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The edition · Paediatrics

Prophylactic dextrose gel does nothing for school-age cognition and may cost something else, while a single RSV antibody dose covers a whole season

Seven-year follow-up of the hPOD trial finds no cognitive benefit from prophylactic buccal dextrose gel and a signal of worse emotional-behavioural outcomes; clesrovimab matches monthly palivizumab with one dose; a maternal high egg and peanut diet does not prevent infant allergy; and a point-of-care alert held a stewardship gain for two years after the teaching stopped.

The edition in brief

School-age follow-up of the hPOD trial assessed 1,067 New Zealand children at 6 to 7 years who as at-risk newborns received a single 0.2 g/kg buccal dose of dextrose gel or placebo at one hour of age. Neurocognitive impairment was 59% with dextrose gel and 57% with placebo (adjusted risk difference 3%, 95% CI -3% to 9%). Among eleven exploratory outcomes, emotional-behavioural difficulty was more common with dextrose gel (24% vs 18%, aRD 7%, 95% CI 1-12) as was low psychosocial function (17% vs 12%, aRD 6%, 1-10). The SMART trial randomised 997 palivizumab-eligible infants to a single 105 mg dose of clesrovimab or up to five monthly palivizumab doses: adverse events were comparable, and RSV-associated medically attended lower respiratory infection through day 150 was 3.2% versus 3.4%; a 210 mg dose before a second season was well tolerated, with 7.3% incidence through day 180. PrEggNut randomised 2,137 pregnant women at high familial allergy risk to a high or standard egg and peanut diet; infant IgE-mediated egg or peanut allergy at one year was 7.8% versus 8.4% (RR 0.93, 95% CI 0.69-1.26). A paediatric network sustained short-course prescribing for skin and soft tissue infection at 88.5%, up from 62.5%, for 21 months after active teaching ended, using a point-of-care alert alone. A Medicaid cohort of 36,552 sepsis episodes found 30-day mortality of 3.9% with wide regional variation.

In this edition
01
Clinical update

One clesrovimab dose matched five monthly palivizumab injections, and a second-season dose was tolerated

Where a long-acting RSV monoclonal is available, one dose a season replaces five monthly injections at comparable safety and comparable infection rates.

2 min · JAMA pediatricsRead →
Primary outcome
proportion of participants experiencing adverse events in season 1
Effect
adverse events comparable between groups; RSV-associated medically attended lower respiratory infection 3.2% (95% CI 1.8-5.2) vs 3.4% (2.0-5.6) through day 150; second-season 210 mg dose tolerated, 7.3% (4.4-11.4) through day 180
02Research

Loading the maternal diet with egg and peanut did not prevent infant allergy

Advise normal maternal intake of egg and peanut; the prevention that works is timely introduction to the infant at weaning.

2 min · The New England journal of medicineRead →
03Clinical update

A point-of-care alert held a prescribing gain for 21 months after the teaching stopped

Build the reminder into the prescribing step rather than into the teaching; the alert, not the education, is what held this gain for two years.

2 min · PediatricsRead →
04Research

Paediatric sepsis mortality varied more across regions than illness severity explains

Familiarity with paediatric sepsis appears to be protective; where there is a choice, send the child to the unit that sees them most often.

2 min · PediatricsRead →
05Pearl

Treat a low point-of-care glucose in a symptomatic newborn before the laboratory confirms it

Act on the point-of-care glucose in a symptomatic newborn and send the laboratory sample at the same time; never let the confirmation delay treatment.

1 minRead →
06
Practice changer

Prophylactic dextrose gel: no cognitive benefit at 6 to 7 years, and a signal in the wrong direction

Stop prophylactic dextrose gel in at-risk normoglycaemic newborns; it did not protect cognition at school age and may have cost something.

2 min · JAMA pediatricsRead →
Primary outcome
neurocognitive impairment at 6-7 years, defined as more than 1 SD below the normative mean on 1 or more of 7 NIH Toolbox items
Effect
59% vs 57% (adjusted risk difference 3%; 95% CI -3% to 9%; P = .36); exploratory: emotional-behavioural difficulty 24% vs 18% (aRD 7%; 1-12) and low psychosocial function 17% vs 12% (aRD 6%; 1-10)

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