High altitude pulmonary edema in a native highlander: A case report from Nepal

BACKGROUND: High altitude pulmonary edema (HAPE) is a non-cardiogenic pulmonary edema, that usually occurs in unacclimatized lowlanders rapidly ascending above 2,500-3,000 m and in highlanders returning from lower altitudes, with both forms likely sharing the same pathophysiology. Its incidence amo...

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Main Authors: Ishwor Thapaliya, Adesh Kantha, Krishna Datta Bhatta, Aakash Deo, Dilip Sharma Banjade, Sushil Kumar Yadav
Format: Article
Language:English
Published: University Library System, University of Pittsburgh 2025-01-01
Series:International Journal of Medical Students
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Online Access:http://ijms.info/IJMS/article/view/2972
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author Ishwor Thapaliya
Adesh Kantha
Krishna Datta Bhatta
Aakash Deo
Dilip Sharma Banjade
Sushil Kumar Yadav
author_facet Ishwor Thapaliya
Adesh Kantha
Krishna Datta Bhatta
Aakash Deo
Dilip Sharma Banjade
Sushil Kumar Yadav
author_sort Ishwor Thapaliya
collection DOAJ
description BACKGROUND: High altitude pulmonary edema (HAPE) is a non-cardiogenic pulmonary edema, that usually occurs in unacclimatized lowlanders rapidly ascending above 2,500-3,000 m and in highlanders returning from lower altitudes, with both forms likely sharing the same pathophysiology. Its incidence among Himalayan trekkers and Alp’s climbers is approximately 4%, often  varying with rate of ascent. It usually manifests within 2–4 days of arriving at altitudes exceeding 2,500 meters. The factors predisposing HAPE include prior respiratory infection, rapid ascent, prior history of HAPE, genetic predisposition. Patients with HAPE exhibit increased pulmonary artery pressures, normal left atrial pressure, heightened pulmonary vasoreactivity to hypoxia, and often benefit from treatments lowering pulmonary artery pressures. THE CASE: A 41-year-old male of Rai ethnicity, born and raised in the Himalayan region of Nepal began experiencing shortness of breath during his ascent of Mount Everest at around 5,000 meters. The individual, currently employed as a trekking porter, had previously descended to an altitude of 3,420 meters for 2 weeks before commencing his ascent. He reported to have progressively worsening shortness of breath. After the onset of symptoms, he started to descend during which he fell unconscious and was brought to a hospital in Lukla. He had a low Glasgow Coma Scale score of 3/15 and SpO2 could not be determined by pulse oximetry. At the hospital, he quickly regained consciousness after receiving supplemental oxygen. He was then referred to the tertiary care center in Kathmandu for further evaluation and treatment. At the emergency department, he reported progressive shortness of breath, worsening from MMRC grade II to IV, and orthopnea. He had a similar episode three years prior and no known co-morbidities. Vital signs were stable with oxygen saturation (SpO2) of 81% in ambient air. Physical examination revealed bilateral wheezes and crackles on chest auscultation. Neurological and abdominal examinations were normal. Laboratory analysis revealed neutrophilia (80%), lymphocytopenia (15%), leukocytosis (14,900 cells/mm³), elevated serum urea (9.4 mmol/l), and high Alanine Transaminase (86 U/l). Liver and renal function tests were normal. Arterial blood gas (ABG)  analysis revealed a low blood pH of 7.292. Sputum, blood, and urine cultures were negative for bacteria and fungi. He was transferred to the ICU for high-concentration oxygen therapy. ABG analysis was performed on a daily basis, with results illustrated in figure 1. He was intubated and mechanically ventilated for 4 days. Initially, chest x-ray was performed which shows pulmonary infiltrates in both lungs indicative of pulmonary edema as shown in figure 2. Throughout his ICU stay, he received iv antibiotics, CCBs and diuretics. By day 3, his crackles had significantly diminished, and a follow-up chest radiograph demonstrated notable improvement (Figure 3).  After 8 days, he was transferred to the respiratory medicine ward for 2 days of observation before discharge. CONCLUSION: Despite being physiologically adapted to high altitude conditions, native highlanders and people with prior history of HAPE may still be susceptible to developing high altitude pulmonary edema.
