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Radiological Characterization of Pulmonary Involvement in Patients With Hematological Diseases

N

New Valley University

Status

Enrolling

Conditions

Hematologic Diseases

Treatments

Diagnostic Test: Lactate dehydrogenase
Diagnostic Test: coronavirus (SARS-CoV-2) swab
Diagnostic Test: O2 saturation
Diagnostic Test: Complete Blood Count
Diagnostic Test: C-reactive protein
Diagnostic Test: Serum ferritin and D-dimer
Radiation: CT chest
Diagnostic Test: Liver and renal function tests

Study type

Observational

Funder types

Other

Identifiers

NCT06350526
PULMHEMA

Details and patient eligibility

About

Hematologic malignancies are heterogeneous groups of neoplasia, with frequent pulmonary complications. These complications may be secondary to the patient's comorbidities, to the hemopathy itself, or its treatments. Divided into infectious and non-infectious complications, the etiologies are numerous and varied. This makes the diagnostic approach complex for the clinicians

Full description

Although infectious processes of the lungs are common in these immunosuppressed patient collectives, non-infectious causes account for up to half of the pulmonary manifestations found in hematologic malignancies. Besides the frequent infections including opportunistic pathogens, a broad differential diagnosis including drug-induced lung injury by cytostatic substances, cytokines, and innovative immunotherapeutic agents, rarer transfusion of blood products, and intrathoracic manifestations of the hematologic malignancy itself, must be kept in mind. Finally, vascular complications can also lead to pulmonary reactions. Early and consistent diagnostics and treatment of bronchopulmonary, intrathoracic, and vascular complications within the framework of hematologic systemic diseases can be essential for the patient's prognosis. Up to 25% of patients with profound neutropenia lasting for >10 days develop lung infiltrates, which frequently do not respond to broad-spectrum antibacterial therapy. While a causative pathogen remains undetected in most cases, Aspergillus spp., Pneumocystis jirovecii, multi-resistant Gram-negative pathogens, mycobacteria or respiratory viruses may be involved. In at-risk patients who have received trimethoprim-sulfamethoxazole (TMP/SMX) prophylaxis, filamentous fungal pathogens appear to be predominant, yet commonly not proven at the time of treatment initiation.

In patients who do not improve rapidly with first-line therapy with broad spectrum antibiotics, cross-sectional thoracic CT imaging is essential. It provides much better definition of the pattern of radiological changes that includes three main groups: consolidation, nodules (micro- and macro-), and diffuse changes, as ground glass pattern. Discuss these radiological patterns and how this guides the appropriate initial investigations and treatment options will be of a great value to be followed.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients aged 18 years or older diagnosed with hematological diseases and documented pulmonary manifestations during their disease course

Exclusion criteria

  1. Patients aged under 18 years.
  2. Patients without demonstrable evidence of lung involvement.
  3. Patients with incomplete medical records or insufficient data to analyze.

Trial design

200 participants in 1 patient group

1
Description:
patient admitted with hematological disease and pulmonary manifestations
Treatment:
Radiation: CT chest
Diagnostic Test: Liver and renal function tests
Diagnostic Test: Serum ferritin and D-dimer
Diagnostic Test: C-reactive protein
Diagnostic Test: Complete Blood Count
Diagnostic Test: O2 saturation
Diagnostic Test: coronavirus (SARS-CoV-2) swab
Diagnostic Test: Lactate dehydrogenase

Trial contacts and locations

1

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Central trial contact

Asmaa N Hussein, MD

Data sourced from clinicaltrials.gov

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