Circ2022 0028
Circ2022 0028
PHILHEALTH CIRCULAR
No. ::J- 0 d- ';)-.. - 0 0 ;)._ 15
I. RATIONALE
Republic Act no. 11223 otherwise known as the Universal Health Care Act, provides that the
Corporation shall support the implementation of standards for clinical care set forth by the
Department of Health (DOH) based on approved clinical practice guidelines. Further, Section
51 of the revised Implementing Rules and Regulations of the National Health Insurance Act of
2013 (RA7875 as amended by RA9241 and RA10606) provides the implementation of quality
assurance standards as reference for ensuring quality of health care services.
When the WHO declared coronavirus disease 2019 (COVID-19) a global pandemic on March
2020, providing quality and safe care to patients proved to be challenging in many health care
systems including the Philippines. The diagnosis and treatment recommendations were based on
early scientific evidence that is rapidly evolving. Despite it, there is a need to come-up with
recommendations based on best available evidence that need to be carefully balanced with clinical
judgement.
The released interim guidelines by the World Health Organization (WHO) and the Philippine
Society of Microbiology and Infectious Diseases (PSMID) were used as references in the
development of policy statements. Further, consultative activities with the Philippine College of
Physicians (PCP) and PSMID were conducted during the development stages. Furthermore, the
Phi!Health Quality Assurance Committee (QAC) has approved it as reference in ensuring quality
of care, educational resource, performance monitoring, among others.
OBJECTIVES
B. Define the presence of risk and/ or co-morbidities of the patient to indicate hospital
admissibility, which is essential in claims for mild pneumonia.
III. SCOPE
A This Phi!Health Circular shall serve as reference for all accredited health care providers
B. This policy shall be applicable for adult patients who are hospitalized for respiratory illness
due to SARS CoV-2.
A. Coronavirus - a large family of viruses causing a range of illness in people from the common
colds to more infection that is serious and a variety of disease in farm animals and
domesticated pets.
V. POLICY STATEMENTS
A. Clinical Presentation
a. Flu-like symptoms such as dry cough, rhinonhea (nasal congestion), sore throat,
dyspnea, body malaise, fatigue (muscle soreness), and with/ out fever.
b.l. Anosmia (loss of smell) and/ or dysgeusia (loss of taste) precede respiratory
symptoms
b.2. Shortness of breath
bJ. Headache
b.4. Rhinorrhea (nasal congestion)
b.S. Myalgia
b.6. Diarrhea
b.7. Nausea and vomiting
2. High-risk adults and/ or having underlying health conditions are known to have co-
morbidity(-ies) increases the risk for poor outcome, which may include, but are not limited,
to the following:
2. Repeat testing for patients with an initial negative COVID-19 test result should be
performed ONLY if there is a high index of suspicion for COVID-19 infection despite an
initial negative test result.
3. If two RT-PCR tests yield negative results and patient may have symptoms for at least 15
days that are highly suggestive of COVID-19, an antibody test may be performed as a
confirmatory test.
4. For RT-PCR test to be valid should be taken within 2 weeks (14 days) from the onset of
!mown symptoms related to SARS-CoV2 infection.
C. Chest Imaging
The diagnosis of respiratory illness due to COVID-19 can be made on clinical grounds but
the following chest imaging modalities may assist in the diagnosis and identification or
exclu~ion of pulmonary complications:
2. Chest x-ray may appear normal initially, especially in mild cases. The common finding in
chest radiograph is the presence of infiltrates, which is usually bilateral than unilateral.
Other descriptive findings include hazy opacities, often rounded in morphology, with
peripheral and lower lung distribution, consolidation and pleural effusion.
I 3. Chest CT scan can detect early pneumonia before symptom onset and show ground glass
opacities in the lungs typically bilateral, but may be unilateral. Other findings include
\ peripheral distribution of fine reticular opacities and vascular thickenings.
The recommended diagnostic tests are, but not limited to the following when COVID-19 is
suspected/ probable/ confirmed to guide management, depending on the patient's
presentation and/ or service capability of the health facility: (refer to PSMID Guideline,
Summary of Diagnostic Tests for additionaV detailed information on guidance of use).
a. Without pneumonia
a.l. with risk factors for progression elderly (60 years old and above)
a.2. and/ or with co morbidities
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3. Severe COVID-19 case
b. Requires supplemental oxygen therapy with regular assessment for need of intubation
and mechanical ventilation.
c. Patients are closely monitored for signs of clinical deterioration, such as rapidly
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4. Critica!COVID-19 case
a. Critical pneumonia is a severe form associated with any of the following conditions:
b. Severely hypoxemic patients should be monitored closely in an ICU setting/ set-up for
clinical deterioration and progression to ARDS and need for invasive mechanical
ventilation is considered.
c. For patients who refuse intubation or with advance directives should be properly
documented in the patient chart by the attending physician or any authorized physician.
F. Management
c. Regular assessment of blood oxygenation to determine the need for intubation and
mechanical ventilation.
5. There is insufficient evidence to support the use of intravenous immunoglobulin (IV Ig)
for the management of COVID-19 among moderate/ severe hospitalized patients
EXCEPT in the context of a clinical trial.
6. There is insufficient evidence to support the routine use of interferon (IFN) for
patients hospitalized with COVID-19 EXCEPT in the context of a clinical trial or for
compassionate use.
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8. The recommendations on the use of investigational drugs are mainly based on research
outcomes and safety data. It should be discussed with the patient or a legally authorized
representative carefully outlining the potential adverse reactions and the potential clinical
benefits of these investigational drugs. A signed informed consent should be obtained by
the clinician. For reimbursement, investigational drugs shall be subjected to current
applicable benefit policy.
G. Hospital Discharge
2. Patients who have clinically recovered (with resolution of symptoms) may be discharged
from the hospital at the discretion of the healthcare team.
1. The health care provider shall be bound by the proviSions of the Performance
O.nnmitment and subject to the rules on monitoring and evaluation of performance as
provided in PhllHealth Orcular No. 2018-0019 Health Care Provider Performance
Assessment System (HCP-PAS) rev.2.
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II. DATE OF EFFECTIVITY
This PhllHealth Orcular shall take effect fifteen (15) days after publication in the Official Gazette
or in any newspaper of general circulation. A copy shall thereafter be deposited to the Office of
(j the National Administrative Register (ONAR) at the University of the Philippines Law Center.
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EMMANUEL R. LEDESMA, JR.
Acting President and Chief Executive Officer
t/
Date signed: -I'L' -/ 1- -'l-1..
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Oualit_y Policy on the Diagnosis and Management of COVID-19 (In-Patient) in Adult as Refetence of the
Corporation
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