# 2024 Thai guidelines on the treatment of hypertension

**Authors:** Sirisawat Kunanon, Praew Kotruchin, Pairoj Chattranukulchai, Chavalit Chotruangnapa, Weranuj Roubsanthisuk, Prin Vathesatogkit, Tada Kunavisarut, Songkwan Silaruks, Sirakarn Tejavanija, Tuangsit Wataganara, Piengbulan Yapan, Nijasri Suwanwela, Pongamorn Bunnag, Buncha Satirapoj, Surapun Sitthisook, Rapeephon Kunjara Na Ayudhya, Apichard Sukonthasarn

PMC · DOI: 10.2478/abm-2025-0034 · Asian Biomedicine: Research, Reviews and News · 2025-12-31

## TL;DR

The 2024 Thai hypertension guidelines update diagnostic thresholds and treatment strategies based on global evidence and local clinical practices.

## Contribution

Introduces a new 'BP at risk' category and emphasizes out-of-office blood pressure measurements for more accurate hypertension diagnosis.

## Key findings

- The 'BP at risk' category (130–139/80–89 mmHg) was added to identify individuals at higher risk of hypertension.
- Out-of-office BP measurements like HBPM and ABPM are recommended to confirm hypertension diagnosis.
- Combination therapy in one pill is advised for most patients, except for specific low-risk or elderly groups.

## Abstract

The committee of the 2024 Thai Guidelines on the Treatment of Hypertension has reviewed new developments in the body of knowledge, combined with expertise in real-life clinical practice and evidence collected from clinical studies worldwide. The Guidelines consist of newly highlighted key topics to be up to date and suitable for the country’s context. We still maintained the current office blood pressure (BP) cut-point of 140/90 mmHg for hypertension diagnosis. The new BP category, “BP at risk,” i.e., BP of 130–139/80–89 mmHg, was introduced. The out-of-office BP measurements, including home BP monitoring (HBPM) or ambulatory blood pressure monitoring (ABPM), are also advocated to confirm the diagnosis of hypertension. Target BP levels depend on the age of the patients i.e., 120–130/70–79 mmHg for patients age 18–65 years, 130–139/70–79 mmHg for patients over 65 years of age. There are 5 main groups of antihypertensive medication, that is, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, betablockers, calcium-channel blockers, and diuretics (thiazides and thiazide-like diuretics such as chlorthalidone and indapamide). Two types of medications should be started for most patients, except for frail elderly patients, patients with relatively low initial BP (140–149/90–99 mmHg), and low-risk patients; only 1 type of starting medication should be selected. Medication that is a combination of 2 types in 1 pill should be selected. Patient empowerment can be useful in sharing decisions in goal setting, provision of feedback channels, self-monitoring, education, and motivation, which the use of telemedicine and mobile health technologies can assist.

## Full-text entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}
- **Diseases:** hematoma (MESH:D006406), autonomic failure (MESH:D012791), metabolic syndrome (MESH:D024821), syncope (MESH:D013575), arterial diseases (MESH:D002539), fibrosis (MESH:D005355), cerebral hypoperfusion (MESH:D002547), headaches (MESH:D006261), sarcopenia (MESH:D055948), inflammation (MESH:D007249), papilledema (MESH:D010211), acute coronary 1 syndromes (MESH:D054058), dyslipidemia (MESH:D050171), fluid (MESH:D002559), hyperkalemia (MESH:D006947), DM (MESH:D003920), aortic dissection (MESH:D000784), atherosclerotic renovascular disease (MESH:D014652), electrolyte abnormalities (MESH:D014883), anxiety (MESH:D001007), CKD (MESH:D051436), Preeclampsia (MESH:D011225), pulmonary edema (MESH:D011654), bleeding (MESH:D006470), Obesity (MESH:D009765), arrhythmia (MESH:D001145), nausea (MESH:D009325), diastolic dysfunction (MESH:D018487), brain edema (MESH:D001929), NCDs (MESH:D000073296), Overweight (MESH:D050177), AKI (MESH:D058186), hypertensive retinopathy (MESH:D058437), stroke (MESH:D020521), PSH (MESH:D058246), vascular complications (MESH:D003925), kidney function decline (MESH:D007680), acute ischemic stroke (MESH:D000083242), proteinuria (MESH:D011507), acute aortic syndromes (MESH:D000208), convulsions (MESH:D012640), hypotension (MESH:D007022), stenosis (MESH:D003251), hypoxia (MESH:D000860), frailty (MESH:D000073496), hemolysis (MESH:D006461), LV mass reduction (MESH:C536030), damage (MESH:D020263), albuminuria (MESH:D000419), pulmonary congestion (MESH:D001261), salt and water retention (MESH:D016055), ASCVD (MESH:D050197), Renovascular hypertension (MESH:D006978), intracerebral hemorrhage (MESH:D002543), diastolic hypertension (MESH:C563897), death (MESH:D003643), white-coat hypertension (MESH:D059466), left ventricular hypertrophy (MESH:D017379), HBPM (MESH:D006973), hypertensive encephalopathy (MESH:D020343)
- **Chemicals:** sodium chloride (MESH:D012965), oxygen (MESH:D010100), chlorthalidone (MESH:D002752), salt (MESH:D012492), uric acid (MESH:D014527), aldosterone (MESH:D000450), Aspirin (MESH:D001241), DHP (MESH:C038806), Thiazide (MESH:D049971), cholesterol (MESH:D002784), ARNI (-), caffeine (MESH:D002110), sodium (MESH:D012964), potassium (MESH:D011188), atorvastatin (MESH:D000069059), magnesium sulfate (MESH:D008278), natriuretic peptides (MESH:D045265), carbohydrates (MESH:D002241), sacubitril (MESH:C000717211), Spironolactone (MESH:D013148), RA (MESH:D011883), labetalol (MESH:D007741), Lipid (MESH:D008055), alcohol (MESH:D000438), PM (MESH:D011399), indapamide (MESH:D007190), valsartan (MESH:D000068756), magnesium (MESH:D008274), glucose (MESH:D005947), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606], Actinopterygii (fishes, superclass) [taxon 7898]

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## References

245 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919385/full.md

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Source: https://tomesphere.com/paper/PMC12919385