Audit: QRS - Hesperidin for Health & Longevity

Audit conducted on 22/09/2026 17:27 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 94
Passed 86
Failed 0
N/A 8
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. 🟢 Every span traced to ER text: protocol cells to Therapeutic Protocol (ER 356, 366, 368), time cells to Practical Considerations (ER 411) and Monitoring Protocol (ER 437), benefits/risks to the ER tier headings, gates to ER 311–334, monitoring rows to the ER biomarker table (ER 441–450).
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. 🟢 No cautious ER phrasing is hardened; speculative items (“Additive bleeding risk”, “Interference with drug metabolism via enzyme inhibition”) remain under the Speculative tier.
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”). 🟢 Avoid-list populations stay in the Contraindications gate and Caution/Monitor items stay in Key Interactions; no directional shift found.
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. 🟢 All eight caution items come from the ER Key Interactions & Contraindications bullets; no Benefit-Modifying Factors or Risk-Modifying Factors content appears in the gates.
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. 🟢 The QRS carries no PMIDs, citations, expert names, NCT identifiers, or brand names.
1.6 The QRS does not introduce new attributions. 🟢 No attributions present anywhere on the sheet.

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. 🟢 Lede mirrors the ER Conclusion register (“blood fats”, “blood sugar control”, “stomach upset”).
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Targets, thresholds and cadence are given without hedging or alarm.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Statements are descriptive (“Split dosing preferred above 500 mg/day”), not imperative.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No directives to the reader; the footer disclaimer is the template’s own.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No occurrences of “recommend”, “advise”, “you should” anywhere in the file.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns in the document.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical identifiers (OATP2B1, CYP3A4, eGFR, Child-Pugh) appear only in the decision gates, where item 9.5 requires them.
2.8 Information is presented in a concise and very compact manner 🟢 Gate and tier items are single clauses; monitoring “why” cells are one short phrase each.
2.9 It DOES NOT address the reader directly 🟢 Confirmed — no direct address anywhere in the sheet.
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. 🟢 Functional targets (LDL < 100 mg/dL, hs-CRP < 1.0 mg/L, HbA1c < 5.4%) are optimization-grade rather than disease-threshold values.
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. 🟢 Split dosing, meal timing, weekly home blood-pressure logging and a ten-marker panel all assume effort.
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. 🟢 No simplified or general-population framing; the sheet assumes baseline lab testing.
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. 🟢 The lede states benefit concentrates in people with an existing metabolic disorder, and marker 5 exists precisely to establish that status.
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. 🟢 “Longevity” appears only in the title/header from the ER canonical_topic; “anti-aging” does not appear.
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)”; “oral” / “administered orally” not “taken by mouth” / “given by mouth”; “injection” not “shot”; “adverse event” not “bad reaction”). This holds on EVERY surface, including the QRS lede — the stricter plain-language bar (see 2.7) does not license lay phrasing for route of administration. Direct quotes from sources are exempt. 🟢 Route and formulation are described formally (“purified hesperidin”, “with meals”, “gastrointestinal intolerance”); the lede’s plain terms reproduce the ER Conclusion wording.

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 strings byte-identical to the template (lines 446, 491, 540, 612, 637, 804, 573, 589, 641–643 and the four tier labels in both tiered cards).
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 Span-name diff against the template resolves cleanly: only marker_#_* → marker_1..10_* and qualitative_item_# → qualitative_item_1..5 row expansions.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 A full diff against the template shows changes only inside data-qrs-var spans and the metadata block; CSS, structure and the website= spans are 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. Typical phrasings are “None documented in human trials to date” and “Not formally studied” N/A No source ER section used by the QRS is empty.
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. 🟢 “Standard supplemental dose”, “Single versus split dosing” and “Best time of day” match the ER bold labels at ER 356, 366, 368 verbatim.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Protocol, time, tier and monitoring labels all reproduce ER wording.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 No emoji characters anywhere in the QRS; the ER’s tier emojis and “⚠️ Conflicted” markers were dropped.
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 reduced to bare facts — gate items are single clauses, tier lines carry no effect sizes, monitoring “why” cells are one phrase — while items 8.2, 9.2, 14.2 and 15.2 fix the row counts.

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, immediately after <!doctype html> on line 1.
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. 🟢 Opening --- at line 3, closing --- at line 13; the descriptive text sits on line 2.
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; none of its values are repeated in the header or body.
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. 🟢 Only duration: "00:03" is quoted, which the colon requires.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: er_filename: hesperidin_2026-0902-0001_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]” 🟢 Line 5: qrs_prompt_version: 26.9.22, matching the QRS.md version badge.
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” (e.g., 2026-0501-1430) 🟢 Line 6: qrs_creation_date: 2026-0922-1716.
5.8 The nickname of the AI used to create the document is stated as “qrs_creator_ai_nickname: [qrs_creator_ai_nickname]” 🟢 Line 7: 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) 🟢 “Opus” — 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]” 🟢 Line 8: 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) 🟢 “Opus 5” — nickname plus version, no qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9 matches the file’s own name on disk.
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. 🟢 Re-verified: every value is trimmed and unquoted except the colon-bearing duration.

