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Status unknownNCT03630380Updated Sep 18, 2019

Accuracy of Clinical and Diagnostic Studies for Pneumonia in Children

An observational study in Pneumonia, sponsored by Patan Academy of Health Sciences. Status unknown at 1 site in Nepal. Open to participants aged Up to 59 Months. Per ClinicalTrials.gov, last updated 2019-09-18.

Sponsored by Patan Academy of Health Sciences · Observational

The sponsor has not verified this record recently (last verified Sep 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
1,000
Ages
Up to 59 Months
Sex
All
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Study summary

Pneumonia continues to be a leading cause of death in children under five years of age worldwide. Many studies have evaluated clinical signs and symptoms that may predict pneumonia. A recent meta-analysis found that no singular physical exam finding predicted pneumonia. The World Health Organization (WHO) Criteria diagnose pneumonia based on fast breathing; however, tachypnea has not been shown to strongly predict pneumonia. This study will evaluate accuracy of clinical history, physical exam and WHO criteria, laboratory findings, and lung ultrasound compared with chest radiograph for the diagnosis of pneumonia in children under five years of age in a resource limited setting. Determining diagnostic accuracy of these findings may help derive a clinical decision rule that may more accurately predict which children have pneumonia than current WHO guidelines.

Read the detailed description

Background Pneumonia is the leading cause of death in children under five years of age worldwide.1 These deaths may be prevented by early detection and targeted antibiotic therapy.2 However, the diagnosis is not always clear on presentation to health care facilities. Missed diagnosis may lead to increased morbidity and mortality, while over-diagnosis may lead to unnecessary antibiotic use, which may further lead to increased antibiotic resistance, cause allergic reactions, and create unnecessary costs for patients. Therefore, using clinical tools and diagnostic capabilities to better improve diagnosis is critical.

Many studies have evaluated clinical signs and symptoms that may predict pneumonia.3-6 A recent meta-analysis found that no singular physical exam finding predicted pneumonia.5 The World Health Organization (WHO) Criteria diagnose pneumonia based on fast breathing; however, tachypnea has not been shown to strongly predict pneumonia.7 Additionally, most children with fever have compensatory tachypnea as a result, making the criteria of fast breathing difficult to diagnose pneumonia alone.8 In Nepal, one study evaluating the WHO criteria for pneumonia found a sensitivity of only 69.6% and specificity of 59.6%.9 Despite this, many providers rely on clinical exam findings and the WHO criteria for diagnosing pneumonia.

When available, diagnostic imaging is used regularly to confirm suspected pneumonia. Chest x-ray has been the standard for diagnosis in most facilities worldwide. However, remote facilities in resource-limited settings often lack radiographic imaging capabilities. Many facilities have bedside ultrasound available as it is easily portable, repeatable, and not associated with radiation. Ultrasound has been shown to be sensitive and specific for the diagnosis of pneumonia, yet few studies have evaluated the accuracy of lung ultrasound for pneumonia in pediatric patients in a resource-limited setting.10-14

The objective of this study is to evaluate the diagnostic accuracy of clinical history, physical exam, laboratory findings, and lung ultrasound compared to chest x-ray for the diagnosis of pneumonia in pediatric patients in a resource-limited setting. Determining diagnostic accuracy of these findings may help derive a clinical decision rule that may more accurately predict which children have pneumonia than current WHO guidelines.

Study Design

A prospective observational cross-sectional study of pediatric patients presenting for fever or respiratory complaints to the emergency department and outpatient department at Patan Hospital in Lalitpur, Nepal will be done over one year. Ethical approval will be obtained from the Nepal Health Research Council Ethical Review Board.

Study Setting and Population

Located in the Kathmandu valley, Patan Hospital is a large urban hospital with a 35-bed emergency department. The emergency department has an annual volume of approximately 48,000 patients, including approximately 8,000 pediatric visits. The admission rate is 20%.

Inclusion Criteria: Patients presenting under age 5 years of age with fever, respiratory complaints, or concern for pneumonia and receiving chest x-ray imaging.

Study Protocol

Parents will be consented for inclusion of child in the study (See consent form). Data will be collected on pediatric patients meeting the above inclusion criteria. Data will include demographics (age, gender), duration of symptoms, symptoms (presence or absence of fever, cough, chest pain, difficulty breathing, or vomiting), vital signs (temperature, respiratory rate, oxygen saturation), other physical exam findings (grunting, nasal flaring, retractions or indrawing of chest, crepitations, wheezing, or diminished breath sounds). These will be collected on the data collection form (see Appendix 1). Additionally, white cell counts with neutrophil counts and c-reactive protein will be collected if ordered by the clinician.

