{
  "release_id": "2b2017b84496b985",
  "id": "cardio:bp-lowering-medicine",
  "owner": "cardio",
  "kind": "intervention",
  "slug": "bp-lowering-medicine",
  "name": "Blood pressure lowering medicine",
  "aliases": [
    "Antihypertensive medicine",
    "Antihypertensive drug treatment"
  ],
  "atlases": [
    "cardio"
  ],
  "summary_plain": "Medicines that lower blood pressure, started and adjusted for adults whose high blood pressure is confirmed.",
  "summary_technical": "Pharmacological antihypertensive treatment as framed by the WHO 2021 guideline: when to start (recommendation 1, three statements with different populations and strength labels), the first-line drug classes (recommendation 4) and combination therapy as initial treatment (recommendation 5). The classes are thiazide and thiazide-like agents, ACE inhibitors or angiotensin-receptor blockers, and long-acting dihydropyridine calcium channel blockers. Targets sit on the linked target record. Treatment steps in NICE NG136 were not read by this cluster. Each recommendation claim states its own population and strength label. One effect claim comes from a pooled analysis of 48 trials of blood-pressure-lowering medicines (BPLTTC, Lancet 2021), whose participants are not described as adults.",
  "editorial_state": "draft",
  "last_substantive_edit": "2026-10-12",
  "last_evidence_check": "2026-10-11",
  "next_review_due": null,
  "external_ids": [],
  "navigation": {
    "cardio": {
      "system": [
        "blood-vessels"
      ],
      "condition-area": [
        "hypertension"
      ]
    }
  },
  "payload": {
    "subtype": "medicine",
    "mechanism": null,
    "taxonomy_codes": []
  },
  "content_digest": "f947bed0fc70bce7efbead43c16b901af6ba7ade1dd96988fc0ae9e1266efb8b",
  "review": {
    "content_digest": "f947bed0fc70bce7efbead43c16b901af6ba7ade1dd96988fc0ae9e1266efb8b",
    "current": [],
    "conflicting": [],
    "stale": [],
    "inactive": []
  },
  "claims": [
    {
      "release_id": "2b2017b84496b985",
      "id": "cardio:claim-bplttc-mace-per-5mmhg",
      "owner": "cardio",
      "subject_entity_id": "cardio:bp-lowering-medicine",
      "category": "effect",
      "statement": "In a pooled analysis of individual-participant data from 48 randomised trials of blood-pressure-lowering medicines (344,716 people, median follow-up 4.15 years), a 5 mm Hg lower systolic blood pressure from treatment was associated with a lower risk of a major cardiovascular event: a stroke, a heart attack or ischaemic heart disease, or heart failure that caused death or needed hospital admission. The hazard ratio was 0.91 (95% CI 0.89 to 0.94) in people without previous cardiovascular disease and 0.89 (95% CI 0.86 to 0.92) in people with it. The authors report no reliable evidence that this proportional effect differed between the two groups.",
      "context": {
        "id": "cardio:ctx-bplttc-trial-participants",
        "label": "Participants in 48 randomised blood-pressure-lowering trials (BPLTTC 2021 meta-analysis)",
        "recipient": "unknown",
        "population": "People randomised in 48 trials of blood-pressure-lowering medicines, analysed in two groups: those with and those without previous cardiovascular disease, defined as stroke, myocardial infarction or ischaemic heart disease before randomisation. Mean age at baseline was 65 years in both groups. The age range is not reported in the text read, which does not describe the participants as adults, and it does not say how pregnancy was handled.",
        "care_setting": "Randomised clinical trials of blood-pressure-lowering medicines. The settings of the individual trials are listed in the paper's appendix, which was not read.",
        "geography": "Not stated in the text read (the trial list is in the appendix, which was not read)",
        "life_stage": "Not stated in the text read; mean age 65 years at baseline, age range not reported",
        "gestational_age_min_days": null,
        "gestational_age_max_days": null,
        "postnatal_age_min_days": null,
        "postnatal_age_max_days": null,
        "gestational_age_status": null,
        "postnatal_age_status": null,
        "followup_description": "Median follow-up of 4.15 years across the trials (Q1 to Q3 2.97 to 4.96 years).",
        "eligibility": {
          "inclusion": [
            "Trials that randomised people to blood-pressure-lowering medicines versus placebo or another class, or to more versus less intensive treatment",
            "Trials with at least 1000 person-years of follow-up in each randomised group",
            "Trials that shared baseline blood pressure, primary and secondary outcomes, and whether previous cardiovascular disease was present"
          ],
          "exclusion": [
            "Trials done only in people with heart failure",
            "Short-term trials in acute myocardial infarction or other acute settings",
            "People with known heart failure at baseline, in trials that had included them"
          ]
        }
      },
      "evidence_stage": "synthesis",
      "certainty": "not_assessed",
      "certainty_method": null,
      "limitations": "The pooled trials differ in design: placebo-controlled trials, comparisons of drug classes, and more-versus-less-intensive treatment. The hazard ratios are standardised to a 5 mm Hg systolic reduction, while the trials' average reduction between their groups, excluding the first 12 months, was 6.3 mm Hg. Previous cardiovascular disease means stroke, myocardial infarction or ischaemic heart disease before randomisation. Trials only in heart failure or acute settings, and people with known heart failure at baseline, are left out. The trials tested blood-pressure-lowering medicines in general, so the result is not specific to the first-line classes named in the WHO recommendations. The estimate is an average across trials. It says nothing about one drug or about benefit for one person. Each component outcome, stroke alone included, is shown in Figure 3 of the paper, an image that could not be read, so no component result is recorded here. The paper's Discussion also states a percentage reduction for each component, which comes from the same component results as Figure 3; those percentages are left unrecorded too, so this claim stays about the combined outcome. A two-stage sensitivity analysis gave similar estimates (0.89 with and 0.92 without previous cardiovascular disease). One erratum only updates the collaboration group list. The numbers are the authors' reported results, taken from the open-access PMC version rather than the publisher's version of record, and nobody has re-analysed them.",
      "editorial_state": "draft",
      "checked_at": null,
      "next_review_due": null,
      "valid_from": null,
      "valid_to": null,
      "citations": [
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}