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spelling doaj-art-8b8c56ead93643eb8c66980849f21a302025-01-01T13:37:41ZengUniversity Library System, University of PittsburghInternational Journal of Medical Students2076-63272025-01-0112High altitude pulmonary edema in a native highlander: A case report from NepalIshwor Thapaliya0Adesh Kantha1Krishna Datta Bhatta2Aakash Deo3Dilip Sharma Banjade4Sushil Kumar Yadav5Institute of Medicine TU Teaching HospitalTribhuvan University, Institute of Medicine, Maharajgunj, 44600, NepalTribhuvan University, Institute of Medicine, Maharajgunj, 44600, NepalTribhuvan University, Institute of Medicine, Maharajgunj, 44600, NepalUniversal College of Medical Science, Bhairahawa, NepalTribhuvan University, Institute of Medicine, Maharajgunj, 44600, Nepal BACKGROUND: High altitude pulmonary edema (HAPE) is a non-cardiogenic pulmonary edema, that usually occurs in unacclimatized lowlanders rapidly ascending above 2,500-3,000 m and in highlanders returning from lower altitudes, with both forms likely sharing the same pathophysiology. Its incidence among Himalayan trekkers and Alp’s climbers is approximately 4%, often  varying with rate of ascent. It usually manifests within 2–4 days of arriving at altitudes exceeding 2,500 meters. The factors predisposing HAPE include prior respiratory infection, rapid ascent, prior history of HAPE, genetic predisposition. Patients with HAPE exhibit increased pulmonary artery pressures, normal left atrial pressure, heightened pulmonary vasoreactivity to hypoxia, and often benefit from treatments lowering pulmonary artery pressures. THE CASE: A 41-year-old male of Rai ethnicity, born and raised in the Himalayan region of Nepal began experiencing shortness of breath during his ascent of Mount Everest at around 5,000 meters. The individual, currently employed as a trekking porter, had previously descended to an altitude of 3,420 meters for 2 weeks before commencing his ascent. He reported to have progressively worsening shortness of breath. After the onset of symptoms, he started to descend during which he fell unconscious and was brought to a hospital in Lukla. He had a low Glasgow Coma Scale score of 3/15 and SpO2 could not be determined by pulse oximetry. At the hospital, he quickly regained consciousness after receiving supplemental oxygen. He was then referred to the tertiary care center in Kathmandu for further evaluation and treatment. At the emergency department, he reported progressive shortness of breath, worsening from MMRC grade II to IV, and orthopnea. He had a similar episode three years prior and no known co-morbidities. Vital signs were stable with oxygen saturation (SpO2) of 81% in ambient air. Physical examination revealed bilateral wheezes and crackles on chest auscultation. Neurological and abdominal examinations were normal. Laboratory analysis revealed neutrophilia (80%), lymphocytopenia (15%), leukocytosis (14,900 cells/mm³), elevated serum urea (9.4 mmol/l), and high Alanine Transaminase (86 U/l). Liver and renal function tests were normal. Arterial blood gas (ABG)  analysis revealed a low blood pH of 7.292. Sputum, blood, and urine cultures were negative for bacteria and fungi. He was transferred to the ICU for high-concentration oxygen therapy. ABG analysis was performed on a daily basis, with results illustrated in figure 1. He was intubated and mechanically ventilated for 4 days. Initially, chest x-ray was performed which shows pulmonary infiltrates in both lungs indicative of pulmonary edema as shown in figure 2. Throughout his ICU stay, he received iv antibiotics, CCBs and diuretics. By day 3, his crackles had significantly diminished, and a follow-up chest radiograph demonstrated notable improvement (Figure 3).  After 8 days, he was transferred to the respiratory medicine ward for 2 days of observation before discharge. CONCLUSION: Despite being physiologically adapted to high altitude conditions, native highlanders and people with prior history of HAPE may still be susceptible to developing high altitude pulmonary edema. http://ijms.info/IJMS/article/view/2972high altitude pulmonary edema, acclimatization, highlanders
spellingShingle Ishwor Thapaliya
Adesh Kantha
Krishna Datta Bhatta
Aakash Deo
Dilip Sharma Banjade
Sushil Kumar Yadav
High altitude pulmonary edema in a native highlander: A case report from Nepal
International Journal of Medical Students
high altitude pulmonary edema, acclimatization, highlanders
title High altitude pulmonary edema in a native highlander: A case report from Nepal
title_full High altitude pulmonary edema in a native highlander: A case report from Nepal
title_fullStr High altitude pulmonary edema in a native highlander: A case report from Nepal
title_full_unstemmed High altitude pulmonary edema in a native highlander: A case report from Nepal
title_short High altitude pulmonary edema in a native highlander: A case report from Nepal
title_sort high altitude pulmonary edema in a native highlander a case report from nepal
topic high altitude pulmonary edema, acclimatization, highlanders
url http://ijms.info/IJMS/article/view/2972
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AT adeshkantha highaltitudepulmonaryedemainanativehighlanderacasereportfromnepal
AT krishnadattabhatta highaltitudepulmonaryedemainanativehighlanderacasereportfromnepal
AT aakashdeo highaltitudepulmonaryedemainanativehighlanderacasereportfromnepal
AT dilipsharmabanjade highaltitudepulmonaryedemainanativehighlanderacasereportfromnepal
AT sushilkumaryadav highaltitudepulmonaryedemainanativehighlanderacasereportfromnepal