Professional Documents
Culture Documents
Dyspepsia and Hypertension
Dyspepsia and Hypertension
Dyspepsia and Hypertension
Background: Dyspepsia is any chronic or recurrent discomfort in the epigastric area described as bloatedness, fullness,
gnawing or burning continuously or intermittently for at least 2 weeks. About 40% of the adult population may suffer
from dyspeptic symptoms but most of them are un-investigated because only about 2% consult their physician.
Method: The general objective of this clinical pathway is to improve outcomes of patients with dyspepsia in family and
community practice.
Method: The PAFP Clinical Pathways Group reviewed the previous Clinical Practice Guideline for the Treatment of Dyspepsia
in Family Practice, a local guideline developed by the Family Medicine Research Group and adopted as policy statement by the
Philippine Health Insurance Corporation. The reviewers then developed a time-related representation of recommendations on
patient care processes, in terms of history and physical examination, laboratory tests, pharmacologic and non-pharmacologic
interventions as well as social and community strategies to treat hypertension and prevent complications.
Recommendation: All patients with upper gastrointestinal pain or discomfort should have a detailed history focusing
on weight loss, hematemesis, hematochezia, melena, dysphagia, odynophagia, vomiting, NSAID intake, alcohol intake,
smoking, frequent medical complaints, depression, anxiety, personal or family history of gastrointestinal disease using
family genogram. Physical examination findings provide minimal information but should be done to rule out an organic
pathology and to look for alarm clinical features like anemia, abdominal tenderness or mass, jaundice, melena etc. If the
patient is with history of previous dyspepsia treatment, more than 45 years old or long-term use of NSAID, the physician
may request for non-invasive H. pylori test. Upper abdominal ultrasound, liver function test, pancreatic amylase may be
done if organic problem is considered. Start therapeutic trial of prokinetic treatment for 1-2 weeks or proton-pump inhibitor
depending on the symptoms. Fixed drug combination may be used if symptoms are undifferentiated. The patient should
be educated about upper gastrointestinal disorders and dyspepsia, risk factors and complications. If medications were
prescribed, explain the dose, frequency, intended effect, possible side effects and importance of medication adherence.
Lifestyle modifications focusing on low fat meals, weight reduction, avoidance of alcohol intake and smoking cessation,
eating way before bedtime, elevated head while sleeping, etc. may also be done. Recommendations were also made on
subsequent visits.
Implementation:
Quality improvement strategy is recommended for implementation of this pathway. This will involve pre- and post-intervention
data collection using records review. Intervention strategies may be feedback, group consensus or incentive mechanisms.
The PAFP QA Committee met as a panel and graded Evidence Grade Levels
the recommendations as shown in Table 1. The grading
system was a mix of the strength of the reviewed published I - The best evidence cited to support the recommendation
evidence and the consensus of a panel of experts. In some is a well-conducted randomized controlled trial. The
cases the published evidence may not be applicable if CONSORT standard may be used to evaluate a well-
Philippine family practice setting, so a panel grade based on conducted randomized controlled trial.
