pneumothorax

What is pneumothorax

A pneumothorax is the medical term for what is commonly known as a collapsed lung with the presence of air or gas in the pleural cavity (the space between your lung and chest wall). A pneumothorax occurs when air leaks into the space between the lung and chest wall. This air in the pleural space can build up and pushes on the outside of your lung and makes it partially or fully collapse. A pneumothorax can be a complete lung collapse or a collapse of only a portion of the lung. In most cases, only some of the lung collapses. A pneumothorax is reasonably common and has many different causes. A pneumothorax can be caused by a blunt or penetrating chest injury, certain medical procedures, or damage from underlying lung disease. Or it may occur for no obvious reason called spontaneous pneumothorax.

Signs and symptoms of a pneumothorax include:

  • Chest pain on one side, especially when taking breaths.
  • Cough.
  • Fast breathing.
  • Fast heart rate.
  • Fatigue.
  • Shortness of breath (dyspnea).
  • Bluish skin, lips or nails (cyanosis).

If you have symptoms of a collapsed lung, go to the nearest emergency room. You may need immediate care.

Collapsed lung symptoms usually include sudden chest pain, shortness of breath with blue skin, nails or lips. On some occasions, a collapsed lung can be a life-threatening event.

The clinical results are dependent on the degree of collapse of the lung on the affected side. If the pneumothorax is significant, it can cause a shift of the mediastinum and compromise hemodynamic stability.

  • If you have a pneumothorax and you feel it is getting harder to breathe, call your local emergency number for an ambulance.

There are no direct figures on the incidence of pneumothorax. However, it is a common problem, frequently as a complication of trauma (often undiagnosed), and it also commonly occurs as a spontaneous occurrence and in patients with previous lung disease.

The goal in treating a pneumothorax is to relieve the pressure on your lung, allowing it to re-expand. Treatment options for a pneumothorax may include observation, needle aspiration, chest tube insertion, nonsurgical repair or surgery. You may receive supplemental oxygen therapy to speed air reabsorption and lung expansion. Depending on the cause of the pneumothorax, a second goal may be to prevent recurrences. The methods for achieving these goals depend on the severity of the lung collapse and sometimes on your overall health.

Treatment for a pneumothorax usually involves inserting a flexible tube or needle between the ribs to remove the excess air. However, a small pneumothorax may heal on its own.

Figure 1. Collapsed and normal lung

Collapsed and normal lung

Figure 2. A large, right-sided pneumothorax has occurred from a rupture of a subpleural bleb (chest X-ray).

pneumothorax

Figure 3. Large spontaneous pneumothorax

Large spontaneous pneumothorax

Footnotes: 35 year old male with symptoms of breathlessness on exertion and fatigue. On exam noted to have diminished air entry in the left lower lung base. Oxygen levels 97% at rest. Odd episodes of cough, lateral flow test negative. Chest X-ray showed large left sided pneumothorax with total collapse of the left lung. Minor mediastinal shift. Heart size normal. Right lung clear.

[Source 1 ]

Figure 4. Bilateral pneumothoraces

Bilateral pneumothoraces

Footnotes: 40 year old male with acute severe shortness of breath. No history of trauma. Chest X-ray large bilateral pneumothoraces. Although the costophrenic angles are excluded from the image, the deep sulcus sign is evident bilaterally.

[Source 2 ]

Figure 5. Spontaneous pneumothorax due to ruptured apical bullae 

Spontaneous pneumothorax due to ruptured apical bullae

Footnotes: 55 year old male with sudden severe breathlessness and right-sided pleuritic chest pain. Chest CT showed loculated pneumothorax due to pleural adhesions. Apical lung bullae or blebs that predispose to spontaneous pneumothorax. These blebs are not on the background of bullous emphysema.

[Source 3 ]

How common is spontaneous pneumothorax?

Spontaneous pneumothorax occurs more frequently in adults than children and more frequently in males than females 4. Spontaneous pneumothorax is a common clinical presentation, with 14.1 admissions per 100 000 people per year aged ≥15 years 5. In the United States, the adult incidence of primary spontaneous pneumothorax is estimated to be 7.4 per 100,000 to 18 per 100,000 people per year in males and 1.2 per 100,000 to 6.0 per 100,000 people per year in females, with similar rates of secondary spontaneous pneumothorax in males and females, 6.3 and 2.0 per 100,000 people per year, respectively 4. In children, the combined incidence of spontaneous pneumothorax is estimated to be 4.0 per 100,000 children per year in males and 1.1 per 100,000 children per year in females. Other risk factors include a history of smoking, and a tall, thin body habitus 6, 7.

What is a small and large pneumothorax?

Estimating the size of pneumothorax is somewhat controversial with no international consensus. Chest CT scan is considered more accurate than plain chest X-ray.

British Thoracic Society (BTS) guidelines (2010) measured from chest wall to lung edge at the level of the hilum 8:

  • <2 cm: Small
  • ≥2 cm: Large

American College of Chest Physicians guidelines (ACCP) measured from thoracic cupola to lung apex 9:

  • <3 cm: Small
  • ≥3 cm: Large

Expert group considers a pneumothorax as large when there is a visible rim along the entire axillary line, ≥ 2 cm between the lung margin and the chest wall at the hilum level 10.

Figure 6. Large pneumothorax size

Large pneumothorax size

Footnotes: Estimation of size of a pneumothorax based on routine chest X-ray. (a) The American College of Chest Physicians (ACCP) generally use the intrapleural distance from the apex to the cupola of the lung, whereas the British Thoracic Society (BTS) uses the intrapleural distance at the hilum (b).

[Source 11 ]

How serious is a pneumothorax?

The seriousness of a pneumothorax depends on the cause and how much of your lung is collapsed. Some cases aren’t serious, and some are medical emergencies. Pneumothorax can be caused by a variety of health problems, and some can be life-threatening, so seek medical attention. If your chest pain is severe or breathing becomes increasingly difficult, get immediate emergency care.

