Audit: QRS - Chaste Tree for Health & Longevity

Audit conducted on 16/08/2026 12:04 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 83
Failed 0
N/A 10
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 protocol, time, benefit, risk, gate, marker and qualitative content traces to the ER (Therapeutic Protocol, Practical Considerations, Expected Benefits, Potential Risks & Side Effects, Key Interactions & Contraindications, Monitoring Protocol & Defining Success, Conclusion).
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. 🟢 Speculative tiers are carried as “Speculative”; no cautious ER wording is upgraded.
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”). 🟢 Absolute contraindications stay in the stop gate; caution-level interactions stay in the caution gate.
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. 🟢 Modifying-factor bullets are not used anywhere; each gate/tier item comes from the matching ER section.
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. 🟢 Only Ze 440 and BNO 1095 appear (line 457), both from the ER Therapeutic Protocol bullet for the same dose fact; no PMIDs, NCT IDs or author names.
1.6 The QRS does not introduce new attributions. 🟢 No attributions of any kind in the QRS.

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. 🟢 Wording is largely ER-verbatim, including the Conclusion’s own register in At-A-Glance.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Objective and specific throughout, with actionable protocol and monitoring targets.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Content is stated as evidence and targets, not as instructions to a patient.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No prescriptive second-person constructions; cadence and gates are stated descriptively.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No “recommended”, “advised” or “should” constructions in the QRS body.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns anywhere in the file; the ER’s imperatives (“Rate”, “Record”, “Log”) were converted to nominal forms in the Qualitative Assessment card.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms carry the ER’s own glosses (“Ferritin (the stored form of iron)”, “thyroid-stimulating hormone”).
2.8 Information is presented in a concise and very compact manner 🟢 Every item is reduced to its key fact; magnitudes, citations and mechanistic rationale are stripped.
2.9 It DOES NOT address the reader directly 🟢 Confirmed by full-text scan for you/your/we/our — no hits.
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. 🟢 Baseline biomarker panel, functional target ranges and a defined three-cycle trial address an active self-optimizing 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. 🟢 Seven-marker baseline panel and daily symptom tracking assume high willingness to act.
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. 🟢 Content depth (extract identity, mid-luteal timing, LH-to-FSH ratio) is beyond general-population framing.
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. 🟢 At-A-Glance retains the sponsor-bias and overstated-effect caveat rather than a promotional summary.
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” is used in the title; “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)”; “injection” not “shot”; “adverse event” not “bad reaction”). Direct quotes from sources are exempt. 🟢 Clinical register throughout (“intermenstrual bleeding”, “hypersensitivity skin reactions”, “mid-luteal progesterone”); no consumer-grade substitutions.

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 present verbatim (lines 446, 493, 542, 573, 590, 621, 649, 653–655, 774) and all four tier labels appear in both Benefits and Risks.
3.2 All “” from the [qrs_template] are present in the the QRS. 🟢 61 named spans present with unbroken numbering (action 1–3, time 1–3, marker 1–7, qualitative 1–6) plus the three website= template spans at lines 423, 426, 440.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 The website="evidence_review", website="audit" and website="full_review" spans are untouched; every named span is covered by a checklist item.

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 relied on 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 European protocol”, “Best time of day”, “Baseline biomarkers”, and all six Qualitative Assessment labels match the ER bold labels verbatim.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Marker names match the ER biomarker table verbatim; Time-to-Effect labels are drawn from the ER’s own benefit headings and cycle-regulation wording.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 Full-text scan returns no emoji code points; the ER’s ⚠️ Conflicted markers were correctly 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 the minimum permitted by the completeness requirements of 8.2, 9.2, 12.2, 13.2, 14.2 and 15.2; no residual explanations, magnitudes or citations remain to condense.

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.
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; no duplicate of these values appears in head 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, correctly, because it contains a colon.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: er_filename: chaste_tree_2026-0825-1111_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: 26.7.02, matching 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) 🟢 Line 6: qrs_creation_date: 2026-0816-1156.
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” is a single word with no version or qualifier.
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” is nickname plus version with no qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9 matches the file on disk: chaste_tree_2026-0825-1111_Opus_QRS.html.
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. 🟢 Confirmed across all eleven keys; no stray whitespace or quoting.