the consensus of clinical experts was also used. Thus if the
recommendation was based on a published evidence that II - The best evidence cited to support the recommendation
is a well done randomized controlled trial and the panel is a well-conducted observational study i.e. match
of expert voted unanimously for the recommendation, it control or before and after clinical trial, cohort studies,
was given a grade of A-I. If the level of evidence is based case control studies and cross-sectional studies. The
First Visit __All patients with upper __Request for non- Probably motility Patient interventions __Aware of initial
gastrointestinal pain or discomfort invasive H. pylori test if problem __Educate the patient about diagnosis (A-III)
should have a detailed history with history of previous __Start therapeutic upper gastrointestinal disorders __Aware of risk factors
focusing on weight loss, dyspepsia treatment, trial of prokinetic and dyspepsia, risk factors and and complications
hematemesis, hematochezia, more than 45 years old treatment for 1-2 complications (A-II) (A-III)
melena, dysphagia, odynophagia, or long-term use of weeks (A-I) __If medications were prescribed, __Aware of
vomiting, NSAID intake, alcohol NSAID (A-II) explain the dose, frequency, importance of
intake, smoking, frequent medical Probably acid- intended effect, possible side effects adherence to
complaints, depression, anxiety, __ Upper abdominal related problem and importance of medication diagnostics and
personal or family history of ultrasound, liver __Start therapeutic adherence (A-II) interventions (A-III)
gastrointestinal disease using family function test, trial with proton-pump __Lifestyle modifications focusing
genogram. (A-II) pancreatic amylase inhibitor or H2 blocker on low fat meals, weight reduction,
__ Physical examination findings if organic problem is for 1-2 weeks (A-I) avoidance of alcohol intake and
provide minimal information but considered (A-II) smoking cessation, eating way
should be done to rule out an Undifferentiated before bedtime, elevated head
organic pathology and to look for upper while sleeping, etc. (A-II)
alarm clinical features like anemia, gastrointestinal
abdominal tenderness or mass, problem Family interventions
jaundice, melena etc. (A-II) __Start therapeutic __Inquire and recommend family
trial with combination members’ lifestyle activities (A-III)
Pathway decisions of prokinetic and
__If there is organic/structural proton-pump inhibitor Community interventions
problem based on significant or H2 blocker for 1-2 __Inquire for community lifestyle
physical examination finding, refer weeks (A-I) activities (A-III)
to specific clinical pathway (A-III)
__Probably motility problem if Continuing Care
prominent history of bloatedness, __Follow-up after 1-2 weeks
dysphagia and vomiting (A-III) __Offer family wellness package
__Probable acid-related problem if (A-III)
prominent history of epigastric pain,
NSAID and alcohol intake and reflux
symptoms (A-III)
__Undifferentiated upper
gastrointestinal problem (A-III)
Variations
Second __Review and note any change __Request for Improved symptoms Patient interventions __Improved symptom
Visit in history focusing on weight loss, endoscopy if symptoms __Continue __Enhance education about control (A-I)
hematemesis, melena, dysphagia, did not improve with medications until 4 upper gastrointestinal disorders __Modification of
odynophagia, vomiting, NSAID therapeutic trial for 2-4 weeks (A-I) and dyspepsia, risk factors and risk factors i.e. diet,
intake, alcohol intake, smoking weeks (A-II) complications (A-II) lifestyle, smoking and
frequent medical complaints, With upper __If medications were prescribed, alcohol intake (A-I)
depression, anxiety, personal or __Complete request gastrointestinal enhance explanation on the dose, __Absence of new
family history of gastrointestinal for upper abdominal organic problem frequency, intended effect, possible complications (A-III)
disease using family genogram. ultrasound, liver __Refer to side effects and importance of __Adherence to
(A-II) function test and gastroenterologist or medication adherence (A-II) diagnostics and
__Repeat and note any change pancreatic amylase manage according __Enhance lifestyle modifications interventions (A-II)
in physical examination focusing if organic problem is to available clinical focusing on low fat meals, weight __Agreed plan for
on the upper gastrointestinal tract considered (A-II) pathway (A-III) reduction, avoidance of alcohol family intervention
(A-II) intake and smoking cessation, (A-III)
__Review the results of laboratory eating way before bedtime,
tests and response to empiric elevated head while sleeping, etc.
