Audit: QRS - Propolis for Health & Longevity

Audit conducted on 06/09/2026 03:49 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 values, time-to-effect figures, benefit/risk items, gate items, biomarker targets and cadence trace to ER Therapeutic Protocol, Practical Considerations, Expected Benefits, Potential Risks & Side Effects, Key Interactions & Contraindications and Monitoring Protocol & Defining Success.
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 ER section is empty and no cautious empty-state phrasing is misrepresented.
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”). 🟢 “Pregnancy and lactation” remains a contraindication, not a caution; tier assignments match the ER exactly.
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. 🟢 [stop_items] come from the ER “Populations who should avoid Propolis” list; [caution_items] from the eight ER interaction bullets; no Benefit- or Risk-Modifying Factor is surfaced.
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, author names or brand names (Apis Flora, EPP-AF®, Comvita) appear anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 No attributions of any kind are present.

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. 🟢 Flat, declarative, evidence-first register matching the ER throughout.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Quantified targets and doses paired with plain-language framing in At-A-Glance.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 No imperatives; content is stated as what the evidence shows.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Gate items are stated as conditions, not instructions; footer disclaimer is the template’s.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No occurrences of “recommend”, “advise”, or “should”.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns anywhere in the document.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms retained only where they are the biomarker or drug-class name; At-A-Glance is fully plain.
2.8 Information is presented in a concise and very compact manner 🟢 All benefit/risk items are heading-level; gate items carry no mechanistic rationale.
2.9 It DOES NOT address the reader directly 🟢 Confirmed by full-text scan for “you”/”your”/”we”/”our”.
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-range biomarker targets and blood-lead monitoring address exactly 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. 🟢 Twice-daily dosing, meal timing, weekly home blood pressure and annual blood lead are all presented without hedging on 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 simplification toward 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 states that changes are small where baseline numbers start good, which is the relevant caveat for this audience.
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. 🟢 “anti-aging” does not occur; “Modulation of aging hallmarks” uses the ER’s own wording.
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 throughout (“capsules”, “extract”, “glycated haemoglobin”); the plain-language wording 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 headings, gate labels, tier labels and table headers are byte-identical to the template.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 All 34 template variable names present; marker_#_* expanded to 8 rows and qualitative_item_# to 5 items as the template intends.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 <span website="evidence_review">, <span website="audit"> and <span website="full_review"> are unchanged; a structural diff against the template shows no markup or CSS changes.

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 that feeds 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. 🟢 “Standardized dry extract, oral”, “Metabolic protocol, higher dose”, “Best time of day” and all eight interaction labels are the ER’s bold labels verbatim.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Biomarker names and protocol labels match the ER; time-to-effect labels are drawn from the ER’s own “Time to effect” bullet wording.
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 “⚠️ Conflicted” marker on the COVID-19 benefit was 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. 🟢 Every section is condensed to headline level: benefits and risks carry no effect sizes or rationale, gate items carry no mechanism, protocol sub-lines are single clauses. No section carries elaboration that should have been cut.