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: “Chaste Tree for Health & Longevity - Quick Reference Sheet”, matching ER canonical_topic.
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: “Chaste Tree for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “08/16/2026”, matching qrs_creation_date: 2026-0816-1156.
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 (lines 415–428); the ER’s “Also known as” line was not carried over.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Lines 434–438 compress all three Conclusion paragraphs: mechanism, evidence tiering, safety, and sponsor bias.
7.2 [at_a_glance] is no longer than 60 words 🟢 58 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Each clause maps to a distinct Conclusion sentence (ER lines 471, 473, 475).
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “prolactin” is glossed as “the milk-producing hormone” and “second-half hormone patterns” replaces “luteal phase”.
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 numeric results; the effect is described qualitatively as “probably overstated”.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All seven items map to the ER’s “Populations who should avoid Chaste tree” list (ER lines 314–320).
8.2 [stop_items] represent the Contraindications from the ER 🟢 All seven ER avoid-populations are present; none is omitted or added.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Seven <li> elements inside the span (lines 576–585).
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. 🟢 The ER’s post-em-dash rationale (“theoretical uterine-stimulant… no human safety data”, “prolactin suppression may reduce milk supply”) is stripped; only applicability qualifiers survive.
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). 🟢 “larger than 10 mm”, “active or in remission”, “at least four weeks beforehand” and “under 18 outside specialist supervision” 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. N/A The ER uses no ranking notation 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 ER names seven such populations and the section is populated accordingly.
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 seven items map to the ER’s interaction bullets (ER lines 296–310).
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Seven of the ER’s eight interaction bullets appear; “Ovulation-induction and assisted reproduction drugs” is correctly excluded because it is an absolute contraindication carried in [stop_items].
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Seven <li> elements inside the span (lines 593–611).
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. 🟢 All “Caution.” sentences and mechanism text are stripped, including the ER’s “which supplies L-DOPA” gloss and “where sold without prescription” qualifier.
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 agents are retained for every item (haloperidol/risperidone/amisulpride/metoclopramide, bromocriptine/cabergoline, cimetidine/promethazine, Mucuna pruriens/vitamin B6/zinc, Hypericum perforatum).
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 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 ER names eight interactions and the section is populated accordingly.
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 derive from the ER Therapeutic Protocol bullets (ER lines 344, 352, 364).
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Dose/extract identity, dose timing, and baseline biomarkers are the three load-bearing implementation decisions in that section.
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 at least three distinct 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 spans carry ER-derived content (lines 450–488); the sub-cells reproduce the ER’s extract names, timing rationale and baseline panel.

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 🟢 Premenstrual symptoms, cyclical breast pain and cycle regulation, drawn from ER Practical Considerations and the breast-pain magnitude data.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Order follows the ER benefit tiers: two High-tier benefits first, then the Low-tier cycle-irregularity benefit.
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 spans populated (lines 499–534); “3 cycles”, “3 cycles” and “Up to 6 months” all trace to ER statements.
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 (ER line 399), so the section is correctly retained.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All eight benefit headings from the ER are represented in the matching tier.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated (lines 544–566).
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. 🟢 Items are the ER benefit headings only; the Magnitude paragraphs (responder rates, SMD 0.67, RR 2.57) are all excluded.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses in any benefit item; the ER’s “⚠️ Conflicted” markers are also dropped.
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 The ER populates all four benefit tiers, so no sub-section is empty.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All nine risk headings from the ER are represented in the matching tier.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated (lines 623–643).
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 are the ER risk headings only; the Magnitude paragraphs and Daniele/Schellenberg citations are excluded.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses in any risk item; the ER’s “⚠️ Conflicted” marker on Acne is dropped.
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 The ER populates all four risk tiers, so no sub-section is empty.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Rows reproduce the ER Monitoring Protocol & Defining Success biomarker table, including its “Why Measure It?” text.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All seven ER biomarkers present: prolactin, mid-luteal progesterone, TSH, estradiol, LH/FSH, ALT and ferritin, with their optimal functional ranges unchanged.
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. 🟢 Lines 764–768 carry baseline, three-cycle, six-month, six-to-twelve-month intervals plus the earlier-retesting triggers from ER line 425.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 All six items come from the ER’s “Qualitative markers worth tracking” list (ER lines 439–449).
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 Premenstrual symptom diary, breast comfort, cycle regularity, sleep quality, energy and cognitive clarity, and skin — six of six, with the ER’s bold labels intact.

Issues 16/08/2026 12:04

Pass rate 100.00%. No issues found.