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Scene – Autumn 1953, West End theatre, final act.
Frisson of suspense ripples through audience.
Main protagonist: detective inspector. ‘Why haven’t I realised before?’
Injured victim: ‘Why didn’t you just open your eyes’.
Adversary-doppelgänger: Placing musket (softly but dramatically) on the floor.
‘So, you’ve finally foiled me. I thought that stating the obvious would throw you off the trail. Simple, but effective, knowing that you would doggedly follow instructions.’
Global child health: solar powered oxygen concentrators
Pneumonia is the largest cause of child deaths in low-income countries, and though still falling, the global burden is still around 800 000 per year, despite a steady decline since the introduction of S. pneumoniae and H. influenzae vaccination. Beside antibiotic resistance, lack of availability of oxygen in rural hospitals results in one of the major modifiable contributory factors. Trevor Duke and colleagues evaluated a programme for improving reliable oxygen therapy using oxygen concentrators, pulse oximeters and sustainable solar power in 38 remote health facilities in Papua New Guinea consisting of a quality improvement spoke, identification of gaps, problem solving and corrective measures. The concentrators were powered by solar panels, affording 3 days’ autonomy. The mortality incidence rate ratio in the post (2 to 4 years after the programme), pre (2–4 years before) postintervention was 0.60 (95 % CI 0.45 to 0.81), one of several favourable outcomes. The design (pre-post), of course, cannot account for other temporal changes but the beauty of the study is its simplicity: tapping into a natural resource (sunlight) that in PNG, like many peri-equatorial countries is constant and reliable. It is obvious that health facilities need a reliable source of power and oxygen to function, but as has been highlighted further in the COVID-19 pandemic, these can be scarce resources. See page 224
Cystic fibrosis (CF) screening
The CF blood spot screening programme has been an outstanding success. Screening largely consists of an immunoreactive trypsin, which, if high, is followed by DNA testing for CF transmembrane related mutations (IRT-DNAin Wales for example) and, in some guidelines (the rest of the UK) a further IRT if before the back up sweat test). Most CF NBS false negative cases are due to an IRT concentration below the screening threshold but, and here’s the so-obvious-that-we-didn’t-think-of-it twist, that the accuracy of IRT results is dependent on the quality of the dried bloodspot (DBS) sample. IRT concentrations in smaller DBS specimens (<8 mm diameter, <20 µL in volume) are up to 18% lower than those from correctly filled DBS specimen collection devices (10 mm mm diameter, ~50 µL volume). Iolo Doull and colleagues tested contributors of false negative results in Wales over the period 1996–2016 with robust numerator data. Over the era, of 673 952 infants screened, 239 were diagnosed with CF (incidence 1:2,819). The sensitivity of the programme was 0.96, and positive predictive value (as it should be in a screening programme) was 0.478. Eighteen potential false negatives were identified, eight of which were excluded (screened outside Wales, complex comorbidities or no identified CFTR variants of the 10 remaining false negatives, 9 (90%) had a low DBS IRT and at least one common CFTR variant and thus should have received a sweat test under the programme. DBS cards were examined for five of the nine false negative cases—all were classified as small/insufficient or poor quality. This study reaffirms the adage about ‘even the obvious needing to be stated at least once’. To my mind, this raises two immediate questions: shouldn’t the test taker (and this is easier said than done) be retaking those cards in which the diameter of the spot suggests inadequate sample volume (an extra heel prick but look at the dividends) and should the lab be analysing these ‘spots’ at all? See page 253
Overdiagnosis of pre-school obesity
‘No examination is complete without complete centile chart with standard deviation scores’ is the time-honoured shrill of the well-intentioned supervisor. No one would disagree in principle, but during an ongoing non-corona-related pandemic, obesity deserves re-examination. Why now? Because the ‘epidemic of obesity’ starting in infancy doesn’t quite ring true given the tendency to regress to the mean in young children and the natural increase in standard deviation (obese to thin cut offs) with age. Charlotte Wright’s persuasive Viewpoint argues the case for an alternative to the standard deviation centile +/-2 SD around the mean warning cut offs. The issues stem partly from the thresholds having on been extrapolated from adult high-risk standard deviations above the mean. This, though, doesn’t quite make sense: the trajectories are hard to predict, and BMI z score starts to change much later in childhood. The case is presented for the mathematically more stable in preschool children, relation (by percentage) of the median. Data from the Gateshead Millennium study (figure 1) demonstrate the differences: at the age of 2.5 years, the proportion above the 91st centile was around 25% while using the alternative approach where this cut off corresponds to a 120% median the proportion is only 6% (boys) and 8% in girls. This isn’t, of course, advocating for the abandonment of weight, height and BMI for the inherently more complicated, expensive and time consuming alternatives like skin fold thickness, bioimpedance, hydrogen labelled water or MR imaging for coelomic fat: these could be equally susceptible to the same issues with mean and SD. What is clear, though, is that one should understand the limitations of any tools (whether chart or lab test) is the context in which they should be interpreted. They are, after all, like everything in life, fallible. See page 212
Detective Inspector: ‘The clues were all there—how did I fail to see them?’
Curtain down, sustained applause. Voices of exiting theatre-goers fade into the night’s pea-souper.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent for publication Not required.
Provenance and peer review Commissioned; internally peer reviewed.
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