Audit: QRS - Elamipretide for Health & Longevity

Audit conducted on 30/08/2026 02:02 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 84
Failed 0
N/A 9
Pass Rate 100.00%
  • Total = Passed + Failed + N/A
  • Pass Rate = Passed / (Passed + Failed) × 100
  • N/A items are excluded from the pass rate calculation

1. General Rules

# Description Result Comments
1.1 Every claim, magnitude, label, recommendation, and statement in the QRS is literally supported by content in the source ER. 🟢 Spot-checked every populated span against the ER: protocol cells vs ER lines 334/336/342/346/356, time cells vs ER 153/393, benefit and risk items vs the ER tier headings, monitoring rows vs the ER biomarker table, qualitative items vs ER 435-439. All literally supported.
1.2 Where the ER uses cautious phrasing (“not formally studied”, “None documented in human trials to date”, “theoretical concern”, “data are limited”), the QRS uses the same phrasing. 🟢 Cautious ER phrasing carried over verbatim: “No circadian data exist”, “No age-, sex- or pharmacogenetic adjustment is specified”, “No established target”.
1.3 The QRS never strengthens an ER claim (e.g., “not formally studied” → “not required”) or softens one (e.g., “do not use during pregnancy” → “use with caution during pregnancy”). 🟢 No claim strengthened or softened; contraindications keep absolute framing, speculative tiers stay speculative.
1.4 The QRS does not relabel an ER fact under a different decision category. A “Benefit-Modifying Factor” from ER section is not surfaced as a “Caution”; a “Risk-Modifying Factor” is not surfaced as a “Side Effect”; etc. 🟢 Contraindications come from the ER’s “Populations who should avoid” list, interactions from the ER interaction bullets, risks from Potential Risks; no cross-category migration.
1.5 PubMed IDs, study citations, expert names, clinical trial identifiers (NCT*), and brand names appear in the QRS only if they appear in the source ER for the same fact. 🟢 No PMIDs, NCT identifiers, expert names or brand names (Forzinity/Bendavia) appear in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 No attributions introduced.

2. Focus, Tone & Audience

# Description Result Comments
2.1 The QRS follows the tone of the ER, which is determined by the ER’s own language, phrasing, and framing. 🟢 Matches the ER’s sober, skeptical register.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Expert, objective and data-driven; the deflationary emphasis mirrors the ER’s own conclusion rather than editorialising.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Presents evidence and thresholds; no prescriptive voice.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No imperatives or advice constructions; footer disclaimer intact.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 Information is stated, not recommended.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person address anywhere in the file.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms retained only where the decision gates require precision (drug names, biomarker names); at-a-glance uses plain language.
2.8 Information is presented in a concise and very compact manner 🟢 Compact throughout; sub-cells are one to three short sentences.
2.9 It DOES NOT address the reader directly 🟢 Confirmed: no “you”/”your” in the document.
2.10 The target audience is health- and longevity-oriented adults who are risk-aware, proactive, and actively seeking to optimize health or apply the intervention under review. 🟢 Content is pitched at a proactive, risk-aware longevity reader.
2.11 The target audience is willing to employ lifestyle and behavioral changes as well as follow protocols that may be inconvenient, costly, or require effort. 🟢 Daily subcutaneous injection, monitoring cadence and functional retesting are presented without hedging about inconvenience.
2.12 The document is NOT written for the general population, who are unwilling to employ lifestyle and behavioral changes or follow protocols that may be inconvenient, costly, or require effort. 🟢 Not framed for a general audience.
2.13 Framing, takeaways, and risk/benefit weighting throughout the document reflect this audience, including where an intervention’s signal for the average person differs from its signal for this audience. 🟢 Surfaces the longevity-relevant signals (aging-muscle energetics, speculative frailty/cognition) alongside the disease-population evidence.
2.14 The document’s own voice frames usage in longevity terms, not “anti-aging” (e.g., “anti-aging clinics”, “anti-aging community”, “anti-aging medicine”). Proper names that contain “anti-aging” (e.g., “American Academy of Anti-Aging Medicine”) are quoted verbatim. 🟢 No occurrence of “anti-aging”; the document uses “longevity”.
2.15 The document’s own voice uses formal clinical and scientific terminology, not colloquial or consumer-grade language (e.g., “oral medication” not “pill(s)”; “injection” not “shot”; “adverse event” not “bad reaction”). Direct quotes from sources are exempt. 🟢 Formal terminology in the document’s own voice; the plain-language phrasing in at-a-glance is required by item 7.4.

