewer than ten times as many rapid systematic reviews and leave any remaining resource to do the more costly systematic reviews.  The issues becomes (i) when can Cochrane ‘get away’ with a low-cost systematic review and (ii) when a high-cost review warranted.  These are questions requiring a research base to answer the questions, as well as being a question of values.

The argument has been made to me that there is a negative cost of doing a low-cost systematic review that might generate the ‘wrong’ answer.  While I appreciate this could be a scenario I would reply that while you’re busy doing one systematic review ‘correctly’ you are neglecting 5-10 rapid systematic reviews that might generate significantly higher benefits.  But, the lack of an evidence base is hampering our ability to address these questions.  This favours the status quo, which could actually be doing more harm than good.

Finally, I can't help feeling the current direction of travel by Cochrane is taking us down a conceptual cul-de-sac [11]:

"Researchers in dominant paradigms tend to be very keen on procedure. They set up committees to define and police the rules of their paradigm, awarding grants and accolades to those who follow those rules. This entirely circular exercise works very well just after the establishment of a new paradigm, since building systematically on what has gone before is an efficient and effective route to scientific progress. But once new discoveries have stretched the paradigm to its limits, these same rules and procedures become counterproductive and constraining. That’s what I mean by conceptual cul-de-sacs."

Bottom line: Systematic reviews are vitally important in practicing evidence-based healthcare.  Given that there is a finite funding 'envelope' it is imperative to maximise the number of systematic reviews that can be undertaken and to maximise relevancy to clinical practice.  This means significantly reducing the cost per review and improving the prioritisation process.

References
  1. The Cochrane Oversight Committee. Measuring the performance of The Cochrane Library. 2012
  2. Allen IE, Olkin I. Estimating time to conduct a meta-analysis from number of citations retrieved. JAMA. 1999 Aug 18;282(7):634-5.
  3. Cochrane Collaboration Annual Report & Financial Statements 2010/11
  4. Payne D. Tamiflu: the battle for secret drug data. BMJ 2012;345:e7303
  5. HAI Europe - Dr. Tom Jefferson on lack of access to Tamiflu clinical trials
  6. Jefferson TO, Demicheli V, Di Pietrantonj C, Jones M, Rivetti D. Neuraminidase inhibitors for preventing and treating influenza in healthy adults. Cochrane Database Syst Rev. 2006 Jul 19;(3):CD001265
  7. Jefferson T, Jones MA, Doshi P, Del Mar CB, Heneghan CJ, Hama R, Thompson MJ. Neuraminidase inhibitors for preventing and treating influenza in healthy adults and children. Cochrane Database Syst Rev. 2012 Jan 18;1:CD008965. doi: 10.1002/14651858.CD008965.pub3
  8. Glasziou PP, Shepperd S, Brassey J. Can we rely on the best trial? A comparison of individual trials and systematic reviews. BMC Med Res Methodol. 2010 Mar 18;10:23. doi: 10.1186/1471-2288-10-23
  9. Hemens BJ, Haynes RB. McMaster Premium LiteratUre Service (PLUS) performed well for identifying new studies for updated Cochrane reviews. J Clin Epidemiol. 2012 Jan;65(1):62-72.e1
  10. Sagliocca L, De Masi S, Ferrigno L, Mele A, Traversa G. A pragmatic strategy for the review of clinical evidence. J Eval Clin Pract. 2013 Jan 15. doi: 10.1111/jep.1202
  11. Greenhalgh T. Why do we always end up here? Evidence-based medicine's conceptual cul-de-sacs and some off-road alternative routes. J Prim Health Care. 2012 Jun 1;4(2):92-7.J Prim Health Care. 2012 Jun 1;4(2):92-7.