treatment (A-II) (A-II)
Family interventions
Pathway decisions __Enhance recommendation
__If there is symptom for family members’ appropriate
improvement with the therapeutic lifestyle activities (A-III)
trial, continue until 4 weeks (A-III)
__If no symptom improvement, Community interventions
refer for gastrointestinal endoscopy __Recommend participation in
(A-III) appropriate community lifestyle
__If the H pylori test is positive, activities like alcohol anonymous
start eradication treatment (A-III) (A-III)
__If ultrasound and other
laboratory tests are positive manage Continuing care
accordingly (A-III) __Follow-up after 1 month until
upper gastrointestinal symptom is
resolved and every 3-6 months if BP
target is already achieved (A-III)
Variations
Continuing __Review and note any change __Repeat request H Improved symptoms Patient interventions __Improved symptom
Visit in history focusing on weight loss, pylori test, endoscopy __Self-management __Enhance education about control (A-I)
hematemesis, melena, dysphagia, or upper abdominal with the same upper gastrointestinal disorders __Modification of
odynophagia, vomiting, NSAID ultrasound, liver medications for and dyspepsia, risk factors and risk factors i.e. diet,
intake, alcohol intake, smoking function test and symptom recurrence complications (A-II) lifestyle, smoking and
frequent medical complaints, pancreatic amylase if (A-I) __Educate the patient on alcohol intake (A-I)
depression, anxiety, personal or organic problem was self-management for symptom __Absence of new
family history of gastrointestinal considered after 3-6 With upper recurrence (A-II) complications (A-III)
disease using family genogram. months to monitor gastrointestinal __Enhance lifestyle modifications __Adherence to
(A-II) response to treatment organic problem focusing on low fat meals, weight diagnostics and
__Repeat and note any change (A-II) __Refer to reduction, avoidance of alcohol interventions (A-II)
in physical examination focusing gastroenterologist or intake and smoking cessation, __Implemented
on the upper gastrointestinal tract manage according eating way before bedtime, plan for family
(A-II) to available clinical elevated head while sleeping, etc. and community
__Review the results of endoscopy pathway (A-III) (A-II) intervention (A-III)
and other laboratory tests (A-II)
Family interventions
__Enhance recommendation
Pathway decisions for family members’ appropriate
__If endoscopy was positive for lifestyle activities (A-III)
bleeding peptic ulcer and other
serious organic problem consider Community interventions
transfer of care to gastroenterologist __Recommend participation in
(A-III) appropriate community lifestyle
__If there is continued positive activities like alcohol anonymous
response to therapeutic trial and (A-III)
H. pylori eradication continue with
current care (A-III) Continuing care
__Follow-up after 1 month until
upper gastrointestinal symptom
is resolved and every 6-12 months
(A-III)
Variations
Patients with dyspepsia will be consulting a physician’s • Dysmotility like dyspepsia - Agreus and Talley both
clinic for the following symptoms; recurrent epigastric pain, described this subgroup by naming the following most
heartburn or acid regurgitation, with or without bloating, bothersome symptoms: Upper abdominal discomfort
nausea or vomiting. These symptoms fit in the definition of (not pain); early satiety, bloating in upper abdomen,
dyspepsia adopted by the National Institute of Health Care post-prandial fullness, and nausea, retching or
and Clinical Excellence (NICE) in the United Kingdom.8 vomiting.12
The clinical history and physical examination must focus
on investigating for the presence of age at onset greater • Ulcer-like dyspepsia – Barbara’s article succinctly
than 45 years old, weight loss, anemia, hematemesis, described the symptoms as suggestive of peptic ulcer
melena, hematochezia, dysphagia, odynophagia, persistent diseases. Talley and Agreus agreed on the following
vomiting, abdominal mass, jaundice, chronic NSAID symptomatology: relapsing epigastric pain, aggravated
intake, chronic alcohol intake and previous history of by hunger and relieved by antacids.12
ulcer. These were considered alarm features in previous
guidelines and may signify that the patient may be at • Reflux-like dyspepsia – Talley and Agreus described
high risk. Other features like frequent medical complaints, the most bothersome symptom as heartburn and acid
depression, anxiety, family history of dyspepsia or peptic regurgitation which may awaken patient at night.12
ulcer disease and smoking should also be obtained.1 It
is also recommended to review medications for possible • Functional dyspepsia – Barbara briefly described this
causes of dyspepsia for example, calcium antagonists, subgroup as patients who report dyspeptic symptoms
nitrates, theophylline, bisphosphonates, corticosteroids in whom no disease can be identified by any clinical,
and nonsteroidal anti-inflammatory drugs (NSAIDs).8 biochemical, endoscopic, ultrasonographic pathology.
