In the second blog of our new series Understanding Evidence, Iain Chalmers, our founding director, looks at developments in research on prenatal corticosteroids since the work which gave rise to the Cochrane logo. Join in the conversation on Twitter @iainchalmersTTi @CochraneUK #understandingevidence.
The birth of the Cochrane logo
Twenty four summers ago I asked David Mostyn to design a logo to illustrate the objectives of the soon-to-be-opened Cochrane Centre. He did a good job: the circle reflects global objectives and international collaboration; the mirror image ‘Cs’ stood for the Cochrane Centre (and, a year later, the Cochrane Collaboration); the horizontal and vertical lines show the results of some early Randomization is the process of randomly dividing into groups the people taking part in a trial. One group (the intervention group) will be given the intervention being tested (for example a drug, surgery, or exercise) and compared with a group which does not receive the intervention (the control group). More Clinical trials are research studies involving people who use healthcare services. They often compare a new or different treatment with the best treatment currently available. This is to test whether the new or different treatment is safe, effective and any better than what is currently used. No matter how promising a new treatment may appear during tests in a laboratory, it must go through clinical trials before its benefits and risks can really be known. More assessing the effects of prenatal corticosteroids on the likelihood of early neonatal death More; and the diamond is a statistical summary of the information derived from the individual studies above it. As prenatal corticosteroids were not in widespread use at the time, the logo illustrated the human costs that can result from failure to prepare systematic, up-to-date reviews of A trial in which a group (the ‘intervention group’) is given a intervention being tested (for example a drug, surgery, or exercise) is compared with a group which does not receive the intervention (the ‘control group’). More of health care.
The story of prenatal corticosteroids has been documented in a Wellcome Trust Witness Seminar: among other contributions, Patricia Crowley, an Irish obstetrician, described her initial In systematic reviews we search for and summarize studies that answer a specific research question (e.g. is paracetamol effective and safe for treating back pain?). The studies are identified, assessed, and summarized by using a systematic and predefined approach. They inform recommendations for healthcare and research. More of controlled trials of prenatal corticosteroids, and I described how the Cochrane logo came to be designed. At the inaugural Cochrane Colloquium in 1993, Andrew Herxheimer presented the directors of the four Cochrane Centres and their administrator colleagues with wrist watches with faces based on the Cochrane logo (mine is still going strong).
Over subsequent years, the Cochrane logo has gradually achieved iconic status and become very widely associated with independently prepared, high quality systematic reviews of research evidence. Patricia Crowley’s original review (1) was first updated and extended by Devender Roberts and Stuart Dalziel in 2006 (2) [Stuart works at the same Auckland, New Zealand, hospital at which the first, ground-breaking trial of steroids had been done and reported in 1972 (3)]. Prophylactic prenatal corticosteroids became very widely adopted, particularly after they were endorsed in the early 1990s at a consensus conference organised by the Office of Medical Applications of Research of the US National Institutes of Health. And in 2012 and 2013, the UN Commission on Life Saving Commodities and Save the Children both recommended rapid, worldwide ‘scale up’ of prenatal corticosteroids (4).
Might prenatal corticosteroids actually be harmful?
This widespread consensus was challenged in 2014 when Kishwar Azad and Anthony Costello fired a warning shot in a Lancet commentary (4) entitled ‘Extreme caution is needed before scale-up of antenatal corticosteroids to reduce preterm deaths in low-income settings.’ They warned about the dangers of using steroids without adequate ‘level 2’ neonatal care, and referred to alarming evidence in populations in which the The proportion of a population who have a particular condition or characteristic. For example, the percentage of people in a city with a particular disease, or who smoke. More of malnutrition and the A way of expressing the chance of an event taking place, expressed as the number of events divided by the total number of observations or people. It can be stated as ‘the chance of falling were one in four’ (1/4 = 25%). This measure is good no matter the incidence of events i.e. common or infrequent. More of sepsis are high and access to antibiotics is low.
The ‘alarming evidence’ to which Azad and Costello referred was published in The Lancet on 14 February 2015. Fernando Althabe and his many colleagues published a large randomised cluster trial done to assess the effects of a multi-faceted A treatment, procedure or programme of health care that has the potential to change the course of events of a healthcare condition. Examples include a drug, surgery, exercise or counselling. More designed to increase the use of prenatal corticosteroids at all levels of health care in low-income and middle–income countries. The results did not endorse the message that had been conveyed in the Cochrane logo and in the 2006 version of the relevant Cochrane Reviews are systematic reviews. In systematic reviews we search for and summarize studies that answer a specific research question (e.g. is paracetamol effective and safe for treating back pain?). The studies are identified, assessed, and summarized by using a systematic and predefined approach. They inform recommendations for healthcare and research. More (2). Instead, the new An investigation of a healthcare problem. There are different types of studies used to answer research questions, for example randomised controlled trials or observational studies. More estimated that for every 1000 women exposed to the steroid use scale up strategy, there was an excess of 3.5 neonatal deaths and increased maternal infection (6), and secondary analysis suggests that this increased mortality was attributable to differential exposure to prenatal steroids (7).