Your doctor can tell you how much of your lung is collapsed and what your treatment options are. The goal in treating a pneumothorax is to relieve the pressure on your lung, allowing it to re-expand. Treatment options may include observation, needle aspiration, chest tube insertion, nonsurgical repair or surgery. You may receive supplemental oxygen therapy to speed air reabsorption and lung expansion.

How long does it take for a pneumothorax to heal?

If the pneumothorax is small, the leak usually heals itself and the trapped air is gradually absorbed by your body. This normally takes 1 to 2 weeks. You can use over-the-counter painkillers to manage your pain and you might also be given oxygen.

What is the recurrence rate of primary spontaneous pneumothorax?

Primary spontaneous pneumothorax recurrence rates vary widely in the published literature, with limited data describing the factors that influence recurrence. This systematic review showed a 32% recurrence rate in primary spontaneous pneumothorax, with greatest risk in the first year 12. There are no established factors that predict pneumothorax recurrence and consequently no method for risk-stratifying patients. Female sex, low body weight (lower BMI), smoking and height in males have all been postulated as risk factors for higher risk of pneumothorax recurrence 13, 14, 15, 16. Certain radiographic features have also been suggested to confer additional risk, including bullae on computed tomography (CT) and pleural thickening on chest radiography 17, 18, 19. Importantly, there is no consensus on which treatment offers the greatest reduction in risk of pneumothorax recurrence 20, 21, 22, 23.

Is chest tube drainage superior to conservative strategy?

A single study has assessed the conservative strategy in patients with a first episode of a large unilateral primary spontaneous pneumothorax 24. This multicenter, open-label, randomized controlled trial included 316 patients aged 14 to 50 years: 154 in the chest tube drainage and hospitalization (“standard”) arm and 162 in the conservative strategy arm.

The conservative management was non-inferior to the “standard” management on the primary endpoint (eight weeks radiographic resolution) 24. The risk of ipsilateral recurrence at one year was lower in the conservative arm (8.8% vs 16.8%) 24, 20. However, these data should be considered with caution as 1-year recurrence rate was lower than usual in both arms, 29% in the meta-analysis by Walker et al 25. The conservative strategy allowed reducing the number of procedures (percutaneous pleural procedures, need for surgery, imaging), the hospital length of stay, the rate of adverse events and the number of days out of work 24. The failure rate of the conservative strategy (defined as the need for chest tube drainage) ranged between 15 and 21% 24, 26.

However, some biases limit its conclusions, rending questionable and hardly generalizable these results:

  • In sensitivity analyzes, if all lost to follow-up patients are considered as “failures”, the difference in success at eight weeks exceeds the non-inferiority limit and the study is negative, with conservative management less effective than chest tube drainage;
  • There might be an inclusion bias, as only 316 patients out of the 2637 screened were included;
  • The type of included patients seems unusual: the duration of primary spontaneous pneumothorax evolution was about of 40 hours, the patients being barely asymptomatic (median dyspnea and pain visual analog scale scores respectively of 1 and 2 on 10-points scales).

Further studies are needed to assess the safety and better define the profile of patients who could benefit from a conservative strategy.

Is chest tube drainage superior to needle aspiration?

Needle aspiration requires a transient pleural approach, performed until bubbling stops 27, 28, until aspiration is no longer possible 29, 30, until a fixed volume is aspirated 31, 30, 32 or for a maximal time 27, 28, 29. If needle aspiration is not sufficient, studies suggest either switching to chest tube drainage 33, 28, 34, 35, 36 or to attempt a second (or a third) needle aspiration 27, 28, 29, 37, although not recommended 38, 39. Needle aspiration failure is defined as an attempted needle aspiration followed by a chest tube drainage 27, 34, 35, 36, 37.

Chest tube drainage shows a higher “immediate success” rate compared to needle aspiration 27, 40, 30, 41, 42. A later success rate (at day 7 or later), appears similar between chest tube drainage and needle aspiration 29, 43, 40, 32, 44. The overall immediate success rate is 51% for needle aspiration (after 1 − 3 procedures) and about 68% for chest tube drainage 27, 29, 31, 43, 32, 37, 45.

Needle aspiration reduces the hospital length of stay compared chest tube drainage (i.e. with hospitalization) 27, 29, 31, 43, 32, 37, 45, 46, 42.

Needle aspiration allowed decreasing drainage duration compared to chest tube drainage in an randomized controlled trial 32.

The risk of complications is rarely reported and lower during needle aspiration than chest tube drainage 29, 30, 44. One study found similar complication rates between needle aspiration and chest tube drainage 37.

Conflicting data exist in pain. Although some report less pain with needle aspiration 29, 44 and higher analgesic use in chest tube drainage 29, older studies did not report any difference between techniques 27, 37.

Treatment satisfaction did not differ between needle aspiration and chest tube drainage 37.

Surgery rate did not differ between needle aspiration and chest tube drainage 37, 32. A single old study, of low level of evidence, reported a more frequent need for pleurectomy in chest tube drainage as compared to needle aspiration 31.

Costs had not been analyzed in these studies. The 2017 Cochrane Database considered that no conclusion was possible 47. However, as needle aspiration reduces the hospital length of stay as compared to chest tube drainage, the cost of such management would be lower. Dedicated medico-economic studies are needed.

One-year (and sometimes 3 months) recurrence rates did not differ between needle aspiration and chest tube drainage 27, 29, 31, 43, 40, 41, 44, 45.

Based on these findings, needle aspiration might appear superior to chest tube drainage. Given the possibility of an outpatient management with a chest tube drainage, these two approaches were kept as first-line management of large primary spontaneous pneumothorax.

Is chest tube drainage superior to surgery?