Gastrointestinal complaints are common among patients The diagnosis is usually made after an extensive
with somatization and anxiety disorders. A cohort study gastrointestinal diagnostic work-up.13
showed that certain personality characteristics like trait
anger reactivity and stress proneness, frequent use of Aside from the four symptom syndromes mentioned,
coping strategies and social stress predispose individuals family and community medicine practitioners may also
History and Physical Examination If the initial empiric treatment fails a trial of an
additional second drug may be done. H2 blocker therapy
Evaluate the patient’s response to empiric treatment. if there is an inadequate response to a PPI may be added.8
If laboratory evaluation was requested, evaluate the Cure of H. pylori infection decreases recurrence rates and
results. Review the history and physical examination facilitates healing. Thus antibiotic therapy is indicated for
and correlate with results of laboratory and response to all H. pylori-infected patients. No optimal, simple antibiotic
empiric treatment. Consider referral to a specialist service regimen has yet emerged.
for patients of any age with gastro-oesophageal symptoms While choosing a treatment regimen for H. pylori,
that are non-responsive to treatment.8 patients should be asked about previous antibiotic
exposure and this information should be incorporated
Laboratory Tests into the decision-making process. For first-line treatment,
clarithromycin triple therapy should be confined to patients
If empiric treatment or after a trial of a second drug with no previous history of macrolide exposure who reside
fails, then further investigation should be considered. Upper in areas where clarithromycin resistance amongst H. pylori
gastrointestinal endoscopy and H pylori testing are valuable isolates is known to be low. Most patients will be better
diagnostic tools that can guide future clinical decisions. The served by first-line treatment with bismuth quadruple
need for endoscopy is a difficult decision in patients with therapy or concomitant therapy consisting of a PPI,
dyspepsia. It is costly and not readily available in family and clarithromycin, amoxicillin, and metronidazole.30
community practice. However early endoscopy will often The Asia-Pacific Consensus Conference recommended
prove more cost effective than delaying until the indications H. pylori eradication among infected patients with
are clearer.29 functional dyspepsia and those receiving long-term
H. pylori testing is another test to be considered. There maintenance proton pump inhibitor for gastroesophageal
is now direct clinical evidence supporting a test-and-treat reflux disease. In Asia, the currently recommended first-
approach in patients with dyspepsia symptoms.22 Empiric line therapy for H. pylori infection is PPI-based triple
H. pylori eradication therapy is not recommended. therapy with amoxicillin/metronidazole and clarithromycin
The role of H. pylori is an important development in for 7 days, while bismuth-based quadruple therapy is an
gastroduodenal disease. It has changed our understanding effective alternative. There appears to be an increasing
of the pathophysiology of diseases in the in the upper rate of resistance to clarithromycin and metronidazole in
gastrointestinal tract. It may also have a role in un- parts of Asia, leading to reduced efficacy of PPI-based triple
investigated and functional dyspepsia and ulcer risk in therapy.34 The recommended doses are a twice daily, seven-
patients taking low-dose aspirin or starting therapy with a day regimen of a proton pump inhibitor (omeprazole 20
non-steroidal anti-inflammatory medication.30 Eradication mg, lansoprazole 30 mg, pantoprazole 40 mg) or ranitidine
of the bacterium resulted to faster cure of peptic ulcer disease bismuth citrate 400 mg, plus clarithromycin 500 mg and
and decreased the symptoms of non-ulcer dyspepsia.31 amoxicillin 1000 mg, or plus clarithromycin 500 or 250
H. pylori infection can be accurately diagnosed with urea mg and metronidazole 500 mg.35,36 This usually result to
breath test or a stool antigen test. It can also be diagnosed eradication of H. pylori infection in 80-90% of cases. In case
invasively by histology or culture.32 Proton pump inhibitor of lack of efficacy, the 7-14 day treatment may be repeated
therapy should be stopped at least 1 week prior to H pylori using triple therapies (PPI + 2 antibiotics) substituting
testing.33 the antibiotic with the metronidazole or tetracycline, or
Noel L. Espallardo, MD, MSc, FPAFP; Limuel Anthony B. Abrogena, MD, FPAFP; Marishiel Mejia-Samonte, MD, DFM
Anna Guia O. Limpoco, MD, FPAFP and Ryan Jeanne V. Ceralvo, MD, FPAFP
Background: Hypertension is a major risk factor for cardiovascular disease. The prevalence of hypertension in the Western
Pacific Region is 37% of adults older than 24, while in the Philippines it is 25% of adults 21 years old and above. Several
guidelines have been developed for the management of hypertension. All these guidelines have recommendations for
assessment and treatment.
