Showing posts with label pulmonology. Show all posts
Showing posts with label pulmonology. Show all posts

Apr 18, 2007

lung segment

RIGHT LUNG

Superior lobe
apical
posterior
anterior

Middle love
lateral
medial

Lower lobe
superior
anterior
medial
lateral
posterior

LEFT LUNG

Superior lobe
apical
posterior
anterior
superior
inferior

Inferior lobe
superoir
anterior basal
medial basal
lateral basal
posterior basal

Apr 16, 2007

ARDS diagnostic criteria

1. Acute onset

2. Pulmonary artery wedge pressure

3. Bilateral infiltrates on chest radiography

4. Acute respiratory distress syndrome is present if Pao2/Fio2 ratio

*Acute lung injury (ALI) is present if Pao2/Fio2 ratio is

Apr 5, 2007

Pulmonary function test

1. 폐활량 측정법(Spirometry)

  • 폐활량 및 정적 폐용적
-TV(tidal volume): 평상 호흡기량, 일회 호흡량
-RV(residual volume): 잔기량
-IRV(inspiratory reserve volume): 흡기 예비기량
-ERV(expiratory reserve volume): 호기 예비기량
-VC(vital capacity): 폐활량
-IC(inspiratory capacity): 흡기용량
-FRC(functional residual capacity): 기능성 잔기용량, chest wall의 compliance와 lung elastic recoil이 같아서 평형을 이루는 lung volume
-TLC(total lung capacity): 총폐용량
-TLC=IC +FRC=VC +RV
-RV은 spirometry만으로는 측정 불가능

  • 최대 노력성 호기곡선(maximal-effort expiratory spirogram)

a. 노력성 폐활량(forced vital capacity, FVC)
-제한성폐질환의 지표
b. 1초간 노력성 호기(forced expiratory volume at 1sec, FEV₁)
-폐쇄성폐질환의 지표
c. FEV₁/FVC
d. 노력성 호기 중간유량(forced mid-expiratory flow, FEF25~75%)
-노력성 호기량의 중간부분 50%의 평균속도(maximal mid-expiratory flow rate)
-환자의 노력과 가장 관계없는 부분
-small airway dz의 조기 진단에 민감
-정상인에서도 많은 변이성을 보이므로 재현성은 떨어짐
e. 최대 호기유속(peak expiratory flow rate, PEFP)
-곡선에서 가장 경사가 가파른 부분
-central large airway 폐쇄시 이상소견을 보임
  • 최대 환기량(maximal voluntary ventilation, MVV)-환자가 자발적인 최대 노력으로 1분간 호흡할 수 있는 기량
-호흡곤란의 정도와 상관관계가 있음
-운동능력 및 수술전후의 평가에 이용

  • 사강(dead space)
-사강=TV*(1-PeCO₂/PaCO₂)
-PaCO₂: arterial CO₂tension
-PeCO₂: mean expired CO₂tension
-정상인의 anatomical dead space 호흡량은 TV의 약 30%(1회 호흡량의 70%만 alveolar zone에 도달)
-physiologic dead space: 혈류가 흐르지 않는 폐포 공간(TV의 약 36%)

  • PFT에 의한 환기장애 분류
-폐쇄성 환기장애: FEV₁/FVC 감소, FEV₁이 주로 감소
-제한성 환기장애: FEV₁/FVC 증가, FVC가 주로 감소

  • 폐질환 분류
-obstructive: 천식, COPD, 기관지 확장증, cystic fibrosis, 세기관지염
-restrictive(parenchymal): sarcoidosis, idiopathic pulmonary fibrosis, hypersensitivity pneumonitis, pneumoconiosis, ARDS, ILD
-restrictive(extraparenchymal): neuromuscular dz(diaphragmatic weakness, MG, Guillain-Barre syndrome, cervical spine injury), chest wall dz(kyphoscoliosis, obesity, ankylosing spondylitis)

2. 유량기량 곡선(flow-volume curve)
-obstructive: 호기 시 곡선이 오목, 최대 호기유량 감소, FEF50% 크게 감소
-restrictive: 폐활량이 주로 감소하고, 유량은 별로 감소하지 않기 때문에 키가 크고 폭이 좁은 모양
-호기시 초반부 25%: 환자의 노력에 많은 영향을 받음
-호기시 후반부 75%: 환자의 노력과 관계없이 폐의 물리역학적 특성에 의해 결정(재현성 높고, 소기도의 초기 병변에 예민)
-fixed obstruction: 압력 차이에 영향을 받지 않으므로 호기와 흡기 시 모두 plateau 발생(예:tracheal stenosis, thyroid ca., bilateral vocal cord palsy)
-variable extrathoracic obstruction: 호기 시에는 내경이 확장되어 유량에 이상이 없으나, 흡기 시에는 대기압에 비해 상기도 압력이 낮아지기 때문에 상기도 내경이 좁아져서 plateau가 발생(예: croup, laryngitis, tracheal malacia, laryngeal or tracheal trauma)
-variable intrathoracic obstruction: 흡기 시에는 흉곽 내압이 음압이 되어 기도폐쇄 부위가 확장되어 유량에 이상이 없으나, 호기 시에는 반대로 plateau가 발생(예: COPD, bronchial asthma)

3. 폐용적의 측정
-RV 측정
-불활성 가스 방법
-체적변동 기록법(body plethysmography): 정확, compliance도 구할 수 있음
-면적 측정법

