Audit: QRS - Chinese Hawthorn for Health & Longevity

Audit conducted on 21/08/2026 12:21 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. 🟢 Spot-checked every span: protocol doses (ER 372, 374, 380, 384), time-to-effect (ER 429, 164), all 13 monitoring targets (ER 461–473), cadence (ER 455, 457, 473), 9 contraindications (ER 322, 336–348), 9 interactions (ER 314–332), benefit/risk tiers (ER 150–202, 222–294) and the qualitative list (ER 477–485).
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. 🟢 ER’s hedges are carried: “though trials disagree” mirrors ER 509; “claims rest on animals and cells” mirrors ER 509; “no reduction in cardiac events, with displacement risk” keeps the ER heading (ER 256).
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/breastfeeding stays an absolute contraindication; camphor stays an absolute contraindication (ER 322) rather than being demoted to 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. 🟢 Nothing from ER Benefit-Modifying Factors (ER 207–215) or Risk-Modifying Factors (ER 299–309) is surfaced in the gates or risk card; gates come only from ER Key Interactions & Contraindications.
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, no NCT identifiers, no author names, and no brand names (e.g., “Dr. Willmar Schwabe” from ER 378 is not surfaced).
1.6 The QRS does not introduce new attributions. 🟢 No attribution appears anywhere in 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. 🟢 The sheet reproduces the ER’s sceptical, species-aware framing (European relatives vs. Crataegus pinnatifida) without adding enthusiasm.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Quantified targets and explicit decision gates give the reader what is needed to act, while the evidence limits are stated plainly.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Every span is a noun phrase or descriptive statement; no prescriptive verbs.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Doses and thresholds are reported as what trials and pharmacopoeias used, not as instructions.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No occurrence of “recommend”, “advise”, “should”, or “we suggest” in any populated span.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns and no imperatives in any populated span.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Abbreviations from the ER table are expanded in full (LDL-C, HDL-C, ApoB, HbA1c, ALT, hs-CRP, NT-proBNP); the At-A-Glance uses “heart attacks”, “blood fats”, “mislabeled product”.
2.8 Information is presented in a concise and very compact manner 🟢 Every gate, benefit, risk, and monitoring entry is a single condensed phrase; no sentence-level prose outside the At-A-Glance and cadence line.
2.9 It DOES NOT address the reader directly 🟢 Confirmed across all populated spans.
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-optimal targets (e.g., triglycerides below 100 mg/dL, ALT below 20/17 U/L) rather than conventional disease cut-offs.
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. 🟢 Weekly home blood-pressure and pulse logging, a 13-marker panel, and split dosing with meals all assume a willing, effortful reader.
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. 🟢 The monitoring burden and the ApoB/NT-proBNP additions are well beyond general-population expectations.
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 displacement hazard and the species-mismatch problem are given weight proportionate to a self-directed supplement user.
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; the title uses “Health & Longevity”.
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. 🟢 “gastrointestinal complaints”, “myocardial infarction”, “orthostatic hypotension”, “phytobezoar” — clinical register throughout the card body.

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 verified at lines 446, 490, 536, 631, 661, 858, 567, 597; tier labels at 540/545/551/557 and 634/638/645/651; column headers at 665–667.
3.2 All “” from the [qrs_template] are present in the the QRS. 🟢 Full variable set present: page_title, header_topic, header_subline_date, header_subline_model, at_a_glance, action_1–3 (label/value/sub), time_1–3 (label/value/sub), benefits_×4, stop_items, caution_items, risks_×4, marker_1–13 (name/target/why), monitoring_cadence, qualitative_item_1–5.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 The non-variable template spans (website="evidence_review", website="full_review", website="audit"), the CSS block, and the footer disclaimer 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 ER section mapped onto the QRS is empty — Benefits, Risks, Interactions/Contraindications, Protocol, and Monitoring are all populated in the ER.
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 cells reuse ER bold labels verbatim: “Standardized extract, European model” (ER 372), “Whole-fruit, Chinese model” (ER 374), “Time of day” (ER 380); monitoring row labels reuse the ER table’s Biomarker column verbatim.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 No label is shortened or reworded; the only change is expansion of the ER’s abbreviations in the “Why” column, which is not a label.
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 tier emojis and “⚠️ Conflicted” markers are correctly dropped in favour of CSS palettes and bold tier labels.
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 entry is condensed to a single phrase and the template’s one-page layout (A4 @page rule, 9–11pt scale, two-column gates) is intact; content volume is the minimum the completeness items (8.2, 9.2, 14.2) permit.