Objectives: The overall objective of the development and implementation of this clinical pathway is to improve outcomes
of patients with hypertension seen in family and community practice.
Methods: The PAFP Clinical Pathways Group reviewed published medical literature to identify, summarize, and operationalize
the clinical content of diagnostics, interventions and clinical indicators or outcomes to develop an evidence-based clinical
pathway in family medicine practice. The group developed a time-related representation of recommendations on patient
care processes, in terms of history and physical examination, laboratory tests, pharmacologic and non-pharmacologic
interventions as well as social and community strategies to treat hypertension and prevent complications.
Recommendations: Recommendations were made based on the number of visits. During the first visit, all adult patients
consulting at the clinic should be screened for hypertension with appropriate BP measurement. A thorough history
focusing on symptoms, family history using genogram, smoking and other lifestyle and co-existing chronic disease and
a thorough physical examination focusing on the weight/BMI, waist/hip ratio, funduscopy, neurological, cardiac, renal
and peripheral arteries should be done. For the laboratory, request for 12-lead ECG, urinalysis, FBS, creatinine, serum K
and lipid profile to determine co-morbidities and baseline values. If the patient is already diagnosed hypertensive, start/
continue medications with either or a combination of thiazide-type diuretic, calcium channel blockers, angiotensin-
converting enzyme inhibitors and angiotensin receptor blocker depending on co-morbidities or side effects. But if there
is a need for further confirmation, no medication is warranted. Educate the patient about hypertension, risk factors and
complications. If medications were prescribed, explain the dose, frequency, intended effect, possible side effects and
importance of medication adherence. Lifestyle modifications focusing on weight control, exercise and smoking cessation
should be adviced. During the first visit it is expected that the patient is aware of the diagnosis of hypertension, its risks
factors and complications to encourage compliance.
Implementation: Education, training and audit are recommended strategies to implement the clinical pathway.
Table 1. Grading of the recommendations. In the implementation of the clinical pathways, the
PAFP QA committee strongly recommend compliance
Panel Grade Level Evidence Grade Level to guideline recommendations that are graded as
1 2 3
either A-I, A-II or B-I. However, the committee also
A A-I A-II A-III recommend using sound clinical judgment and patient
B B-I B-II B-III involvement in the decision making before applying the
C C-I C-II C-III recommendations.
First Visit __All adult patients consulting Diagnosed Diagnosed Patient interventions __Aware of initial
at the clinic should be screened hypertension hypertension __Educate the patient about diagnosis (A-III)
for high blood pressure with __Request for 12- __Start/continue hypertension, risk factors and __Aware of risk factors
appropriate BP measurement (A-III) lead ECG, urinalysis, medications with complications (A-I) and complications
__Make a thorough history FBS, creatinine, either or a combination __If medications were prescribed, (A-III)
focusing on symptoms, family serum K and lipid of thiazide-type explain the dose, frequency, __Aware of
history using genogram, smoking profile to determine diuretic, calcium intended effect, possible side effects importance of
and other lifestyle and co-existing co-morbidities and channel blockers, and importance of medication adherence to
chronic disease (A-II) baseline values (B-II) angiotensin-converting adherence (A-I) diagnostics and
__Make thorough physical enzyme inhibitors and __Lifestyle modifications focusing interventions (A-III)
examination focusing on the Pathway decisions angiotensin receptor on weight control, exercise and
weight/BMI, waist/hip ratio, __ For patients with blocker depending on smoking cessation (A-I)
funduscopy, neurological, cardiac, previously diagnosed co-morbidities or side
renal and peripheral arteries (A-II) co-morbidities, refer effects (A-I) Family interventions
to specific pathway __Inquire and recommend family