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 “QRS — Metadata” caption precedes 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. 🟢 Fully enclosed in the HTML comment; no metadata value is repeated in the 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: propolis_2026-0906-0010_Opus_ER.md, matching the ER’s own filename frontmatter key.
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 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: 2026-0906-0335, correct format.
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 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” — nickname plus version number, no qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9: qrs_filename: propolis_2026-0906-0010_Opus_QRS.html, matching the file 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. 🟢 Confirmed for all nine keys; no stray whitespace or unnecessary 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: Propolis for Health &amp; Longevity - Quick Reference Sheet, matching ER canonical_topic with the ampersand 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 &) 🟢 Line 417: Propolis for Health &amp; Longevity.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: 09/06/2026, the correct MM/DD/YYYY rendering of 2026-0906-0335.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Line 425: Opus 5, matching the frontmatter value.
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 contains only the title and the template’s standard subline; the ER’s “Also known as” list is 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 🟢 Compresses all four Conclusion paragraphs — chemotype non-transferability, baseline-dependent benefit, allergy and lead, and the two mitigations.
7.2 [at_a_glance] is no longer than 60 words 🟢 59 words.
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Chemotype divergence and non-transfer, the four improved domains, the baseline caveat, permanent bee-product allergy, lead in raw material, and the skin-test/tested-product mitigations each map to a separate Conclusion or Sourcing passage.
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 Uses “blood sugar”, “blood fats”, “upper blood pressure”, “gum inflammation”, “hive resin”; no acronyms and no chemotype jargon.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial, author, year or sample size is named.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No numeric result appears.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Taken from the “Populations who should avoid Propolis” sub-list of that ER section.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All seven ER avoid-populations are present, in ER order.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Seven <li> elements inside the span (lines 572–581).
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 rationale “on absence of safety data rather than evidence of harm” is correctly stripped from the pregnancy item; no dash-trailing 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). 🟢 “(Asthma Control Test score below 15)”, “under 12 years”, “Within 7 days”, “on maintenance immunosuppression” and “(any concentration or source material)” are all preserved.
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 identifies seven such populations and the section is correctly populated rather than left empty.
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 🟢 Taken from the eight interaction bullets of that ER section.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 All eight ER interaction bullets present; none duplicates a contraindication item.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Eight <li> elements inside the span (lines 589–607).
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. 🟢 Every ER rationale clause (“additive glucose lowering with risk of hypoglycaemia”, “reduced clearance and raised drug levels”, the two-hour separation advice) is stripped; only the label and drug examples remain.
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). 🟢 All ER example drug lists are preserved, including the seven CYP substrates and the seven glucose/blood-pressure-lowering supplements.
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 identifies eight such interactions and the section is correctly 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 trace to the ER Therapeutic Protocol bullets.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Form/frequency, dose and duration, and dose timing — the three decisions a user must make before starting.
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 fields carry ER-derived content; no placeholders remain.

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 🟢 The ER’s “Time to effect” bullet names exactly three horizons — throat within 3 days, metabolic and inflammatory markers at 8–12 weeks, cognition at 12 months — and all three are carried.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Glycemic/lipid control is a High-tier ER benefit and leads; upper respiratory symptoms and cognitive scores are both Medium-tier and follow in ER order.
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 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 fields carry ER-derived content; the sub-lines add continuity, course length and the ER’s own caution that short trials prove little.
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 explicit time-to-effect information.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All 21 items are ER Expected Benefits sub-headings.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated: 5 High, 8 Medium, 4 Low, 4 Speculative — matching the ER tier counts exactly.
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 item is the bare ER heading; no magnitude figures, trial counts or mechanisms are carried across.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 “(Cold Sore)” is correctly stripped from the herpes labialis item; no parentheses remain in the section.
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 tiers contain items in the ER.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All nine items are ER Potential Risks & Side Effects sub-headings.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated: 1 High, 1 Medium, 3 Low, 3 Speculative — matching the ER tier counts exactly.
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. 🟢 The ER’s patch-test positivity rates, the 28%-vs-33% adverse-event figures and the 160 mg/kg lead ceiling are all correctly omitted.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content appears in any risk item.
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 tiers contain items in the ER.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Table and cadence both come from the ER Monitoring Protocol & Defining Success section.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All eight ER biomarker rows are present with targets and rationale reproduced verbatim: HbA1c, fasting insulin, hs-CRP, LDL cholesterol, triglycerides, ALT, home systolic blood pressure, blood lead.
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. 🟢 Reproduces the ER’s ongoing-testing paragraph: fasting glucose at 2 weeks on glucose-lowering medication, full panel at 12 weeks then every 6 months, weekly home blood pressure for 12 weeks, annual blood lead for continuous daily users.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Drawn from the “Qualitative markers worth tracking alongside the laboratory panel” list.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five ER qualitative markers are present, in ER order.

Issues 06/09/2026 03:49

Pass rate 100.00%. No issues found.

Issues 06/09/2026 03:41

  1. 12.4 / 2.15 — Parenthetical gloss kept, formal term dropped: In [benefits_medium] (line 545) the ER heading “Faster Healing of Herpes Labialis (Cold Sore) Lesions” became “faster healing of cold sore lesions”, preserving the parenthetical consumer-grade gloss instead of stripping it and keeping the formal term.

Fixes 06/09/2026 03:41

  1. 12.4 / 2.15 — Formal term restored in benefits: Changed [benefits_medium] from “faster healing of cold sore lesions” to “faster healing of herpes labialis lesions”, stripping the ER heading’s parenthetical gloss and keeping the formal term.