07 marzo, 2012

Meta-analysis and New Knowledge

Cochrane Collaboration
Image via Wikipedia

Source: http://www.typepad.com/services/trackback/6a0120a692721d970b0120a90cc76f970b

When hierarchies of evidence are listed for the EBM world, meta-analyses of randomized trials generally sit at the pinnacle.
And yet, the actual meta-analyses that you encounter when researching a clinical question can be far less enlightening. Even if we grant a pass to the many systematic reviews at The Cochrane Collaboration that conclude with the a priori obvious fact that no high quality RCTs addressing a question have been performed, and another pass to the reviews that find a single RCT and publish its results as the results of the systematic review, we are still left with the innumerable meta-analyses that seem to provide less of a window on truth than the underlying trials.
Frequently such meta-analyses are either driven by the single large RCT that everyone would have cited anyway or, worse, a number of small, poorly-performed RCTs are combined with a moderate-sized, well-performed RCT and alter the results away from what was likely the best estimate of reality: the results of the well-performed RCT.
Meta-analysts often seem to either be too removed from their subject area and thus lack the expertise to really understand what went clinically right and wrong in the underlying RCTs (or be unwilling to use that knowledge to discriminate among the trials), or be too cozy with a single trial (typically as an author) and thus too willing to ding trials that found conflicting results.
Ultimately, meta-analysis only rarely seems to importantly advance our knowledge of an issue beyond where we would have found ourselves by just reading through the RCTs.
So with that background it is always interesting to me when a meta-analysis comes along that really seems to shed new light on a subject such that we seem to know something that we somehow didn't know when we just had the underlying trials.
An example came along in The Lancet last week.
Despite the enormous number of patients participating in randomized trials of statins, it has been uncertain what effect statins have on the development of diabetes. Some biochemical and animal studies suggested that statins might prevent diabetes. Clinical trials have been conflicting with some showing protection and other showing increased risk. In reviewing the underlying trials, it has been hard to figure out what is going on:
  • Are some statins protective while others are harmful?
  • Are hydrophilic statins having different effects than lipophilic statins?
  • Was the observation of increased diabetes risk in the JUPITER Trial just a random event that became noticeable because of reporting bias (where positive or interesting secondary outcomes are more likely to show up in a paper than negative results).
  • Are the varying results of the statin trials due to random variation around a single truth, or do the results suggest that the underlying trials differed from each other in some important way (perhaps because of the population studied, the way the statin was administered, or the way diabetes was assesses?
A month ago, anyone simply looking at the collection of trials would have had a hard time giving a coherent answer to the above questions. Now, after a nicely done meta-analysis by Prof. Naveed Sattar et al., there are reasonable answers to all these questions. And thinking about these questions also sheds light on how to read and judge a meta-analysis.
The new analysis found that patients treated with statins had about a 9% higher risk of diabetes than those treated with placebo or other agents. When I started reading the analysis, I had the questions in the list above already in mind and so was prepared to challenge the meta-analysis on several fronts. The authors of the analysis had appropriately anticipated my concerns and, to the extent the data allowed, answered them:
1) Was this really a chance finding driven by JUPITER? Before JUPITER found an increased risk of diabetes, there had been little discussion of statins and diabetes risk. JUPITER's findings could have been due to chance, but the publicity around the result could have triggered the meta-analysis. JUPITER was large enough to sway the results in the meta-analysis and perhaps lead to a self-fulfilling conclusion based in random variation. The meta-analysis, though, did a secondary analysis that excluded JUPITER, and found that the results were essentially the same.
2) Were the varying results in the trials due to random variation or true differences? The meta-analysis found little need to invoke anything more than randomness (as measured by a statistic called the I2). What had seemed to be conflicting results was likely nearly entirely due to random variation around a likely single true effect of slightly increased risk of diabetes.
3) Are some statins protective while others cause diabetes? The finding of little heterogeneity suggests the answer is no, but ultimately this is a hard question to answer definitively because of the more limited data about each individual statin. The meta-analysis found that the confidence intervals of the effects for individual statins overlapped such that it seemed unlikely that there were important differences among the statins, but it's hard to be certain. Additionally, lipophilic and hydrophilic statins showed the same effects on diabetes. And beyond that, the meta-analysis found that one of the main trials that had suggested a protective effect of pravastatin on diabetes had used an unusual definition of diabetes, and the effect was not seen when they substituted a standard definition.
While no new trials were published, as a result of this meta-analysis we have a much better feel for the effect of statins on diabetes than we had a few weeks ago. So, if after hours of trying to answer clinical questions by reading Cochrane you find yourself wondering whether meta-analyses are ever worth the effort that seems to go into them, remember this one and how much we learned about diabetes and statins from a new analysis of existing data.

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