Question explored with the scientific record
In the uk there is a roll out in schools of the flu mist nasal spray. What long term tests have been done? How effective IS it as opposed to claims and how frequent are side effects
The flu mist is a live virus sprayed up the nose, and the evidence on its school rollout is thin on exactly the tests you would want: long-term safety studies comparing vaccinated to unvaccinated children.
The retrieval surfaced mostly short-term studies on small groups, animal models, or cost modeling. One study from England in 2015-2016 found that in vaccine-eligible children, getting the nasal spray cut the chance of being hospitalised with lab-confirmed flu by about 42% compared to unvaccinated children [3]. But the confidence interval on that number is wide: the true value could be as low as 7% or as high as 64% [3]. The same study found the injected flu vaccine was only about 29% effective, and that result was not even statistically significant — it could mean the shot did nothing [3]. Both of these are one-season numbers, not long-term.
For side effects, the only prospective safety trial in the retrieval tested just 48 children with asthma and found no significant lung function drop [1]. That is a tiny sample. A passive surveillance study from the US covering about 2.5 million doses logged 460 adverse event reports (40 serious), including 7 possible anaphylaxis cases and 2 cases of Guillain-Barre syndrome [7]. Passive systems like VAERS catch maybe 1% of real events, and they cannot tell you whether the rate is higher than what happens naturally. The same study noted that 73 of the 460 reports involved people who should not have been vaccinated at all (outside age range or with contraindicated conditions) [7]. The flu mist is a live virus, and in a few animal experiments, whole inactivated flu vaccines worsened lung disease on later infection with a mismatched strain — live vaccines did not have that problem in pigs [5], but the question of whether repeated annual boosting could narrow or misdirect immunity is largely unstudied in children over multiple years.
| Population | What was tested | Key result | Notes |
|---|---|---|---|
| Children 2-16, England, 2015-16 | LAIV (flu mist) vs unvaccinated [3] | 42% fewer flu hospitalisations | CI 7% to 64% |
| Children with asthma (n=48) [1] | LAIV vs placebo, lung function | No significant drop | Very small sample |
| ~2.5 million doses, US passive surveillance [7] | All reported events | 460 reports, 40 serious | Passive system misses most events |
| Pigs, heterologous challenge [5] | WIV vs LAIV | WIV worsened disease; LAIV did not | Animal model, not human |
My call: the flu mist probably reduces flu illness in the short term, but the long-term safety data on school-wide annual use in the UK does not exist in these records, and the side-effect rate in healthy children cannot be reliably estimated from the studies here.
Confidence: low, because the most informative study design (vaccinated versus unvaccinated over several years with full adverse event tracking) was not found.
Sources used 4
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Safety and tolerability of cold-adapted influenza virus vaccine in children and adolescents with asthma
A randomized, double-blind, placebo-controlled trial assessing the safety and tolerability of intranasal live attenuated CAIV-T influenza vaccine in children and adolescents with moderate to severe asthma, finding no significant adverse effects on lung function or exacerbations …
DOI: 10.1097/00006454-200201000-00010 -
Influenza vaccine effectiveness against hospitalisation due to laboratory-confirmed influenza in children in England in the 2015–2016 influenza season – a test-negative case–control study
In 2015-2016 England, influenza vaccination in vaccine-eligible children 2-16 years provided 33.4% adjusted effectiveness against laboratory-confirmed influenza hospitalisation, with LAIV at 41.9% and IIV at 28.8%.
DOI: 10.1017/s0950268819000876 -
Age at Vaccination and Timing of Infection Do Not Alter Vaccine-Associated Enhanced Respiratory Disease in Influenza A Virus-Infected Pigs
Whole inactivated virus (WIV) vaccination of pigs with a δ1-H1N2 (MN08) vaccine followed by heterologous pH1N1 (CA09) challenge induced vaccine-associated enhanced respiratory disease (VAERD) regardless of age at vaccination (4 or 9 weeks) or interval between boost and challenge…
DOI: 10.1128/cvi.00563-15 -
Adverse Events Reported Following Live, Cold-Adapted, Intranasal Influenza Vaccine
This study analyzes US VAERS data from 2003–2005 to characterize adverse events reported after intranasal live, attenuated influenza vaccine (LAIV-T), finding 460 reports (including 40 serious) among about 2.5 million vaccinees, with rare events such as possible anaphylaxis and …
DOI: 10.1001/jama.294.21.2720