Seventy percent of patients with a first primary spontaneous pneumothorax will never relapse. Therefore, performing surgery at first episode of primary spontaneous pneumothorax seems too invasive 25. However, several studies compared surgical treatment (pleurodesis and bleb removal) following chest tube drainage or needle aspiration to a conventional chest tube drainage strategy without surgery during a first episode of large primary spontaneous pneumothorax. These studies reported a reduced one-year risk of recurrence, a shorter length of stay, a lower cost and no difference in analgesic for surgically treated patients compared to conventional chest tube drainage 48, 49, 50, 51, 52, 53. These studies had several biases drawing the conclusion was not easy.

Is outpatient superior to inpatient management?

No high-quality study has directly compared the outpatient management with needle aspiration versus mini-chest tube drainage with one-way valve. At least one such study is ongoing (PNEUM-AMBU, NCT03691480) 54.

Exclusive outpatient management is feasible in 4 out of 5 patients treated with needle aspiration or chest tube drainage with a one-way valve 55, 56, 57.

Compared with inpatient care, outpatient management reduces the hospital length of stay, as reported in a study comparing a drainage system with an integrated one-way valve versus a standard management with needle aspiration in most cases (68% of patients in the control arm) 57. In most other publications, outpatient needle aspiration has been compared to drainage with hospital-based monitoring. Series reporting outpatient management have also suggested a reduced hospital length of stay but without control arm 58, 56, 55, 59.

Use of surgery was not assessed specifically in study reporting outpatient strategy.

Outpatient management could increase the complications rates as compared to inpatient management 57. However, the design of this prospective study explains most of the severe complications, as adverse events were defined as the need for hospitalization, which could only concern patients of the outpatient arm.

On the other hand, in observational studies, no serious adverse events were reported, but mainly bent or displaced catheters (ranging from 1.5% to 22.6%) 58, 56, 55, 59.

Outpatient management was associated with a similar 1-year recurrence rate as inpatient management, ranging from 12% to 33.1% 58, 56, 55, 59, 55.

Indirect evidence suggest a lower overall health care costs of outpatient management 58, 56.

Expert group recommends outpatient management in patients with large primary spontaneous pneumothorax without signs of immediate severity 10.

The expert group recommends an outpatient management based on needle aspiration or on mini-chest tube with one-way valve, if the following criteria are met 10:

  • the patient is stable after intrapleural air removal,
  • and a dedicated outpatient care system is previously organized
  • and a consultation with chest ultrasound or chest X-ray is scheduled at 24−72 hour to assess the evolution.

The expert group proposes outpatient management of primary spontaneous pneumothorax only if all of the following conditions are met 10:

  • A patient information leaflet providing guidance on the way to behave in case of problem and phone numbers available 24/7, is given to the patient before hospital discharge,
  • Patient’s comprehension of discharge instructions has been checked
  • The patient should not stay alone for the first 24 − 48 hour after being discharged home,
  • The patient should be able to access a medical facility within 1 hour, regardless of the means of transportation, in the event of deterioration,
  • The time of discharge does not matter if all of the above criteria are met (nighttime discharge is possible).

Chest anatomy

Your chest cavity also called the thoracic cavity is formed by the ribs, the muscles of the chest, the sternum (breastbone), and the thoracic portion of the vertebral column. Within your thoracic cavity are 3 smaller cavities: (a) 2 pleural cavities (fluid-filled spaces one around each lung), your left pleural cavity (holds your left lung) and your right pleural cavity (holds your right lung) and (b) a central portion of your thoracic cavity between your lungs called the mediastinum (media- = middle; -stinum = partition). The mediastinum is the central portion of your thoracic cavity between your lungs, extending from the base of your neck (from your first rib and sternum) to the diaphragm. The mediastinum contains your heart (pericardial cavity, peri- = around; -cardial = heart, a fluid-filled space that surrounds your heart), the major blood vessels connected to your heart and lungs, the trachea (windpipe) and bronchi, the esophagus (foodpipe), the thymus, and lymph nodes but not your lungs. Your right and left lungs are on either side of the mediastinum. The diaphragm is a dome-shaped muscle that separates the thoracic cavity from the abdominopelvic cavity.

Your mediastinum is divided into several parts, which researchers call compartments. The traditional or classical model divides your mediastinum into four parts:

  • Superior mediastinum: The top part, located superior to (above) your heart.
  • Anterior mediastinum: The part anterior to (in front of) your heart, between your heart and your sternum (breastbone).
  • Middle mediastinum: The part that contains your heart.
  • Posterior mediastinum: The part posterior to (behind) your heart.

A membrane is a thin, pliable tissue that covers, lines, partitions, or connects internal organs (viscera). One example is a slippery, double-layered membrane associated with body cavities that does not open directly to the exterior called a serous membrane. Serous membrane covers your internal organs (viscera) within the thoracic and abdominal cavities and also lines the walls of the thorax and abdomen. The parts of a serous membrane are (1) the parietal layer (outer layer), a thin epithelium that lines the walls of the cavities, and (2) the visceral layer (inner layer), a thin epithelium that covers and adheres to the viscera within the cavities. Between the two layers is a potential space that contains a small amount of lubricating fluid (serous fluid). The fluid allows the internal organs (viscera) to slide somewhat during movements, such as when the lungs inflate and deflate during breathing.

Within the right and left sides of your thoracic cavity (chest cavity), the compartments that contain your lungs, on either side of the mediastinum, are lined with a membrane called the parietal pleura (outer serous membrane) lining the inside of your rib cage (parietal pleura lines the chest wall) and covering the superior surface of the diaphragm. A similar membrane, called the visceral pleura (inner serous membrane), clings to the surface of your lungs forming the external surface of your lung. The visceral (inner) and parietal (outer) pleural membranes are separated only by a thin film of watery fluid called serous fluid, which is secreted by the parietal and visceral pleural membranes. Although no actual space normally exists between the parietal (outer) and visceral (inner) pleural membranes, the potential space between them is called the pleural cavity. The parietal pleura (outer membrane) and visceral pleura (inner membrane) slide with little friction across the cavity walls as your lungs move, expand and collapse during respiration.