Pathway decisions for management of Need to confirm members’ lifestyle activities (A-I)
__If BP is ≥ 140/90 mmHg with co-morbidity (A-III) hypertension
signs and symptoms of acute end- __No medications are Community interventions
organ damage, consider referral to warranted (A-III) __Inquire for community lifestyle
hospital (A-III) activities (A-III)
__If the initial BP is ≥ 180/110 Patients for
mmHg consider hypertension and emergency referral Continuing care
start medication. (A-III) __Consider giving a __Follow-up after 1-2 weeks (A-II)
__IF BP is ≥ 140/90 mmHg single dose of anti- __Offer family wellness package
and with previous history of hypertensive prior to (A-III)
high BP taken by another health transport (A-I)
professional within the month
consider hypertension and start
medication. (A-III)
__If BP is ≥ 140/90 mmHg and first
time high BP confirm with home
BP measurements or second visit
within 4 weeks (A-III)
Variations
Second __Review and note any change Diagnosed Diagnosed Patient interventions __Improved BP control
Visit in history focusing on symptoms, hypertension hypertension __Enhance education about (Age 18 to 59: <140/90
family history using the genogram, __Complete request __Start/continue hypertension, risk factors and mmHg;
smoking and other lifestyle and co- for 12-lead ECG, medications with complications (A-I) Age > 60: <150/90
existing chronic disease (A-II) urinalysis, FBS, either or a combination __If medications were prescribed, mmHg) (A-II)
__Repeat and note any change in creatinine, serum of thiazide-type repeat explanation about the dose, __ Body mass index
physical examination focusing on K and lipid profile diuretic, calcium frequency, intended effect, possible between 18.5-24.9 kg/
the weight/BMI, waist/hip ratio, to determine channel blockers, side effects and importance of m2 (A-II)
funduscopy, neurological, cardiac, co-morbidities and angiotensin-converting medication adherence (A-I) __Modification of
renal and peripheral arteries (A-II) baseline values (B-II) enzyme inhibitors and __Enhance advice on lifestyle risk factors i.e. diet,
__Review BP monitoring if angiotensin receptor modifications focusing on weight lifestyle, smoking and
available (A-II) blocker depending on control, exercise and smoking exercise (A-II)
__Review laboratory results and Pathway decisions co-morbidities or side cessation (A-I) __Absence of new
establish the presence of other risk __ For patients with effects (A-I) complications (A-III)
factors and co-morbidities (A-II) previously diagnosed Family interventions __Adherence to
co-morbidities, refer With co-morbidities __Enhance recommendation diagnostics and
to specific pathway __Refer to clinical for family members’ appropriate interventions (A-II)
Pathway decisions for management of pathway of the co- lifestyle activities (A-I) __Agreed plan for
__If home BP and/or second visit co-morbidity (A-III) morbidity (A-III) family intervention
BP are ≥ 140/90 mmHg diagnose as Community interventions (A-III)
hypertension (A-II) __Recommend participation in __Agreed plan
__If home BP and/or second visit appropriate community lifestyle for community
BP are < 140/90 mmHg rule out activities (A-III) involvement (A-III)
hypertension but monitor after 6-12
months (A-III) Continuing care
__Follow-up after 1 month until
BP target is achieved and every
3-6 months if BP target is already
achieved (A-III)
Variations
Continuing __Review and note any change Diagnosed Diagnosed Patient interventions __Improved BP control
Visit in history focusing on symptoms, hypertension hypertension __Enhance education about (Age 18 to 59: <140/90
family history using genogram, __After 6-12 months __Continue/revise hypertension, risk factors and mmHg;
smoking and other lifestyle and co- repeat for 12-lead medications with complications (A-I) Age > 60: <150/90
existing chronic disease (A-II) ECG, urinalysis, FBS, either or a combination __If medications were prescribed, mmHg) (A-II)
__Repeat and note any change in creatinine, serum K and of thiazide-type repeat explanation about the dose, __ Body mass index
physical examination focusing on lipid profile (B-II) diuretic, calcium frequency, intended effect, possible between 18.5-24.9 kg/
the weight/BMI, waist/hip ratio, channel blockers, side effects and importance of m2 (A-II)
