Audit: QRS - Agmatine for Health & Longevity

Audit conducted on 21/06/2026 04:19 using AI4L / Opus 4.8

Iterations

Summary

Items Count
Total 91
Passed 85
Failed 0
N/A 6
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. 🟢 All content traceable to ER.
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. 🟢 “experimental”, “unproven”, “unknown” mirror ER caution.
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”). 🟢 Contraindications/risks preserve ER strength.
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. 🟢 Categories map correctly to ER sections.
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 citations/IDs/names introduced.
1.6 The QRS does not introduce new attributions. 🟢 No new attributions.

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 ER objective tone.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Tone consistent.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Presents evidence, not orders.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Disclaimer present; no advice language.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 Informational framing throughout.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person address.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Plain language used.
2.8 Information is presented in a concise and very compact manner 🟢 Compact, single-page.
2.9 It DOES NOT address the reader directly 🟢 No “you”.
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. 🟢 Framing fits this audience.
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. 🟢 Consistent.
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 general-population framed.
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. 🟢 Weighting reflects audience.
2.14 The document’s own voice frames usage in longevity terms, not “anti-aging”. Proper names that contain “anti-aging” are quoted verbatim. 🟢 No “anti-aging” usage.
2.15 The document’s own voice uses formal clinical and scientific terminology, not colloquial or consumer-grade language. Direct quotes from sources are exempt. 🟢 Formal terminology used.

3. Template Integrity

# Description Result Comments
3.1 The following labels and headings on the QRS are fixed and not modified: card/section headings, gate headings, tier labels, Monitoring column headers. 🟢 Headings unchanged (“Risk & Side Effects” matches template).
3.2 All “” from the [qrs_template] are present in the QRS. 🟢 All template spans present (marker_#/qualitative_item_# rows expanded).
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 Unaddressed spans untouched.

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. 🟢 High benefit/risk tiers hidden via display:none, none empty-filled.
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. 🟢 Tier labels and markers preserved.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Labels intact.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). 🟢 No emoji in QRS.
4.5 The QRS is designed to render on one A4 page. Any section with more content than fits is condensed by the LLM, not extended onto a second page. 🟢 Content condensed to one page.

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. 🟢 Lines 2-14, first element.
5.2 Inside that HTML comment the YAML block is delimited by a line “—” opening and a line “—” closing. 🟢 Delimited correctly.
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. 🟢 Inside HTML comment.
5.4 All frontmatter values are trimmed: no leading/trailing whitespace, no surrounding quotes unless required by YAML. 🟢 duration quoted (colon); others clean.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 er_filename: agmatine_2026-0621-0250_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: 26.5.18
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” 🟢 qrs_creation_date: 2026-0621-0250
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. 🟢 “Opus”.
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 4.8
5.11 The full name of the AI consists of the nickname and the model version number and no additional qualifier. 🟢 “Opus 4.8”.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 qrs_filename: agmatine_2026-0621-0250_Opus_QRS.html
5.13 All frontmatter values are trimmed: no leading/trailing whitespace, no surrounding quotes unless required by YAML. 🟢 Values clean.