3. Template Integrity

# Description Result Comments
3.1 The following labels and headings on the QRS are fixed and not modified: Card and section headings: “Protocol”, “Time to effect”, “Benefits”, “Risk & Side Effects”, “Monitoring”, “Qualitative Assessment”; Gate headings: “Contraindications”, “Key Interactions”; Tier labels: “High”, “Medium”, “Low”, “Speculative”; Table column headers in Monitoring: “Marker”, “Target”, “Why” 🟢 All fixed headings, gate headings, tier labels and Monitoring column headers are byte-identical to the template.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 All 34 template variables present; verified by set comparison against the template (no missing, no extra).
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 The three website=”…” spans and all non-variable markup are unchanged; a structural diff against the template shows changes only inside variable regions.

4. Formatting

# Description Result Comments
4.1 When the source ER section is empty, the QRS uses the ER’s own empty-state phrasing verbatim. Typical phrasings are “None documented in human trials to date” and “Not formally studied” N/A No ER section mapped into the QRS is empty; the absent High benefit tier is governed by item 12.5, not by this item.
4.2 Where the ER presents a bulleted item as “Label: content”, the QRS uses the ER’s bold label verbatim as the cell or row label. 🟢 Protocol cell labels reuse the ER bold labels verbatim: “Standard approved regimen”, “Best time of day”, “Pre-existing conditions influencing response”.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 No ER label paraphrased or abbreviated. The Time-to-effect cell labels have no ER bold label to copy (the ER carries a single “Time to effect:” bullet), so they are derived, not substituted for an existing label.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 No emoji present; the ER’s tier emoji and the three “Conflicted” warning markers are stripped as required.
4.5 The QRS is designed to render on one A4 page. Any section that has more content in the ER than fits the per-section budget is condensed by the LLM, not extended onto a second page. 🟢 Each section is condensed to the template’s one-page budget; long ER cells (e.g. VO2peak target, 6MWD target) are trimmed rather than carried in full.

5. Metadata

# Description Result Comments
5.1 The metadata is placed inside a single HTML comment that is the first element after “<!doctype html>” and before any other comment, head, or body content. 🟢 The metadata comment is the first element after <!doctype html> (lines 2-14).
5.2 Inside that HTML comment the YAML block is delimited by a line “—” opening and a line “—” closing. Text before the opening “—” is permitted but is not parsed as YAML. 🟢 YAML opens at line 3 and closes at line 13; the preamble text sits before the opening delimiter.
5.3 The metadata is not visible in any rendered view of the QRS and is not surfaced by any other element on the sheet. 🟢 Enclosed in an HTML comment; not surfaced anywhere on the sheet.
5.4 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 All values trimmed and unquoted except duration, which contains a colon and is correctly quoted.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 er_filename: elamipretide_2026-0830-0015_Opus_ER.md.
5.6 Version of the QRS.md file used to create the document is stated as “qrs_prompt_version: [Version of QRS.md]” 🟢 qrs_prompt_version: 26.7.02, matching this QRS.md.
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” (e.g., 2026-0501-1430) 🟢 qrs_creation_date: 2026-0830-0144.
5.8 The nickname of the AI used to create the document is stated as “qrs_creator_ai_nickname: [qrs_creator_ai_nickname]” 🟢 qrs_creator_ai_nickname: Opus.
5.9 The nickname of the AI is just a single word model name without version, etc. (e.g., Opus, Sonnet, Grok, Gemini, ChatGPT) 🟢 Single word, no version.
5.10 The full name of the AI used to create the document is stated as “qrs_creator_ai_fullname: [qrs_creator_ai_fullname]” 🟢 qrs_creator_ai_fullname: Opus 5.
5.11 The full name of the AI consists of the [qrs_creator_ai_nickname] and the model version number and no additional qualifier (e.g., Opus 4.6, Sonnet 3.2, Grok 4.5, Gemini 3.1, ChatGPT 5.4) 🟢 Nickname plus version number, no qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 qrs_filename matches the actual filename.
5.13 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 As 5.4; frontmatter is clean and consistent.