As a part of the evaluation, a bedside lung ultrasound will be performed by a clinician trained to perform lung ultrasounds. The bedside lung ultrasound is provided free for patients. Sonographers will be blinded to clinical information and results of any chest imaging. A Sonosite M Turbo (Fujifilm Sonosite, Inc.) ultrasound machine with a curvilinear probe will be used. In accordance with previous literature, the ultrasound examination will include ten views: two anterior views and two lateral views (one including the costophrenic angle), and one posterior view on each hemithorax. The physician will record ultrasound findings and interpretation directly after the ultrasound is complete. An ultrasound diagnosis of pneumonia is defined as the presence of unilateral B lines or subpleural lung consolidation. All ultrasounds will be reviewed for accuracy by a medical sonographer.

All patients will have a single posterioranterior (PA) chest x-ray as a part of the standard evaluation. The chest x-ray will be read by a board-certified radiologist, who is blinded to the clinical presentation and the results of any other imaging. Chest x-ray readings will be recorded on the standardized data form.

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Conditions studied

  • Pneumonia

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03

In context

Pneumonia

1,564 studies on the registry are indexed under Pneumonia; 265 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 252 across 535 observational studies indexed under Pneumonia.

Browse Pneumonia studies →

Lead sponsor

Patan Academy of Health Sciences is the lead sponsor of 7 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Up to 59 Months
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Located in the Kathmandu valley, Patan Hospital is a large urban hospital with a 35-bed emergency department. The emergency department has an annual volume of approximately 48,000 patients, including approximately 8,000 pediatric visits. The admission rate is 20%.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients presenting under age 5 years
  • Presence of fever, respiratory complaints, or concern for pneumonia
  • Receiving chest x-ray imaging

Exclusion criteria

Exclusion Criteria:

  • Children not receiving chest x-ray imaging as part of their workup for possible pneumonia
  • Patients 5 years of age and older
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
1,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Single Arm

    All children under five years of age with clinical suspicion of pneumonia (fever or respiratory complaints) who have a chest radiograph ordered will be consented. Clinical history, physical exam findings (temperature, respiratory rate, oxygen saturation, and lung auscultation findings), laboratory findings (white blood cell count, differential, and CRP) will be recorded. Lung ultrasound will be performed on all patients.

    Other: Clinical History · Other: Physical Exam Findings · Other: Laboratory Findings · Other: Lung Ultrasound

Interventions

  • OtherClinical History

    We will collect clinical history for each patient (days of illness, history of fever, cough, difficulty breathing, vomiting, chest pain).

  • OtherPhysical Exam Findings

    We will collect physical exam findings including vital signs, WHO criteria for diagnosing pneumonia, and lung auscultation findings.

  • OtherLaboratory Findings

    We will collect laboratory findings (white blood cell counts, differential, and c-reactive protein) if ordered by the clinician.

  • OtherLung Ultrasound

    We will perform lung ultrasound on all patients.

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What researchers measure

Primary outcomes

  1. Sensitivity

    We will follow patients during their acute visit to evaluate accuracy of clinical history, physical exam findings (including WHO criteria for diagnosing pneumonia), laboratory findings, and lung ultrasound using chest radiographs as the standard for diagnosing pneumonia. We will determine the sensitivity and specificity, and area under the receiver operator curve and determine if there are better combination of clinical and diagnostic predictors for diagnosis of pneumonia in children.

    Time frame: 1 day

  2. Specificity

    We will follow patients during their acute visit to evaluate accuracy of clinical history, physical exam findings (including WHO criteria for diagnosing pneumonia), laboratory findings, and lung ultrasound using chest radiographs as the standard for diagnosing pneumonia. We will determine the sensitivity and specificity, and area under the receiver operator curve and determine if there are better combination of clinical and diagnostic predictors for diagnosis of pneumonia in children.

    Time frame: 1 day

  3. Area under the receiver operator curve (ROC)

    We will follow patients during their acute visit to evaluate accuracy of clinical history, physical exam findings (including WHO criteria for diagnosing pneumonia), laboratory findings, and lung ultrasound using chest radiographs as the standard for diagnosing pneumonia. We will determine the sensitivity and specificity, and area under the receiver operator curve and determine if there are better combination of clinical and diagnostic predictors for diagnosis of pneumonia in children.

    Time frame: 1 day

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Study locations

1 of 1 sites recruiting
  • Patan Academy of Health Sciences
    Kathmandu, Nepal
    Recruiting
    • Yogendra Amatya, MDGP · Contact
    • Yogendra Amatya, MD GP · Principal investigator
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References and documents

Individual participant data

Plan to share: Undecided — The individual participant data will likely be placed on a data repository site.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03630380
Lead sponsor
Patan Academy of Health Sciences
Responsible party
Darlene Rose House (Assistant Professor of Clinical Emergency Medicine, Patan Academy of Health Sciences) — Principal investigator
First posted
Aug 14, 2018
Start date
Jun 1, 2018
Primary completion
May 31, 2020 (estimated)
Completion
Jul 31, 2020 (estimated)
Last update
Sep 18, 2019

Study contacts

Darlene R House, MD
Contact
drhouse@hotmail.com
9810339799
Darlene R House, MD
principal investigator · Patan Academy of Health Sciences

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Sep 2019. You cannot join it, but the record below documents what was studied.

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