Research findings — patterns the topline numbers obscure
This page surfaces structural patterns the topline numbers obscure. All charts are descriptive of the case-record dataset; each cited case links to its source decision. The patterns are observed in published Special Master rulings — not vaccine-safety claims.
The 4-tier compensation gating system
Compensation rates aren't a single distribution — they are four structural regimes. Conditions that fit "adult-style autoimmune" legal labels (Tier 1) compensate at 80–95%. Pediatric brain-injury labels off the Vaccine Injury Table (Tier 2) compensate at roughly half that rate. Autism-spectrum filings (Tier 3) compensate at 0% on the merits. The HPV-dysautonomia / POTS cluster (Tier 4) compensates at near-zero.
Open
Adult-style autoimmune labels with the strongest Althen track records or a Vaccine Injury Table presumption. SIRVA and post-flu GBS dominate the volume.
Gated
Pediatric brain-injury labels off the Vaccine Injury Table. Compensable in principle, but onset windows, alternative-cause challenges, and high evidentiary thresholds gate the rate.
Closed (autism docket)
Autism-spectrum filings compensate at 0% on the merits. The non-zero number reflects 42 U.S.C. § 300aa-15(e)(1) fee-only awards on petitions dismissed for insufficient causation.
Closed (HPV-dysautonomia cluster)
HPV-dysautonomia / POTS / small-fiber-neuropathy cluster. The Office of Special Masters has consistently rejected the underlying causation theories; compensable cases are isolated.
Each tier groups multiple condition categories; the per-condition breakdown drills into individual rates.
Same court, same statute, 60-point spread
Pediatric brain-injury compensation rates by Special Master, restricted to cases under conditions where the alleged injury includes encephalopathy, seizure disorder, developmental delay/regression, autism-spectrum, or CDD. Each Special Master hears the same docket of filings; case-mix differences do not explain the full spread.
The highest-rate Special Master compensates these cases at 65%; the lowest at 0% — a 65-point spread on essentially the same body of pediatric brain-injury claims.
Filing strategy matters: which Special Master a case is assigned to is one of the strongest individual-case predictors of outcome. Each judge's full docket is on their profile page.
The petitioner-counsel firm effect
The same statute applies regardless of who represents the petitioner. In practice, specialist firms (Conway-Homer-Chin-Caplan, Maglio Christopher & Toale, Kraus Law Group, Robert J. Krakow PC) compensate pediatric brain-injury claims at 70–75%, while pro-se filings — petitioners who could not retain specialist counsel — compensate at 0% across the corpus we sampled (n=31 pro-se).
The Vaccine Act reimburses petitioner attorneys' fees on dismissed petitions filed in good faith with reasonable basis (42 U.S.C. § 300aa-15(e)(1)), so specialist firms can afford to litigate uncertain causation theories without exposing the family to costs. Less experienced counsel and pro-se filers face the same evidentiary and procedural rules but without the institutional knowledge of which framings, experts, and Special Masters produce favorable outcomes for a given clinical picture.
This is one of the multi-layer access-to-counsel asymmetries that stratify outcomes in a no-fault federal compensation program. The Special Master profile pages show the per-master docket and comp rate; the autism-spectrum condition page documents the 0% on-the-merits rate that pro-se filers face.
How the genetic-vulnerability defense became a doctrine — then got reversed
The Vaccine Injury Compensation Program's evidentiary regime has shifted in identifiable phases. The shift most relevant to pediatric brain-injury and autism-spectrum cases is the rise (2010-2012) and partial appellate reversal (2022-2025) of the "genetic vulnerability defeats causation" framework.
- 1986 — National Childhood Vaccine Injury Act creates the program. Althen v. HHS later codifies a 3-prong causation test for off-Table claims.
- 1993 — Suel v. HHS: DPT-aggravation of pre-existing tuberous sclerosis paid — precedent for vaccine aggravation of genetic syndromes, 15 years before Hannah Poling.
- 2008 — Hannah Poling — HHS concedes Table encephalopathy in a child with mitochondrial dysfunction. Visible watershed for the modern doctrine.
- 2009-2010 — Cedillo, Snyder, Hazlehurst — OAP Theory 1 test cases denied. King, Mead, Dwyer — OAP Theory 2 test cases denied 2010-03-12. Categorical autism rejection takes effect.
- 2010-2012 — Hammitt, Barnette — SCN1A / Dravet defense framework crystallizes. Pediatric seizure cases with identified genetic mutations begin losing routinely.
- 2022 — Federal Circuit / CFC vacates the SM denial in L.M. (DYNC1H1 mutation): "Special Master improperly assumed injury was purely genetic." Direct appellate authority that the categorical genetic-defense framework cannot be used as a categorical bar.
- 2022 — Federal Circuit / CFC vacates and remands H.H. (Aicardi-Goutières Syndrome / Type I interferonopathy): "diagnosis of AGS was arbitrary and capricious because it did not adequately consider vaccine aggravation."
- 2024-2025 — Compensated post-genetic-defense cases stack: K.S.J. Jr. ($1.62M, MMR + SLC19A3 activation), J.C.T. ($2.22M, Pentacel + GABRA1 / Dravet), Weaver/T.M. ($1.63M, DTaP + pre-existing developmental delays). Federal Circuit reversal in Weaver: "Court of Federal Claims reversed — improperly elevated the burden of proof."
- 2025 — The 2025 Hazlehurst Rule 60(d) opinion acknowledges DOJ's expert "had expressed to DOJ attorneys that vaccines could cause autism in a subset of children with mitochondrial dysfunction" — same biology that paid Hannah Poling. The court calls the distinction "procedurally distinct."
The pattern is documented in autism-spectrum, seizure disorder, encephalitis/encephalopathy, and developmental delay/regression condition rosters. The Special Masters who decided the foundational denials (Hastings, Vowell, Lord) and the reversals (post-2018 Federal Circuit panels) are profiled in Special Master directory.
Same vaccine, same age window, opposite outcomes
Curated cohort of post-MMR pediatric neurological-injury cases at the 12–20 month age window. All involve post-vaccination neurodevelopmental injury. The variable that flipped each outcome was the legal label the petition was filed under — not the underlying clinical picture.
| Petitioner | Age | Filed as | Outcome | Award | Year |
|---|---|---|---|---|---|
| William Yates Hazlehurst | 12 mo | autism (OAP test 3) | DISMISSED | — | 2025 |
| A.E. | 144 mo | ADEM | WON | $3.1M | 2025 |
| O.G.R. | — | encephalopathy | WON | $2.5M | 2018 |
| Y.Q. | 15 mo | seizure + sensory + behavioral | WON | $2.0M | 2020 |
| M.W. | 20 mo | Pentacel encephalopathy + later ASD diagnosis | WON | $1.9M | 2018 |
| Eilise Moriarty | 48 mo | encephalopathy + cognitive/motor decline | WON | $1.6M | 2018 |
| R.B.M. | — | encephalitis (alternative: autism, denied) | WON | $969K | 2013 |
| V.S.R. | 14 mo | encephalitis (death) | WON | $310K | 2025 |
| M.P. | 12 mo | ADEM + transverse myelitis | WON | $166K | 2024 |
| S.D. | 12 mo | encephalitis (treating MD: 'autistic regression — MMR') | WON | — | 2024 |
Source: public Special Master decisions in the U.S. Court of Federal Claims, Office of Special Masters. Cohort selected from the analysis batches by the registry maintainer; all listed cases link to their original decisions.
Frequently asked questions about the VICP
General questions about the U.S. Vaccine Injury Compensation Program.