6. Page Title & Header

# Description Result Comments
6.1 [page_title] is set to the [canonical_topic] of the ER frontmatter followed by “ - Quick Reference Sheet” (e.g., “Intervention - Quick Reference Sheet”). The [canonical_topic] is HTML-entity-encoded as needed (e.g., &amp; for &) 🟢 “Elamipretide for Health & Longevity - Quick Reference Sheet”, ampersand entity-encoded.
6.2 [header_topic] is set to the [canonical_topic] of the ER frontmatter, with HTML entities encoded as needed (e.g., &amp; for &) 🟢 “Elamipretide for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 08/30/2026, matching qrs_creation_date 2026-0830-0144.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Opus 5.
6.5 No additional header content appears: no badge, version stamp, AKA / alternate names line, source-AI attribution, audit date, or QRS variant marker. 🟢 Header is the unmodified template subline; no badge, AKA line or version stamp.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Condenses the ER Conclusion (lines 459-463) into an execution-oriented verdict.
7.2 [at_a_glance] is no longer than 60 words 🟢 Exactly 60 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Each of the six facts maps to a distinct ER conclusion passage (first approval / single ultra-rare indication / strongest results outside longevity / three larger trials missed / older-adult gain gone in a week / local injection-site harms).
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “mitochondria” is glossed as “cell power plants” in the same sentence.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial names, years or sample sizes.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No effect sizes or statistics.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Derived from the ER “Populations who should avoid Elamipretide” list inside Key Interactions & Contraindications (ER lines 305-312).
8.2 [stop_items] represent the Contraindications from the ER 🟢 All six ER contraindications are represented, one to one.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Six discrete <li> elements inside the [stop_items] span.
8.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 Every trailing rationale clause is stripped (e.g. “— an absolute contraindication with no rechallenge”, “because of benzyl alcohol toxicity”, “for whom no dose has been established”).
8.5 Parenthetical qualifiers from the ER bullet — time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 Qualifiers preserved: “under 2,500 g or under 34 weeks gestational age”, “under 30 kg”, “(eGFR under 30 mL/min)”, “cancer-free for under two years”.
8.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER uses no ranking notation inside parentheses in this section.
8.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no population, condition, or scenario for which the intervention should be avoided, deferred, or used only under specialist supervision. 🟢 The section is populated, and the ER does identify populations that must avoid the intervention.
8.8 If the section is left empty, an HTML comment inside the [stop_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not left empty.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Derived from the ER interaction bullets (ER lines 289-303).
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 All five ER bullets that describe an actual interaction or additive effect are carried; the three bullets the ER explicitly labels “no interaction” are correctly excluded, since listing them in a decision gate would contradict item 1.3.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Five discrete <li> elements inside the [caution_items] span.
9.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 Only the agent class survives; every “— caution, theoretical”, “— additive, effect unquantified” style clause and its rationale is stripped.
9.5 Parenthetical qualifiers from the ER bullet — example drug lists, time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 Named example drug lists preserved verbatim: (cimetidine, dofetilide), (non-steroidal anti-inflammatories, contrast dye, aminoglycosides), (valproate, phenytoin), (prednisone), (tacrolimus), (baclofen), (fexofenadine, cetirizine), (hydrocortisone).
9.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER uses no ranking notation inside parentheses in this section.
9.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no interaction, additive effect, or exposure that changes how the intervention is used. 🟢 The section is populated, and the ER does identify interactions that change how the intervention is used.
9.8 If the section is left empty, an HTML comment inside the [caution_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not left empty.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 Derived from the ER Therapeutic Protocol section (ER lines 332-356).
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 The dose regimen, the timing rule and the condition-driven dose adjustment are the three decision-bearing aspects; the competing-dose and split-dosing bullets are folded into the sub-cells rather than dropped.
10.3 If less that three distinct actionable implementation aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A The ER supplies well over three actionable aspects and all three sets are used.
10.4 All used [action_#label], [action#value], [action#_sub] items are filled with meaningful content derived from the ER Protocol section. 🟢 All nine action variables carry substantive ER-derived content.