Your heart, which is located in the broadest portion of the mediastinum, is surrounded by pericardial membranes called the pericardium. Your pericardium is a protective, fluid-filled sac that surrounds your heart and helps it function properly.

Your respiratory system includes the trachea, the right and left lungs and their lobes, and the bronchi. Oxygen (O2) is inhaled into your lungs and passes through the alveoli (the tiny air sacs at the end of the bronchioles) and into your bloodstream, where it travels to the tissues throughout the body.

Figure 7. Chest anatomy

thoracic cavity

Figure 8. Thoracic cavity

Thoracic cavity

Footnote: The black dashed lines indicate the borders of the mediastinum.

Figure 9. Thoracic cavity transverse section

thoracic cavity transverse section

Figure 10. Mediastinum

Mediastinum

Figure 11. Respiratory system

respiratory system

The Lungs

The lungs (= lightweights, because they float) are paired cone-shaped, soft, spongy organs in the thoracic (chest) cavity (Figure 1). The lungs consist largely of air tubes and spaces. The balance of the lung tissue, its stroma, is a framework of connective tissue containing many elastic fibers. As a result, the lungs are light, soft, spongy, elastic organs that each weigh only about 0.6 kg (1.25 pounds). The elasticity of healthy lungs helps to reduce the effort of breathing. The lungs are separated from each other by the heart and other structures of the mediastinum, which divides the thoracic cavity into two anatomically distinct chambers. As a result, if trauma causes one lung to collapse, the other may remain expanded.

Each lung is enclosed and protected by a double-layered serous membrane called the pleural membrane or pleura. The superficial layer, called the parietal pleura, lines the wall of the thoracic cavity; the deep layer, the visceral pleura, covers the lungs themselves (Figures 2 and 3). Between the visceral and parietal pleurae is a small space, the pleural cavity, which contains a small amount of lubricating fluid secreted by the membranes. This pleural fluid reduces friction between the membranes, allowing them to slide easily over one another during breathing. Pleural fluid also causes the two membranes to adhere to one another just as a film of water causes two glass microscope slides to stick together, a phenomenon called surface tension. Separate pleural cavities surround the left and right lungs. The left and right lungs are situated in the left and right pleural cavities inside the thoracic cavity.

A lung will collapse if air enters the pleural cavity, a condition called pneumothorax. The air breaks the seal of pleural fluid that holds the lung to the thoracic wall, allowing the elastic lung to collapse like a deflating balloon.

Inflammation of the pleural membrane, called pleurisy or pleuritis, may in its early stages cause pain due to friction between the parietal and visceral layers of the pleura. If the inflammation persists, excess fluid accumulates in the pleural space, a condition known as pleural effusion.

Below the lungs, a thin, dome-shaped muscle called the diaphragm separates the chest from the abdomen. When you breathe, the diaphragm moves up and down, forcing air in and out of the lungs. The thoracic cage encloses the rest of the lungs.

Figure 12. Lung anatomy

Lung anatomy
lungs anatomy

Figure 13. Lungs pleural cavity

lung pleural cavity

Figure 14. Bronchial tree of the lungs
trachea-bronchus-lungs

Types of pneumothorax

There are different types of pneumothorax:

Spontaneous pneumothorax

Spontaneous pneumothorax is a collapsed lung that happens without an injury. Spontaneous pneumothorax types include:

Primary spontaneous pneumothorax

Primary spontaneous pneumothorax is the most common type of pneumothorax, has no known cause and develops in otherwise healthy people. Primary spontaneous pneumothorax is thought to be caused by a tiny tear of an outer part of the lung. This can happen if abnormal air pockets in your lung (blebs) break apart and release air. Primary spontaneous pneumothorax is more common in tall people and mainly affects healthy young adults without lung disease.

Secondary spontaneous pneumothorax

Secondary spontaneous pneumothorax develops as a complication of existing lung disease, such as chronic obstructive pulmonary disease (COPD), pneumonia, tuberculosis, sarcoidosis or cystic fibrosis. The lung disease weakens the edge of the lung in some way, making the lung more likely to tear and cause air to escape.

Catamenial pneumothorax

Catamenial pneumothorax is a pneumothorax occurring during the perimenstrual period that affect women with endometriosis 60. “Perimenstrual period” encompasses the period of 72 – 96 hours before and after menstrual bleeding. Endometrial tissue growing outside of your uterus can form cysts that can bleed into the pleural space, causing your lung to collapse.

The broadest definitions of catamenial pneumothorax describe it as pneumothorax occurring from 7 days before the start of monthly bleeding to 7 days after its completion 61. The additional criteria include: characteristic pleural lesions, right-sided location of the pneumothorax, and concomitant endometriosis 62, 63. Concomitance of catamenial pneumothorax and endometriosis was described in a woman in the 8th week of pregnancy 64. Thoracic endometriosis is defined as the presence of ectopic endometrium within the chest, the symptoms of which appear during ovulation 65. Symptoms of pelvic endometriosis, secondary or primary infertility, and previous gynecological procedures 62 may suggest the diagnosis of catamenial pneumothorax in the course of endometriosis. A review of the treatment results of 110 patients with thoracic endometriosis revealed that pneumothorax occurred in 72% of the women, hemoptysis in 14%, pleural hematomas in 12%, and lung nodules in 2% 65. Pelvic endometriosis may precede the development of thoracic endometriosis by 5 years 66. Despite the fact that the most common manifestation of thoracic endometriosis is pneumothorax 65, in some cases of catamenial pneumothorax, endometrial character of the disease cannot be confirmed histologically 61. Abnormal fenestrations in the tendinous part of the diaphragm can be observed during surgical procedures performed on patients suffering from catamenial pneumothorax concomitant with endometriosis. Furthermore, the patients’ pleurae feature spots and nodules which are endometrial implants. The lesions are most often located on the diaphragmatic pleura.