This information is clearly of immense importance. As of 2016, an update of the relevant Cochrane Review was in progress with the Cochrane Pregnancy and Childbirth Group (7). However, the trial reported by Althabe et al. (5) did not actually meet the criteria for inclusion in the update. This is because it is not an evaluation of the effects of steroids – an intervention of establish benefit – but rather an evaluation of the effects of an intervention to scale up the use of prenatal steroids (Zarko Alfirevic, personal communication).
WHO’s prompt response to important new evidence
WHO responded promptly to the new evidence by amending its preterm birth guidelines: these now state that steroids should be used only when an accurate assessment of gestational age is available; when preterm birth is considered imminent; when there is no evidence of maternal infection; and in circumstances where adequate childbirth and neonatal care is available.
WHO has also sponsored a new trial comparing steroids with An intervention that appears to be the same as that which is being assessed but does not have the active component. For example, a placebo could be a tablet made of sugar, compared with a tablet containing a medicine. More in women at high risk of preterm birth between 26 and 33 weeks gestation in level 2 hospitals in low-income and middle-income countries (Fernando Althabe, personal communication). It will clearly be important for the updated Cochrane review to refer to this study.
As Kathy Burgoine and her colleagues in Uganda wrote in response to the report by Althabe and his colleagues:
To ensure that every neonate who might benefit from antenatal corticosteroids does, great urgency is now needed to clarify in which neonates these drugs will be beneficial. Antenatal corticosteroids might have no role in settings of high-infective illness or harm More, alternatively it could be that for these drugs to be beneficial they need to be given in conjunction with antibiotics and other infection control measures. (8)
But antibiotics may cause, as well as reduce, problems. Routine administration of antibiotics before membrane rupture in preterm labour may indeed reduce the number of women who develop infections; but this policy may also result in an increase in neonatal deaths and enduring functional impairment (9). As suggested by Azad and Costello (4), drugs alone are unlikely to meet the needs of childbearing families in low-income and middle-income countries.
When should a Cochrane systematic review be regarded as ‘closed’?
In 2015, Yves Lacasse and his colleagues in the Cochrane Airways Group declared that their review of the effects of pulmonary rehabilitation in A health condition marked by long duration, by frequent recurrence over a long time, and often by slowly progressing seriousness. For example, rheumatoid arthritis. More obstructive pulmonary disease was closed because the results, based on 65 controlled trials, had become ‘stable’ (10): further updating was highly unlikely to modify its relevance for the foreseeable future (measured in years rather than months). Their review thus would now seem to provide a solid basis for informing practice and policy, and for challenging any proposals to do yet more trials addressing the same question as likely to be unethical and a waste of precious resources (www.ebrnetwork.org).
The Cochrane Review of corticosteroids for women at risk of preterm birth (2) confirmed in 2006 that research done over the three previous decades had validated the message conveyed fourteen years earlier in the Cochrane logo. Not unreasonably, some people may have concluded that the issue had been settled and that the review should now be regarded as ‘closed’, not in need of any further updating, and should influence policy worldwide. The findings reported by Fernando Althabe and his colleagues (6) have reminded us that things are not quite as simple as they may once have seemed to have been.
The continuing evolution of evidence about the effects of prenatal corticosteroids is simply the most recent illustration of the importance of confronting the daunting challenge of providing up-to-date, reliable evidence of the effects of health care.
James Lind Initiative
1 September 2016
I am grateful to Zarko Alfirevic, Fernando Althabe, John Castle and Jack Leahy for comments on an earlier draft of this commentary.
Iain Chalmers has nothing to disclose.
In 2020, the Cochrane Review “Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth” was updated. Studies from low‐ and medium‐resource settings were added and the conclusions were strengthened:
“Evidence from this updated review supports the continued use of a single course of antenatal corticosteroids to accelerate fetal lung maturation in women at risk of preterm birth. Treatment with antenatal corticosteroids reduces the risk of perinatal death, neonatal death and RDS and probably reduces the risk of IVH. This evidence is robust, regardless of resource setting (high, middle or low).”