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 and before the template comment on line 16.
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 --- on line 3, closing --- on line 13; the lead-in text on line 2 sits before 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. 🟢 Enclosed in an HTML comment; none of its values are repeated in the body except the creation date and model name, which are required by 6.3 and 6.4.
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: chinese_hawthorn_2026-0821-1033_Opus_ER.md — matches the ER on disk.
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: 2026-0821-1157.
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: qrs_filename: chinese_hawthorn_2026-0821-1033_Opus_QRS.html — matches 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. 🟢 Re-verified across all eleven 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: “Chinese Hawthorn for Health & Longevity - Quick Reference Sheet”, matching ER frontmatter 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: “Chinese Hawthorn for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “08/21/2026”, the correct reformat of 2026-0821-1157.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Line 425: “Opus 5”, matching the frontmatter.
6.5 No additional header content appears: no badge, version stamp, AKA / alternate names line, source-AI attribution, audit date, or QRS variant marker. 🟢 The header holds only the title and the template’s fixed subline; the ER’s “Also known as” list (ER 31) is correctly 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 ER 509–511 into the four decision-relevant facts: what is proven, in which species, how large, and where the real hazard sits.
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. 🟢 European relatives / exercise tolerance / no fewer events → ER 509; blood pressure and lipids → ER 509; animals and cells → ER 509; harms mild and the displacement and mislabelling hazards → ER 511.
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 Uses “heart attacks”, “blood fats”, “animals and cells”, “mislabeled product” — no acronyms, no clinical classifications.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial name, year, sample size, or p-value.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 Direction only (“falls modestly”, “improve”); no numbers.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All nine items trace to ER 312–348.
8.2 [stop_items] represent the Contraindications from the ER 🟢 All seven “Populations who should avoid” bullets (ER 336–348) are present, with ER 340 correctly split into two items, plus the camphor absolute contraindication (ER 322).
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Nine <li> elements, lines 570–592.
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 trailing rationales are stripped (“where symptom-level evidence cannot substitute for guideline therapy”, “until the cardiac regimen is stable”, “on preclinical uterine-stimulation data”); no dash-trailing clause survives.
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). 🟢 “NYHA Class IV”, “second- or third-degree”, “below 50 beats per minute”, “below 100 mmHg”, “within 90 days”, “(raw or dried whole fruit, not standardized extracts)”, “(apple, pear, peach, almond)” all preserved; only the ER’s plain-language glosses are dropped.
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 Key Interactions & Contraindications.
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 avoidance 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 nine items trace to ER 314–332.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Nine of the ER’s ten interaction bullets appear; the camphor bullet (ER 322) is correctly excluded because it sits in the Contraindications gate.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Nine <li> elements, lines 600–621.
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. 🟢 Each item is a bare noun phrase; the ER’s mechanism sentences and mitigation instructions (“Home pressure and pulse logging for 4 weeks manages it”, “a 7-day washout precedes elective surgery”) 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). 🟢 Named example drugs are carried from the ER bullet bodies: metoprolol/amlodipine/lisinopril/losartan, isosorbide mononitrate/sildenafil, warfarin/apixaban/clopidogrel, pseudoephedrine/phenylephrine, and the supplement and lifestyle lists.
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 Key Interactions & Contraindications.
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 ten 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 trace to ER Therapeutic Protocol (ER 370–394).
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 The two competing dose routes (ER 372, 374 — presented by the ER as alternatives at ER 376) and timing (ER 380) are the three load-bearing implementation decisions.
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. 🟢 Nine spans populated: 900–1,800 mg at 18.75% oligomeric procyanidins (ER 372); 9–12 g dried fruit as decoction, stir-fried slices, or granules (ER 374); with or just after the two largest meals, split two or three times daily (ER 380, 384).

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 🟢 Heart-failure symptoms, blood lipids, and blood pressure — the only three time-to-effect windows the ER states (ER 429, corroborated at ER 164).
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Heart failure is the ER’s only High-tier benefit (ER 150–152); lipids and blood pressure are Medium (ER 158–166), and are ordered as the ER orders them.
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; 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. 🟢 “8 weeks or later” and “8 to 16 weeks” come from ER 429; the triglyceride 12-week note from ER 164; the “not before 8 weeks” caveat from ER 429.
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 data at ER 429, so the section is correctly retained.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All four tiers map one-to-one onto the ER headings at ER 150–202.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present and populated, lines 538–560.
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 tier is a semicolon-joined list of the ER’s own benefit headings; no Magnitude figures (ER 156, 164, 170, 178, 184) are carried over.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any benefits span.
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 span needs hiding.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All four tiers map one-to-one onto the ER headings at ER 222–294.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present and populated, lines 633–655.
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 tier reproduces the ER’s risk headings only; the event counts and hazard ratios at ER 228, 234, 242, 248, 254, 260, 268, 274, 280 are all dropped.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any risks span; the ER’s glosses (“a spinning sensation”, “a hardened mass of plant fiber”) are stripped.
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 span needs hiding.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 The table reproduces the ER Monitoring Protocol & Defining Success biomarker table (ER 459–473).
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All thirteen ER rows are present in ER order, with targets and rationales carried across; abbreviations are expanded rather than dropped.
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 848–852 condense ER 455, 457 and the digoxin note at ER 473: baseline, weekly home readings, full panel at 12 weeks, then every 6 to 12 months.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 Taken from the ER’s “Qualitative markers worth tracking alongside the labs” list (ER 475–485).
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All five ER qualitative markers are present, verbatim and in ER order, at lines 861–888.

Issues 21/08/2026 12:21

Pass rate 100.00%. No issues found.

Issues 21/08/2026 12:09

  1. 12.3 / 13.3 — Conflicted qualifier not stripped: benefits_high (line 540), benefits_medium (line 546), and risks_medium (line 639) each end with a trailing “— conflicted” qualifier, which the section preambles declare redundant because the tier label already encodes evidence strength.

Fixes 21/08/2026 12:09

  1. 12.3 / 13.3 — Conflicted qualifier stripped: Removed the trailing “— conflicted” from benefits_high, benefits_medium, and risks_medium, leaving the tier label alone to carry the evidence-strength signal.

Issues 21/08/2026 12:07

  1. 1.3 — At-a-glance drops blood-pressure hedge: [at_a_glance] (line 435) asserts “Blood pressure falls modestly and blood fats improve”, while the ER Conclusion (line 509) qualifies it as “Blood pressure falls modestly, though the trials disagree”; omitting the hedge strengthens the ER claim.

Fixes 21/08/2026 12:07

  1. 1.3 — At-a-glance blood-pressure hedge restored: [at_a_glance] now reads “Blood pressure falls modestly, though trials disagree, and blood fats improve”, matching the ER Conclusion’s qualification; the closing clause was tightened to “replacing proven treatment” to keep the summary within the 60-word budget (now 59 words).