3% to 6% of spontaneous pneumothorax cases meet the definition of catamenial pneumothorax, constituting an indication for surgical treatment in 1/3 of the affected women. The mean age of onset is 32-35 years 67. The condition may develop as late as at 39 years of age 68. Catamenial pneumothorax is most often (85-95%) unilateral, occurring on the right side of the chest, but it may also occur on the left side or bilaterally 68.

The cause and subsequent development of catamenial pneumothorax is explained by the following theories: physiological, migrational, microembolic-metastatic, and the diaphragmatic theory of air “passage” (Table 1).

Catamenial pneumothorax is associated with the following findings: single or multiple fenestrations in the tendinous part of the diaphragm; red/brown spots or nodules located on the diaphragmatic or visceral pleura. Histopathological analysis of these nodules (spots) reveals glandular cells, endometrial stroma, and macrophages filled with hemosiderin, whereas immunohistochemical testing may demonstrate the presence of estrogen and progesterone receptors 69. These findings are observed if pneumothorax is accompanied by endometriosis, especially within the pelvis, as occurs in 30-51% of cases.

Table 1. Theories for the development of thoracic foci of endometriosis in the development of catamenial pneumothorax

PhysiologicalHigh concentration of prostaglandin F2 during menses may cause blood vessels and bronchioles to contract, which leads to alveolar rupture and development of pneumothorax.
MigrationalEndometrial cells may migrate from the uterus, through the fallopian tubes, into the lesser pelvis and further, into the area of the diaphragm. The cyclical proliferation and necrosis of endometrial cells may injure the diaphragm, enabling the cells to migrate further into the chest and the visceral pleura, which may lead to pulmonary alveolar injury and pneumothorax.
Microembolic-metastaticMetastatic spread or pulmonary microembolization from endometrial cells through blood or lymph vessels. Necrosis of subpleural interstitial endometriotic foci leads to pneumothorax; foci located more centrally cause hemoptysis.
Diaphragmatic theory of air “passage”Air passes through the uterus and fallopian tubes into the peritoneal cavity and, through diaphragmatic fenestrations, into the pleural cavity.
[Source 60 ]

Traumatic pneumothorax

Traumatic pneumothorax is a type of pneumothorax is caused by an incident such as a car accident, broken ribs or a stab wound.

Iatrogenic pneumothorax

Iatrogenic pneumothorax is a pneumothorax that occurs as a result of mechanical ventilation, which causes an imbalance in the air pressure around the lungs. Iatrogenic pneumothorax is also caused by a medical procedure when your lung is punctured during a lung biopsy or a central venous line insertion.

Tension pneumothorax

Tension pneumothorax is a pneumothorax (of any type) when air can get into your lungs but can’t get out. The one-way valve effect causes pressure to build up inside of your chest that could lead to your heart and lungs not working properly. Tension pneumothorax is a serious form of pneumothorax that’s a medical emergency.

Progression of pneumothorax

Excluding that caused by chest trauma, pneumothorax arises due to rupture of alveoli, followed by rupture of the pleural lining of the lung. Provided this communication then seals itself off, air in the pleural space is gradually resorbed. If the communication between the pleural space and the airways remains open, a ‘bronchopleural fistula’ is created.

Rarely, the communication remains open, but the defect acts as a flap valve, allowing air into the pleural space on inspiration, but preventing it from escaping during expiration. Thus, air accumulates in the pleural space with each breath, compressing adjacent lung, and eventually compressing other structures in the chest, including the heart. This is called ‘tension pneumothorax’. Tension pneumothorax rarely occurs spontaneously.

Pneumothorax prognosis (outlook)

Tension pneumothorax is a potentially life-threatening condition, due to restriction of venous return, and respiratroy and cardiac shock. Otherwise, pneumothorax tends to slowly resolve, such that a pneumothorax causing 50% collapse of the lung will take 40 days to heal.

Pneumothorax complications

Many people who have had one pneumothorax can have another, usually within one to two years of the first. Air may sometimes continue to leak if the opening in the lung won’t close. Surgery may eventually be needed to close the air leak.

Although most collapsed lungs heal without issues, some people have serious complications. These can include:

  • Re-expansion pulmonary edema.
  • Damage or infection caused by the treatment.
  • Respiratory failure.
  • Heart failure.

Pneumothorax causes

A pneumothorax can be caused by:

  • Chest injury. Any blunt or penetrating injury to your chest can cause lung collapse. Some injuries may happen during physical assaults (gunshot wound, stab wound) or car crashes, while others may inadvertently occur during medical procedures that involve the insertion of a needle into your chest for a nerve block, lung biopsy or central venous line placement.
  • Lung disease. Damaged lung tissue is more likely to collapse. Lung damage can be caused by many types of underlying diseases, including chronic obstructive pulmonary disease (COPD), cystic fibrosisasthma, pneumoniatuberculosis, idiopathic pulmonary fibrosis, emphysema, lung canceracute respiratory distress syndrome (ARDS), lymphangioleiomyomatosis or collagen vascular disease (a group of autoimmune disorders that cause the body’s immune system to attack its own tissues).
  • Ruptured air blisters. Small air blisters (blebs) can develop on the top of your lung. These blebs sometimes burst — allowing air to leak into the space that surrounds the lungs.
  • Mechanical ventilation. A severe type of pneumothorax can occur in people who need mechanical assistance to breathe. The ventilator can create an imbalance of air pressure within the chest. The lung may collapse completely.
  • Lifestyle factors such as drug use, especially inhaled drugs, smoking, flying that involves drastic changes in air pressure or scuba or deep-sea diving.

Risk factors for a pneumothorax

Pneumothorax in those over 40 years of age is commonly seen in the background of emphysema or chronic bronchitis. Occasionally, asthma, and other lung disease can cause a pneumothorax.

In younger patients, pneumothorax may occur spontaneously or due to chest trauma. Spontaneous pneumothorax commonly occurs in tall, thin young men (sex ratio: 6:1), due to rupture of small subpleural ‘blebs’. Trauma such as a rib fracture, or penetrating chest wall injury, may also cause pneumothorax.