11. Time to Effect

# Description Result Comments
11.1 The three sets of [time] items cover the three most important time-to-effect aspects from the ER 🟢 Kidney filtration, Barth functional gains and aging-muscle energetics are the three time-to-effect aspects the ER quantifies.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Ordered Medium tier (kidney oxygenation/filtration) first, then the two Low-tier items in the ER’s own Low-tier order (Barth strength/walking before short-term aging-muscle energetics).
11.3 If less that three distinct time-to-effect aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A Three distinct time-to-effect aspects exist and all three sets are used.
11.4 All used [time_#label], [time#value], [time#_sub] items are filled with meaningful content derived from the ER. 🟢 All nine time variables carry substantive ER-derived content.
11.5 If the ER does not provide any information on time to effect, the section is removed completely from the Protocol Panel N/A The ER does provide time-to-effect information, so the row is retained.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 Derived from the ER Expected Benefits section (ER lines 141-201).
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four benefit variables present.
12.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Items reduce to the ER tier headings; no magnitudes, mechanisms or study details carried.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content present.
12.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. 🟢 The ER records no High-tier benefit, and [benefits_high] is an empty span with style=”display: none” rather than empty-state text.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 Derived from the ER Potential Risks & Side Effects section (ER lines 219-267).
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four risk variables present.
13.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Items reduce to the ER tier headings; no frequencies or mechanisms carried.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content present.
13.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. N/A All four risk tiers carry at least one ER item, so no span needed hiding.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Derived from the ER Monitoring Protocol & Defining Success section (ER lines 419-431).
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All seven ER biomarker table rows are present, with targets and rationales matching the ER.
14.3 [monitoring_cadence] is populated with the monitoring cadence/frequency derived from the ER Monitoring section. It is not left with placeholder text or empty. 🟢 Populated from the ER cadence sentence at ER line 421.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Derived from the ER qualitative marker list (ER lines 433-439).
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five ER qualitative markers are listed.

Issues 30/08/2026 02:02

Pass rate 100.00%. No issues found.

Issues 30/08/2026 01:55

  1. 2.6 / 2.9 — Imperative addresses the reader: [marker_5_target] and [marker_6_target] (lines 706-708 and 724-727) read “track change from own baseline”, a bare second-person imperative; the ER’s own depersonalised wording is “track change from the individual’s own baseline” (ER lines 429-430).

Fixes 30/08/2026 01:55

  1. 2.6 / 2.9 — Reader-directed imperative removed: [marker_5_target] and [marker_6_target] were changed from “track change from own baseline” to “change from the individual’s own baseline”, restoring the ER’s depersonalised wording so neither target addresses the reader.

Issues 30/08/2026 01:50

  1. 4.2 / 4.3 — Protocol label abbreviated: [action_3_label] at QRS line 477 reads “Pre-existing conditions”, but the source ER bullet label at ER line 356 is “Pre-existing conditions influencing response:”; the label must be carried over verbatim, not truncated.

Fixes 30/08/2026 01:50

  1. 4.2 / 4.3 — Protocol label restored verbatim: [action_3_label] changed from “Pre-existing conditions” to “Pre-existing conditions influencing response”, matching the ER bullet label verbatim.