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 &) 🟢 Line 22: “Hesperidin 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 (e.g., &amp; for &) 🟢 Line 417: “Hesperidin for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “09/22/2026” from qrs_creation_date: 2026-0922-1716.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Line 425: “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 holds only the title and the template subline; the ER’s “Also known as” line was not carried over.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] opens by saying what the intervention is — its kind (e.g., dietary supplement, prescription medication, peptide, plant, procedure, practice) — and what it is used for, in plain language, before any verdict on the evidence 🟢 Opens “the main plant compound in oranges and sold as a supplement for circulation and metabolic health” before any evidence verdict.
7.2 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Compresses all four ER Conclusion paragraphs (ER 482–486) into four sentences.
7.3 [at_a_glance] is no longer than 70 words 🟢 67 words.
7.4 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Traced to ER 37/39 (what it is and its use), 482 (lipids and vein symptoms), 484 (blood pressure, inflammation, glucose), 486 (stomach upset, microbial release, variability).
7.5 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “blood fats”, “blood sugar control”, “gut bacteria”, “active form” used in place of lipid, glycaemic, microbiome and aglycone terminology.
7.6 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial names, years, sample sizes or p-values.
7.7 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No numbers of any kind appear in the lede.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All six items come from “Populations who should avoid Hesperidin” (ER 327–334).
8.2 [stop_items] represent the Contraindications from the ER 🟢 All six ER avoid-list bullets are present, none added.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Six <li> elements inside the stop_items span (lines 576–584).
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. 🟢 ER rationale clauses (“given the theoretical antiplatelet effect”, “in whom clearance is unstudied”, “where supplemental doses have not been evaluated”) are all stripped; no trailing dash clauses remain.
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). 🟢 “platelets below 50 × 10⁹/L”, “Within 7 days”, “(Child-Pugh Class C)”, “(eGFR under 15 mL/min/1.73 m²)” and “beyond short-term third-trimester use” are all retained.
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. 🟢 The ER uses no ranking notation in this list; the only symbols retained are genuine numeric thresholds.
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 ER names six such populations and the section is correspondingly populated.
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 empty.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All eight items map to the ER interaction bullets at ER 311–325.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 All eight ER interaction bullets are present; the ER itself lists the narrow-therapeutic-index OATP2B1 case separately in the avoid list, so no duplicate is carried.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Eight <li> elements inside the caution_items span (lines 592–602).
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. 🟢 Caution/Monitor verdicts, mechanisms and mitigation sentences are stripped, as is the “which relax blood vessels to lower blood pressure” gloss on calcium channel blockers.
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). 🟢 Every ER example-drug parenthesis is preserved verbatim across all eight items.
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. 🟢 The ER parentheses are already plain comma-separated drug lists; no ranking symbols present.
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 ER names eight such interactions and the section is correspondingly populated.
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 empty.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 All three cells come from ER Therapeutic Protocol bullets (ER 356, 366, 368).
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Dose, dose splitting and timing — the three execution decisions; the form-specific and population-specific bullets are correctly left out.
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 more than three actionable aspects; 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 spans carry ER-derived content; no placeholder text remains.

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 🟢 Lipid/inflammatory, venous symptom relief and insulin/glucose — the three latencies the ER states (ER 411, 437).
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Lipids (High tier) → venous relief (High tier, listed second in the ER) → insulin and glucose (Low tier).
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 The ER supplies three distinct time-to-effect aspects; 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 spans carry ER-derived content; the subs quote the ER’s own latency wording.
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 provides time-to-effect information, so the section is correctly retained.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All thirteen entries correspond one-to-one with the ER Expected Benefits sub-headings (ER 155–229).
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated (lines 542–566).
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. 🟢 Each entry is the bare ER heading; all Magnitude lines and mechanism sentences are dropped.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses remain in any benefit tier.
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. N/A All four benefit tiers carry items in the ER.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All six entries correspond one-to-one with the ER risk sub-headings (ER 255–291).
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated (lines 614–631).
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. 🟢 Each entry is the bare ER heading; the relative risk 1.14, the Cochrane pooling and the fexofenadine figures are all dropped.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses remain in any risk tier.
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 items in the ER.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Rows and targets taken from the ER Monitoring Protocol & Defining Success table (ER 441–450).
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All ten ER table rows are present in ER order, from LDL cholesterol through body weight and waist circumference.
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. 🟢 Line 795: baseline, 12 weeks, 6 months, then annually, plus the weekly home blood-pressure logging for four weeks — matching ER 437.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 All five items come from the ER’s “Qualitative markers worth tracking alongside the labs” list (ER 454–458).
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five ER qualitative markers are present in ER order.

Issues 22/09/2026 17:27

Pass rate 100.00%. No issues found.

Issues 22/09/2026 17:21

  1. 1.3 / 2.5 — Imperative dosing instruction: Line 466 renders [action_2_value] as “Split above 500 mg/day”, an imperative that advises the reader and strengthens the ER’s “Split dosing is preferred above 500 mg/day” (ER line 366) into a directive.

Fixes 22/09/2026 17:21

  1. 1.3 / 2.5 — Imperative dosing instruction: Changed [action_2_value] from “Split above 500 mg/day” to “Split dosing preferred above 500 mg/day”, restoring the ER’s hedged framing and removing the imperative.