Risk factors for a pneumothorax include:

  • Your sex. In general, men are far more likely to have a pneumothorax than are women.
  • Smoking. The risk increases with the length of time and the number of cigarettes smoked, even without emphysema.
  • Age. The type of pneumothorax caused by ruptured air blisters is most likely to occur in people between 20 and 40 years old, especially if the person is a very tall and underweight.
  • Genetics. Certain types of pneumothorax appear to run in families.
  • Lung disease. Having an underlying lung disease — especially chronic obstructive pulmonary disease (COPD) — makes a collapsed lung more likely.
  • Mechanical ventilation. People who need mechanical ventilation to assist their breathing are at higher risk of pneumothorax.
  • Previous pneumothorax. Anyone who has had one pneumothorax is at increased risk of another, usually within one to two years of the first.
  • Pregnancy
  • Have a tall, thin body type, especially if you are a man.
  • Marfan syndrome.
  • Endometriosis.

Pneumothorax signs and symptoms

The presentation of patients with pneumothorax varies depending on the types of pneumothorax and ranges from completely asymptomatic to life-threatening respiratory distress:

  • Spontaneous pneumothorax: No clinical signs or symptoms in primary spontaneous pneumothorax until a bleb ruptures and causes pneumothorax; typically, the result is acute onset of chest pain and shortness of breath, particularly with secondary spontaneous pneumothoraces
  • Iatrogenic pneumothorax: Symptoms similar to those of spontaneous pneumothorax, depending on patient’s age, presence of underlying lung disease, and extent of pneumothorax
  • Tension pneumothorax: Hypotension, hypoxia, chest pain, dyspnea
  • Catamenial pneumothorax: Women aged 30-40 years with onset of symptoms within 48 hours of menstruation, right-sided pneumothorax, and recurrence
  • Pneumomediastinum: Must be differentiated from spontaneous pneumothorax; patients may or may not have symptoms of chest pain, persistent cough, sore throat, dysphagia, shortness of breath, or nausea/vomiting.

The main symptoms of a pneumothorax are sudden chest pain and shortness of breath. But these symptoms can be caused by a variety of health problems, and some can be life-threatening. If your chest pain is severe or breathing becomes increasingly difficult, get immediate emergency care.

Spontaneous and iatrogenic pneumothorax

Until a bleb ruptures and causes pneumothorax, no clinical signs or symptoms are present in primary spontaneous pneumothorax. Young and otherwise healthy patients can tolerate the main physiologic consequences of a decrease in vital capacity and partial pressure of oxygen fairly well, with minimal changes in vital signs and symptoms, but those with underlying lung disease may have respiratory distress.

In one series, acute onset of chest pain and shortness of breath were present in all patients in one series; typically, both symptoms are present in 64-85% of patients. The chest pain is described as severe and/or stabbing, radiates to the ipsilateral (same side) shoulder and increases with inspiration (pleuritic).

In primary spontaneous pneumothorax, chest often improves over the first 24 hours, even without resolution of the underlying air accumulation. Well-tolerated primary spontaneous pneumothorax can take 12 weeks to resolve. In secondary spontaneous pneumothorax, the chest pain is more likely to persist with more significant clinical symptoms.

Shortness of breath/dyspnea in primary spontaneous pneumothorax is generally of sudden onset and tends to be more severe with secondary spontaneous pneumothorax because of decreased lung reserve. Anxiety, cough, and vague presenting symptoms (e.g, general malaise, fatigue) are less commonly observed. The most common underlying abnormality in secondary spontaneous pneumothorax is chronic obstructive pulmonary disease (COPD), and cystic fibrosis carries one of the highest associations, with more than 20% reporting spontaneous pneumothorax.

Despite descriptions of Valsalva maneuvers and increased intrathoracic pressures as inciting factors, spontaneous pneumothorax usually develops at rest. By definition, spontaneous pneumothorax is not associated with trauma or stress. Symptoms of iatrogenic pneumothorax are similar to those of a spontaneous pneumothorax and depend on the age of the patient, the presence of underlying lung disease, and the extent of the pneumothorax.

A history of previous pneumothorax is important, as recurrence is common, with rates reported between 15% and 40%. Up to 15% of recurrences can be on the contralateral (opposite) side. Secondary pneumothoraces are often more likely to recur, with cystic fibrosis carrying the highest recurrence rates at 68-90%. No study has shown that the number or size of blebs and bullae found in the lung can be used to predict recurrence.

Tension pneumothorax

Signs and symptoms of tension pneumothorax are usually more impressive than those seen with a simple pneumothorax, and clinical interpretation of these is crucial for diagnosing and treating the condition. Tension pneumothorax is classically characterized by hypotension (low blood pressure) and hypoxia (low blood oxygen). On examination, breath sounds are absent on the affected hemothorax and the trachea deviates away from the affected side. The thorax may also be hyperresonant; jugular venous distention and tachycardia may be present. If on mechanical ventilation, the airway pressure alarms are triggered.

Because of subtle presentations that do not always present with the classically described clinical findings of this condition or the complexity of the patient with critical illness or injury to describe a tension pneumothorax, actual case reports include descriptions of the diagnosis of the condition being missed or delayed.  Nevertheless, tension pneumothorax should always be a consideration when acute compromise occurs.

Symptoms of tension pneumothorax may include chest pain (90%), dyspnea (80%), anxiety, fatigue, or acute epigastric pain (a rare finding).

Catamenial pneumothorax

The symptoms of catamenial pneumothorax are typical of spontaneous pneumothorax, but the condition may also be asymptomatic.

Women aged 30-40 years who present with onset of symptoms within 48 hours of menstruation, right-sided pneumothorax, and recurrence raise suspicion for catamenial pneumothorax.