funduscopy, neurological, cardiac, angiotensin-converting medication adherence (A-I) __Modification of
renal and peripheral arteries (A-II) Pathway decisions enzyme inhibitors and __Enhance advice on lifestyle risk factors i.e. diet,
__Review laboratory results and __ For patients with angiotensin receptor modifications focusing on weight lifestyle, smoking and
establish the presence of other risk previously diagnosed blocker depending on control, exercise and smoking exercise (A-II)
factors and co-morbidities (A-II) co-morbidities, refer co-morbidities or side cessation (A-I) __Absence of new
to specific pathway effects (A-I) complications (A-III)
Pathway decisions for management of Family interventions __Adherence to
__Enhance/revise pharmacologic co-morbidity (A-III) With co-morbidities __Enhance recommendation diagnostics and
and non-pharmacologic __Refer to clinical for family members’ appropriate interventions (A-II)
interventions until BP control is pathway of the co- lifestyle activities (A-I) __Agreed plan for
achieved (Age 18 to 59: <140/90 morbidity (A-III) family intervention
mmHg; Community interventions (A-III)
Age > 60: <150/90 mmHg) (A-III) __Recommend participation in __Agreed plan
appropriate community lifestyle for community
activities (A-III) involvement (A-III)
Continuing care
__Follow-up after 1 month until
BP target is achieved then every
3-6 months if BP target is already
achieved (A-III)
Variations
Irbesartan* 150 and 300 mg tab Diabetics and mild Fatigue, edema, nausea, Contraindicated in moderate
150 – 300 mg per day renal disease vomiting, dizziness, headache to severe renal impairment,
OD pregnancy and lactation
Losartan*+ 50 and 100 mg tab LVH and for renal Diarrhea, abdominal Contraindicated in pregnancy
50 – 100 mg per day protection in Type 2 pain, nausea, headache, and co-administration with
OD diabetic patients dizziness, hyperkalemia, aliskiren in diabetic patients
hypotension, URI symptoms,
angioedema, anemia, liver
function abnormalities,
vomiting, myalgia, arthralgia,
photosensitivity
Valsartan* 80, 160 and 320 mg tab Heart failure, post-MI, Dizziness, postural dizziness, Contraindicated in pregnancy
80 – 320 mg per day delay of diabetes hypotension, renal failure and
OD for maintenance progression in impairment
BID for HF and MI hypertensives at CV risk
°40 mg per day for and children 6 – 18 y/o
children <35 kg
Cardioselective Beta-blockers (BBs)
Atenolol* 25, 50 and 100 mg Angina, MI or heart Bradycardia, decreased libido Contraindicated in sinus
tablet failure bradycardia, cardiogenic shock,
25 – 100 mg per day acute unstable HF
OD
Metoprolol* 50 and 100 mg tablet Angina, MI or heart Fatigue, weakness, orthostatic Contraindicated in sinus
100 – 400 mg per day failure hypotension, impotence, bradycardia, cardiogenic shock,
BID drowsiness, bradycardia, acute unstable HF
pulmonary edema, CHF
Propranolol 10 and 40 mg tab Angina, anxiety, Fatigue, weakness, orthostatic Take before meals
160-320 mg per day migraine, post-MI, hypotension, impotence, Contraindicated in patients with
BID arrhythmia drowsiness, bradycardia, history of bronchial asthma
pulmonary edema, CHF or bronchospasm, cardiogenic
shock, tachycardia, 2nd and 3rd
degree block
Calcium Channel Blockers (CCBs)
Nifedipine 5, 30 mg cap Headache, vomiting 5 mg preparation is short-acting
5-30 mg per day 30 mg preparation is extended-
release
Felodipine* 2.5, 5 and 10 mg tab Peripheral edema, headache, Contraindicated for unstable
2.5 – 10 mg per day flushing, palpitations angina, uncompensated heart
OD failure, acute MI, pregnancy
Combined Alpha & Beta Blocker
Carvedilol* 6.25 and 25 mg tab Angina and mild to Diarrhea, nausea, dizziness, Contraindicated in unstable
6.25 – 50 mg per day moderate heart failure abnormal or blurred vision heart failure, 2nd or 3rd degree
OD - BID AV block, severe bradycardia or
hypotension, history of COPD or
bronchospasm
Thiazide Diuretics
Hydrochlorothiazide 12.5 and 25 mg tab Edema and Dry mouth, thirst, weakness, Contraindicated in renal
12.5 - 100 mg per day nephrogenic diabetes lethargy, muscle pain, cramps, impairment, can cause
OD insipidus hypotension hyperglycemia
Combination drugs
Hydrochlorothiazide- Hydrochlorothizide Dry mouth, thirst, weakness, Contraindicated in renal
losartan (50-100mg)-losartan lethargy, muscle pain, impairment, can cause
(12.5-25mg) cramps, hypotension diarrhea, hyperglycemia, pregnancy