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”. The [canonical_topic] is HTML-entity-encoded as needed. 🟢 “Agmatine for Health & Longevity - Quick Reference Sheet”.
6.2 [header_topic] is set to the [canonical_topic] of the ER frontmatter, with HTML entities encoded as needed. 🟢 “Agmatine for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 “06/21/2026”.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 “Opus 4.8”.
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 clean.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Distills Conclusion (lines 419-423).
7.2 [at_a_glance] is no longer than 60 words 🟢 54 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 All facts traceable to Conclusion.
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 Plain-language only.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial citations.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No statistics.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Derived from “Populations who should avoid agmatine” (line 278).
8.2 [stop_items] represent the Contraindications from the ER 🟢 All four populations represented.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Four <li> items.
8.4 Items are as concise as possible. No trailing explanations, mechanistic rationale, attributions, citations, study details, or content after a dash. 🟢 Clean; ER parentheticals (“no safety data” etc.) dropped.
8.5 Parenthetical qualifiers from the ER bullet — time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item. 🟢 “symptomatic hypotension”, “poorly controlled”, “intensive glucose-lowering therapy”, “significant” preserved.
8.6 When the ER uses ranking notation inside parens (e.g., “>”) that depends on an explanatory phrase, normalize to a plain comma-separated list. N/A ER contraindications use no ranking notation.
8.7 If no [stop_items] are present the section is left empty N/A Contraindications are present.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Derived from interaction bullets (lines 266-276).
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Six interaction items; no contraindication duplication.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Six <li> items.
9.4 Items are as concise as possible. No trailing explanations, mechanistic rationale, attributions, citations, study details, or content after a dash. 🟢 Concise; severity/consequence/mitigation 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. 🟢 Drug classes/example supplements preserved (alpha-2 agonists, ACE inhibitors, ARBs, beta-blockers; insulin, sulfonylureas, metformin; etc.).
9.6 When the ER uses ranking notation inside parens (e.g., “>”) that depends on an explanatory phrase, normalize to a plain comma-separated list. N/A ER interactions use no ranking notation.
9.7 If no [caution_items] are present the section is left empty N/A Interactions are present.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 From Therapeutic Protocol (lines 298-323).
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Studied dose, lower/nootropic range, timing & dosing.
10.3 If less than three distinct actionable implementation aspects are mentioned, unused sets are left empty/invisible. N/A Three aspects present.
10.4 All used [action_#label], [action#value], [action#_sub] items are filled with meaningful content derived from the ER Protocol section. 🟢 All filled from Protocol.

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 🟢 Two aspects exist in ER; both shown, third hidden.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Neuropathic pain (Medium) before Mood/Nootropic (Low).
11.3 If less than three distinct time-to-effect aspects are mentioned, unused sets are left empty/invisible. 🟢 time_3 set to display:none, empty.
11.4 All used [time_#label], [time#value], [time#_sub] items are filled with meaningful content derived from the ER. 🟢 Filled from Practical Considerations (line 353).
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 ER provides time-to-effect information.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 From Expected Benefits (lines 142-190).
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four present (high hidden).
12.3 Items are as concise as possible. No explanations, effect sizes, qualifiers, attributions, citations, study details, or mechanistic explanations. 🟢 Subsection headers only.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheticals carried over.
12.5 If no items of a specific sub-section are present the respective is set to “display=none”, not filled with empty-state phrasing. 🟢 benefits_high set display:none (no High benefits).

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 From Potential Risks (lines 206-248).
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four present (high hidden).
13.3 Items are as concise as possible. No explanations, effect sizes, qualifiers, attributions, citations, study details, or mechanistic explanations. 🟢 Subsection headers only.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheticals carried over; “⚠️ Conflicted” qualifier on Blood Pressure Lowering correctly dropped.
13.5 If no items of a specific sub-section are present the respective is set to “display=none”, not filled with empty-state phrasing. 🟢 risks_high set display:none (no High risks).

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 From Monitoring Protocol table (lines 381-387).
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All five (BP, fasting glucose, HbA1c, eGFR, VAS) listed with ER targets.
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. 🟢 Cadence from line 379.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 From qualitative bullets (lines 391-395).
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five qualitative markers listed.

Issues 21/06/2026 04:19

Pass rate 100.00%. No issues found.

Issues 21/06/2026 04:12

  1. 11.3 — Time set 3 placeholder text: The third time-to-effect set retains raw template placeholders “[time_3_label]”, “[time_3_value]”, and “[time_3_sub]” (lines 505, 508, 511) and the surrounding .pcell is not made invisible; the ER provides only two distinct time-to-effect aspects, so the unused third set should be emptied and hidden.

Fixes 21/06/2026 04:12

  1. 11.3 — Unused time set hidden: Emptied the placeholder text from the third time-to-effect set (time_3_label, time_3_value, time_3_sub) and added style="display:none" to its .pcell, since the ER provides only two distinct time-to-effect aspects.