Pneumomediastinum

Pneumomediastinum must be differentiated from spontaneous pneumothorax. Patients may or may not have symptoms, as this is typically a well-tolerated disease, although mortality in cases of esophageal rupture is very high.

This condition usually occurs when intrathoracic pressures become elevated, such as with an exacerbation of asthma, coughing, vomiting, childbirth, seizures, and a Valsalva maneuver. In many patients who present with pneumomediastinum, it occurs as a result of endoscopy and small esophageal perforation.

In a retrospective review of cases presenting to an academic medical center, 67% of identified patients had chest pain; 42% had persistent cough; 25% had sore throat; and 8% had dysphagia, shortness of breath, or nausea/vomiting.

Other symptoms may include substernal chest pain, usually radiating to the neck, back, or shoulders and exacerbated by deep inspiration, coughing, or supine positioning; dyspnea; neck or jaw pain; dysphagia, dysphonia, and/or abdominal pain (unusual symptoms).

Traumatic mediastinum, although present in up to 6% of patients, does not portend serious injury 70.

Pneumothorax diagnosis

If you have a sudden onset of shortness of breath or sharp chest pain that is worsened by breathing, go to the Emergency Room to be evaluated or call your local emergency number. In order to make an accurate diagnosis, the medical team will evaluate your symptoms and perform a physical exam, including the following:

  • History: Your physician will obtain your full medical history, in addition to assessing the symptoms you’re currently experiencing. You may be asked questions about when the symptoms started, the severity of the pain or shortness of breath, and length of time you waited prior to arriving to the Emergency Room.
  • Physical exam: Using a stethoscope, your doctor will listen for decreased or no breath sounds on the affected side.
  • Chest X-ray: This radiologic test will show a pneumothorax if it is present. Perform frontal chest X-ray in inspiration, without expiratory films, in case of suspected spontaneous pneumothorax to diagnose it and assess its size.
  • In some cases, a chest computerized tomography (CT) scan (low-dose chest CT-scan) may be needed to provide more-detailed images. The chest CT-scan is superior to the chest X-ray for assessing the size of a pneumothorax and to determine secondary pneumothorax causes 71. However, the cost, time and radiation exposure do not support its use as a first-line examination.
  • Chest ultrasound imaging also may be used to identify a pneumothorax. The added value of chest ultrasound is currently for chest trauma patients or the diagnosis of iatrogenic pneumothorax, with a high pretest probability 72, 73.

Physical Examination

The presentation of a patient with pneumothorax may range from completely asymptomatic to life-threatening respiratory distress. Symptoms may include diaphoresis, splinting chest wall to relieve pleuritic pain, and cyanosis (in the case of tension pneumothorax). Findings on lung auscultation also vary depending on the extent of the pneumothorax. Affected patients may also reveal altered mental status changes, including decreased alertness and/or consciousness (a rare finding).

Respiratory findings may include the following:

  • Respiratory distress (considered a universal finding) or respiratory arrest
  • Tachypnea (or bradypnea as a preterminal event)
  • Asymmetric lung expansion – A mediastinal and tracheal shift to the contralateral side can occur with a large tension pneumothorax
  • Distant or absent breath sounds – Unilaterally decreased or absent lung sounds is a common finding, but decreased air entry may be absent even in an advanced state of the disease
  • Lung sounds transmitted from the unaffected hemithorax are minimal with auscultation at the midaxillary line
  • Hyperresonance on percussion – This is a rare finding and may be absent even in an advanced state of the disease
  • Decreased tactile fremitus
  • Adventitious lung sounds (crackles, wheeze; an ipsilateral finding)

Cardiovascular findings may include the following:

  • Tachycardia – This is the most common finding. If the heart rate is faster than 135 beats/min, tension pneumothorax is likely
  • Pulsus paradoxus
  • Hypotension – This should be considered as an inconsistently present finding; although hypotension is typically considered a key sign of a tension pneumothorax, studies suggest that hypotension can be delayed until its appearance immediately precedes cardiovascular collapse
  • Jugular venous distention – This is generally seen in tension pneumothorax, although it may be absent if hypotension is severe
  • Cardiac apical displacement – This is a rare finding

Spontaneous and iatrogenic pneumothorax

Signs of spontaneous and iatrogenic pneumothorax are similar and depend on the underlying lung disease and extent of the pneumothorax. Tachycardia is the most common finding, and tachypnea and hypoxia may be present.

Tension pneumothorax

Although tension pneumothorax may be a difficult diagnosis to make and may present with considerable variability in signs, respiratory distress and chest pain are generally accepted as being universally present, and tachycardia and ipsilateral air entry on auscultation are also common findings. Sometimes, reliance on history alone may be warranted.

Findings may be affected by the volume status of the patient. In hypovolemic trauma patients with ongoing hemorrhage, the physical findings may lag behind the presentation of shock and cardiopulmonary collapse. Increased pulmonary artery pressures and decreased cardiac output or cardiac index are evidence of tension pneumothorax in patients with Swan-Ganz catheters.

When examining a patient for suspected tension pneumothorax, any clue may be helpful, as subtle thoracic size and thoracic mobility differences may be elicited by performing careful visual inspection along the line of the thorax. In a supine patient, the examiner should lower themselves to be on a level with the patient.

Tracheal deviation is an inconsistent finding. Although historic emphasis has been placed on tracheal deviation in the setting of tension pneumothorax, tracheal deviation is a relatively late finding caused by midline shift.

Abdominal distention may occur from increased pressure in the thoracic cavity producing caudal deviation of the diaphragm and from secondary pneumoperitoneum produced as air dissects across the diaphragm through the pores of Kohn.

If patients who are mechanically ventilated are difficult to ventilate during resuscitation, high peak airway pressures are clues to pneumothorax. A tension pneumothorax causes progressive difficulty with ventilation as the normal lung is compressed. On volume-control ventilation, this is indicated by marked increase in both peak and plateau pressures, with relatively preserved peak and plateau pressure difference. On pressure control ventilation, tension pneumothorax causes sudden drop in tidal volume. However, these observations are neither sensitive nor specific for making the diagnosis of pneumothorax or ruling out the possibility of pneumothorax.

