Audit: QRS - Young Plasma Transfusion for Health & Longevity

Audit conducted on 22/09/2026 20:00 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 94
Passed 83
Failed 0
N/A 11
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. 🟢 Protocol cells trace to ER lines 351–355; time-to-effect cells to ER lines 384 and 408; benefits/risks to the ER tier headings; at-a-glance to ER Conclusion lines 485–491.
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. 🟢 “Laboratory measures only; no recovery benefit shown” mirrors ER line 155; “Harms are well characterized” mirrors ER line 489.
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”). 🟢 All contraindication thresholds and time windows carried at ER strength; ACE inhibitors retained as a contraindication, not downgraded to a caution.
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 “Populations who should avoid” list plus the ER’s explicit absolute contraindication; interactions from the ER interaction bullets.
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, PMIDs, NCT IDs or expert names appear; drug names in the gates are the ER’s own generic-name examples.
1.6 The QRS does not introduce new attributions. 🟢 No attributions 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. 🟢 Measured, sceptical register matches the ER throughout.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Thresholds and targets are given plainly without alarm or advocacy.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Content is stated as evidence and reference values, not instruction.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No imperatives directed at a reader; monitoring cadence is descriptive of the ER protocol.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No recommending or advising verbs used.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns anywhere in the rendered content.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Immunoglobulin, apheresis and clock terms are unavoidable and match the ER; at-a-glance is jargon-free.
2.8 Information is presented in a concise and very compact manner 🟢 Every gate, benefit and risk item is reduced to the bare fact.
2.9 It DOES NOT address the reader directly 🟢 Confirmed: no direct address.
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. 🟢 Framed for elective, self-directed use, consistent with the ER’s framing.
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. 🟢 Retains cost/invasiveness and full apheresis monitoring schedule without simplification.
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. 🟢 Assumes access to laboratory panels and a specialist procedure.
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 foregrounds the removal-versus-addition distinction that matters for an elective purchaser.
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. 🟢 “marketed for longevity”; the term “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 is given as “infusing”, “infusion”, “exchange” and “apheresis”; the one informal phrase (“drugs that ride on plasma proteins”) is the ER’s own bold label reproduced verbatim per 4.2.

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 unchanged at lines 440, 477, 519, 539, 556, 576, 595, 599–601, 736 and in the tier list items.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 All 34 template variables present; marker_#* and qualitative_item# expanded to 11 and 6 instances respectively.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 Diff against the template shows changes confined to the metadata block and the variable spans; the three website= spans and all CSS 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 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. 🟢 Protocol labels and all eight interaction labels reproduce the ER bold labels verbatim.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Time-to-effect labels are drawn from the ER’s own phrasing at lines 384 and 408.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 No emoji in the file; 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. 🟢 Every section is reduced to minimal ER-derived phrasing; the remaining volume is driven by items 8.2, 9.2, 14.2 and 15.2, which mandate the full gate, biomarker and qualitative lists.

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 the doctype.
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 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: "00:02" 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: young_plasma_transfusion_2026-0815-0808_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 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: 2026-0922-1949.
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.
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” carries no additional qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9 matches the actual filename 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 across all nine 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: “Young Plasma Transfusion 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, correctly entity-encoded.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “09/22/2026” from 2026-0922-1949.
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” list 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 “is a procedure infusing the liquid part of blood from young donors into older adults, marketed for longevity” before any evidence verdict.
7.2 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Compresses all four Conclusion paragraphs (ER lines 485–491).
7.3 [at_a_glance] is no longer than 70 words 🟢 69 words.
7.4 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Small trials in dementia/Parkinson’s → line 485; removal beats addition → line 487; harms well characterized → line 489; expensive/invasive/uninsured → line 491.
7.5 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; plasma is glossed as “the liquid part of blood”.
7.6 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial named.
7.7 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No numeric results present.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Drawn from ER lines 301 and 315–325.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All nine “populations who should avoid” entries plus the ACE-inhibitor absolute contraindication are present.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Ten <li> elements, lines 542–551.
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. 🟢 Trailing rationales (“in whom no safety data exist”, “in whom alloimmunization can prolong waiting time”, “mirroring the exclusion criteria applied in every trial”) all stripped.
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). 🟢 7 mg/dL, NYHA III–IV, EF below 30%, 90 days, CKD stage 4, eGFR below 30, fibrinogen below 1.5 g/L, 5 years and the 24-hour window 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 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. N/A The section is 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 populated.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Drawn from ER lines 297–313.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 All eight non-contraindication interaction bullets present; ACE inhibitors correctly excluded and placed in the Contraindications gate.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Eight <li> elements, lines 559–566.
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. 🟢 The ER’s em-dash glosses (“— blood thinners”, “— laboratory-made antibody drugs”) and all mechanistic rationale are 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). 🟢 Every ER example-drug list is carried through intact.
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. N/A The section is 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 populated.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 Derived from ER Therapeutic Protocol lines 351–355.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 The ER’s three named approaches — whole plasma infusion, plasma exchange with albumin, plasma protein fractions — are the ER’s own top-level protocol bullets.
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 Three distinct aspects exist 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 cells carry ER-sourced dosing, schedule and donor-age detail.

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 three components of the ER’s own “Time to effect” bullet (line 408), with the durability note corroborated at line 384.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Clock-based change (ER Medium tier) first, protein/immune signalling (ER Low tier) second, loss of effect last.
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 cells carry ER-sourced timing and qualification.
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 at line 408.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 Derived from ER lines 143–185.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present at lines 521–532.
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 ER benefit heading alone; the ⚠️ Conflicted markers, magnitudes and sponsor attributions are all dropped.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content remains in any benefit entry.
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 has no High-tier benefit; line 521 sets style="display: none" with no empty-state text.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 Derived from ER lines 209–277.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present at lines 578–589.
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 ER risk heading alone; per-unit rates and the ⚠️ Conflicted marker are dropped.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content remains in any risk entry.
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 ER risk tiers contain items, 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 table, lines 438–450.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All 11 ER biomarker rows are reproduced with their optimal ranges and rationales intact.
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 730 reproduces the ER’s schedule from line 436 (pre-exchange draws, 4 weeks, 3 months, 6-monthly, serology at 3 and 6 months).

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Derived from the ER qualitative-marker list, lines 454–459.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All six ER qualitative markers present verbatim at lines 739–754.

Issues 22/09/2026 20:00

Pass rate 100.00%. No issues found.

Issues 22/09/2026 19:51

  1. 11.4 — Time-to-effect subs duplicate values: time_1_sub (“Measurable at one to two months”, line 489) and time_2_sub (“Appear within days of infusion”, line 500) are word-for-word restatements of time_1_value and time_2_value, so two of the six Time-to-effect cells carry no information.

Fixes 22/09/2026 19:51

  1. 11.4 — Time-to-effect subs duplicate values: Replaced time_1_sub “Measurable at one to two months” with “Composite biological age fell after plasma exchange” and time_2_sub “Appear within days of infusion” with “Laboratory measures only; no recovery benefit shown”, so both cells add ER-supported information instead of restating their value.