abdominal pain, nausea,
headache, dizziness, URI
symptoms, cough
Goals Recommendations
Lifestyle Encourage family meals adhering to DASH eating plan, wherein food served should be
Family Diet HIGH in: Fruits and vegetables (4-5 servings each per day; fiber (7-8 servings per day); low fat dairy products (2-3 servings per day); lean
meat (2 servings per day); calcium; magnesium; potassium
LOW in saturated fat, cholesterol, salt such as unsalted nuts, almonds, peanuts, chocolate, cocoa butter, coconut
Increase intake of polyunsaturated fatty acids such as *Foods and oils including walnuts, sunflower seeds, fish such as salmon, mackerel,
corn oil, soybean oil
Goals Recommendations
Lifestyle Inquire if patient and family aware of existing community lifestyle activities
Family Diet
Community Programs Inquire if patient and family aware and willing to participate in existing local health center and programs on hypertension in the
community
During the second and continuing visits, repeated During the second visit, the patient should have
delivery of educational intervention should be done. During increased awareness about the diagnosis and potential risks
the first and second visits face-to-face, paper-based or associated with hypertension. As a result of this awareness,
digital method of health education should be done. But adherence to interventions should be achieved. Adherence
when opportunity arise, behavioral intervention such as can be achieved by repeating/enhancing the interventions
counselling may be done later. The use of patient diaries done during the earlier visits.
may be helpful to monitor adherence. Adherence to intervention may be a surrogate outcome
With regards to exercise, once the patient is used to leading to successful management of hypertension. One
rhythmic lower limb exercise, the patient may move up to study evaluated the effect of adherence on cardiovascular
moderate to vigorous aerobic (endurance) activity up to disease mortality, cerebral hemorrhage and cerebral
5 days/week. Resistance training (strength) on 2 or more infarction. Adherence were classified into good (cumulative
non-consecutive days/week. Vigorous exercise training medication adherence, ≥80%), intermediate (cumulative
is generally safe and well tolerated by most people, medication adherence, 50%-80%), and poor (cumulative
including those with hypertension, although some special medication adherence, <50%) adherence groups. The
considerations are required for safety.28 results showed that patients with poor medication
The effectiveness of educational and organizational adherence had worse mortality from ischemic heart disease
strategies used to improve control of blood pressure was (hazard ratio, 1.64; 95% confidence interval, 1.16-2.31;
examined in a systematic review of randomized controlled P for trend=0.005), cerebral hemorrhage (hazard ratio, 2.19;
trials. The following interventions were evaluated: self- 95% confidence interval, 1.28-3.77; P for trend=0.004),
monitoring and educational interventions directed to the and cerebral infarction (hazard ratio, 1.92; 95% confidence
patient. The results showed that a system of regular review interval, 1.25-2.96; P for trend=0.003) than those with
and self-monitoring of antihypertensive drug therapy was good adherence. Similar findings were also noted with
shown to reduce blood pressure and all-cause mortality at hazard ratio for hospitalization.30
5 years follow-up. Antihypertensive drug therapy should be For those already prescribed with medications, the
monitored closely and adopt a stepped care approach when goal should be a blood pressure lower than the baseline.
patients do not reach target blood pressure levels.29 Based on guideline recommendations the goal differ among
patients above or below 60 years old. For patients less than
Reinforce BP goals, self-monitoring and recording Encourage family members to adhere to healthy Encourage family members to join programs on
lifestyle hypertension in the community
Reinforce compliance to antihypertensives Compliance to healthy family meals Enrolment in existing community lifestyle activities
Reinforce adherence to lifestyle modification Adherence to family fitness activities Actively participating in hypertension support
(targeted weight, diet and fitness) groups in the community