The development of tension pneumothorax in patients who are ventilated will generally be of faster onset with immediate, progressive arterial and mixed venous oxyhemoglobin saturation decline and immediate decline in cardiac output. Cardiac arrest associated with asystole or pulseless electrical activity (PEA) may ultimately result. Occasionally, the tension pneumothorax may be tolerated and its diagnosis delayed for hours to days after the initial insult. The diagnosis may become evident only if the patient is receiving positive-pressure ventilation. Tension pneumothorax has been reported during surgery with both single- and double-lumen tubes.

Pneumomediastinum

As with pneumothorax, physical findings of pneumomediastinum may be variable, including absent signs in some patients. However, subcutaneous emphysema is the most consistent sign. Another sign, the Hamman sign—a precordial crunching noise synchronous with the heartbeat and often accentuated during expiration—has a variable rate of occurrence, with one series reporting 10%.

Catamenial pneumothorax

Bagan et al. point to the increase in the serum titer of the Ca125 antigen as a helpful marker of catamenial pneumothorax associated with endometriosis 74. In accordance with the presented data, the value of Ca125 that indicates high probability of endometriosis is 76 U/ml. In a study published by Haga in 2013, an increase of the Ca125 antigen to 36.7 ±42.3 U/ml was considered significant 68. However, the marker is not specific, which limits its routine use.

Pneumothorax treatment

The goal in treating a pneumothorax is to relieve the pressure on your lung, allowing it to re-expand. Depending on the cause of the pneumothorax, a second goal may be to prevent recurrences. The methods for achieving these goals depend on the severity of the lung collapse and sometimes on your overall health.

Selection among various management options in pneumothorax requires an understanding of the natural history of pneumothorax, the risk of recurrent pneumothorax, and the benefits and limitations of treatment options. Observation without oxygen, administering supplemental oxygen, simple aspiration, chest tube placement, video-assisted thoracoscopic surgery (VATS), open thoracotomy, and pleurodesis are among these options.

  • Small pneumothorax may not require treatment. If only a small portion of your lung is collapsed, your doctor may simply monitor your condition at 2-weekly intervals with a series of chest X-rays until the excess air is completely absorbed and your lung has re-expanded. Normally this takes a week or two. Supplemental oxygen may speed the absorption process.
  • Larger, and tension, pneumothorax requires aspiration of air (needle passed between the ribs, into the pleural space), with insertion of an intercostal drainage tube soon after. This drainage tube ends with an underwater seal; thus, escaping air is seen as bubbles in the water, but air from the atmosphere can not go back in.
  • Occasionally, the pneumothorax keeps bubbling after several days; this indicates the presence of bronchopleural fistula, and surgery may be needed. This involves either removal of the pleura, or adhesion of the two pleural layers to each other, by placing talc in the pleural space (talc pleurodesis).
  • A tension pneumothorax should be treated with immediate decompression with a needle in the 2nd intercostal space (between the second and third rib at the front). This is then followed by a formal intercostal tube insertion as above.
  • Treatment for catamenial pneumothorax involves hormonal therapy and surgical treatment (wedge lung resection, pleurectomy, chemical or mechanical pleurodesis, and diaphragm reconstruction – direct or using synthetic meshes) 60. Video-assisted thoracoscopic surgery (VATS) is the access of choice in the treatment of pneumothorax. Thoracotomy is indicated almost exclusively in cases of recurrence after a previous procedure. The use of video-assisted mini-thoracotomy has been suggested if the procedure involves extensive lesions within the diaphragm 62. Most authors are in agreement in their recommendations to perform bullectomy, pleurectomy, or pleurodesis.

Observation

If only a small portion of your lung is collapsed, your doctor may simply monitor your condition with a series of chest X-rays until the excess air is completely absorbed and your lung has re-expanded. This may take several weeks.

Needle aspiration or chest tube insertion

If a larger area of your lung has collapsed, it’s likely that a needle or chest tube will be used to remove the excess air.

  • Needle aspiration. A hollow needle with a small flexible tube (catheter) is inserted between the ribs into the air-filled space that’s pressing on the collapsed lung. Then the doctor removes the needle, attaches a syringe to the catheter and pulls out the excess air. The catheter may be left in for a few hours to ensure the lung is re-expanded and the pneumothorax does not recur.
  • Chest tube insertion. A flexible chest tube is inserted into the air-filled space and may be attached to a one-way valve device that continuously removes air from the chest cavity until your lung is re-expanded and healed.

Nonsurgical repair

If a chest tube doesn’t re-expand your lung, nonsurgical options to close the air leak may include:

  • Chemical pleurodesis: Using a substance (such as doxycycline or talcum powder to irritate the tissues around your lung so that they’ll stick together and seal any leaks. This can be done through the chest tube, but it may be done during surgery.
  • Drawing blood from your arm and placing it into the chest tube. The blood creates a fibrinous patch on the lung (autologous blood patch), sealing the air leak.
  • Passing a thin tube (bronchoscope) down your throat and into your lungs to look at your lungs and air passages and placing a one-way valve. The valve allows the lung to re-expand and the air leak to heal.

Surgery

Sometimes surgery may be necessary to close the air leak. In most cases, the surgery can be performed through small incisions, using a tiny fiber-optic camera and narrow, long-handled surgical tools. The surgeon will look for the leaking area or ruptured air blister and close it off.

Rarely, the surgeon will have to make a larger incision between the ribs to get better access to multiple or larger air leaks.

Ongoing care

You may need to avoid certain activities that put extra pressure on your lungs for a time after your pneumothorax heals. Examples include flying, scuba diving or playing a wind instrument. Talk to your doctor about the type and length of your activity restrictions. Keep follow-up appointments with your doctor to monitor your healing.

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