4. 기도저항
-생리학적인 실제 기도저항치를 측정하는 것(대개 체적변동기록법을 이용)
-R=∆P(대기압-alveolar pressure)/flow
-말초 소기도를 주로 침범하는 COPD의 초기진단에는 예민하지 못하고, 심한 만성기관지염이나 천식의 진단 및 경과 판단에 이용 가능
-임상에서 폐쇄성 폐질환의 진단 및 severity 판단은 보통 노력성 호기유량곡선을 이용

5. 폐탄성(lung compliance)
-폐의 distensibility(확장성)을 표시하는 지표로 elastic property의 기능
-정의: transpulmonary pressure 변화에 따른 폐용적의 변화
-transpulmonary pressure = alveolar pr.-pleural pr. = 구강압-식도내압

  • 정적 폐탄성(static lung compliance)
-호흡이 정지되었을 때 측정
-폐용적의 차이에 의한 변동을 없애기 위해 compliance/FRC로써 나타냄
-정적 폐탄성=TV/inspiratory plateau pr.
-증가: emphysema
-감소: 폐부종, 무기폐, 폐렴, restrictive lung dz.

  • 동적 폐탄성(dynamic lung compliance)
-동적 폐탄성=TV/(peak inspiratory pr.-PEEP)
-흡기말과 호기말의 폐용적 차이를 transpulmonary pressure로 나눈 것
-frequency dependent lung compliance또는 effective respiratory system compliance라고도 부름
-정상인에서는 호흡횟수를 증가시켜도 동일하게 유지
-기도폐쇄가 있는 경우에는 호흡횟수를 증가시킬수록 감소
-폐쇄성 폐질환의 폐에서는 폐의 균질성이 변화하여, 호흡이 빨라지면 폐의 일부분에서는 공기의 출입이 늦어져 폐용적의 변화가 적어지고 따라서 동적폐탄성이 감소됨

6. 폐쇄용적(closing volume)
-single breath N₂washout curve: RV까지 숨을 내쉰 다음, 100% O₂를 총폐용량까지 1번 흡입한 후, 서서히 숨을 내쉬면서 구강에서 N₂농도를 측정하여 그래프를 그린 것
-1단계: 상기도 내의 100% O2만 나옴
-2단계: dead space +alveolar air(서서히 N2 농도가 증가)
-3단계: 상부/하부 alveolar air가 동시에 배출되어 일정한 농도 유지
-4단계: 하부의 기도가 폐쇄(하부의 흉막강압이 상부보다 높기 때문), 상부에서만 N2 배출(고농도의 N2)
-CV: 기도폐쇄가 일어나는 폐용적(4단계의 시적점), small airway obstruction 시 CV 증가
-CV이 증가하는 경우: 폐기종, 천식, 기관지염, 흡연, 노인, CHF(평상 호흡시에도 하부기도의 폐쇄가 일어나 V/Q mismatch 초래)

  • 가스 교환의 장애
1. 정상 호흡기능을 유지하기 위한 조건
-폐포까지 신선한 공기를 적절히 공급하는 것(환기, ventilation)
-적절한 혈액의 순환(관류, perfusion)
-폐포와 모세혈관 사이에서 가스의 원활한 이동(확산, diffusion)
-폐포 가스와 모세혈관 혈액 사이의 적절한 접촉(ventilation-perfusion matching)
2. Oxyhemoglobin dissociation curve
-shift to right: 온도 증가, pH 감소, PaCO₂증가, 2,3-DPG 증가, 빈혈, 저혈압, 고지대
-shift to left: 온도 감소, pH 증가, PaCO2 감소, 2,3-DPG 감소, abnormal Hb, CO 중독
-2,3-DPG(diphosphoglycerate): O2보다 Hb에 대한 결합력이 커서 증가하면, Hb의 산소친화도를 감소시켜, O2는 Hb에서 해리되어 조직으로 공급
-Bohr's effect: PaCO₂가 증가하면 곡선이 오른쪽으로 이동
-Haldane effect: CO₂해리곡선은 HbO₂가 많이 형성될수록 오른쪽으로 이동
-혈액내에서의 O2 운반: Hb(97%), dissolved state(3%)
-혈액내에서의 CO2 운반: Hb(20~30%), HCO3(60~70%), dissolved state(7~10%)

3. Pulse oxymetry
-cutaneous arterial blood에서 산소 포화도(oxygen saturation, SaO₂)를 구함
-원리: oxygenated Hb과 total Hb를 측정하여 oxygenated Hb%을 계산
-60mmHg 이상의 PaO2에서는 PaO2의 변화를 정확히 반영하지 못함
-PaO2와 SaO2의 관계는 온도, pH, 2,3-DPG 등의 영향을 받음
-cutaneous perfusion 감소시 측정이 어렵거나 불가능할 수 있음(예: low CO, vasoconstriction)
-carboxyHb, metHb 등은 측정하지 못함

4. Alveolar ventilation
-PaCO₂가 가장 잘 반영
-PaCO₂=0.863*VCO₂/Va
-VCO₂: 분당 체내 CO₂생성량
-VA: 폐포 환기(alveolar ventilation)

5. Arterial hypoxemia의 evaluation

  • 저산소혈증의 기전
-낮은 흡입 산소 농도
-폐포 환기 저하(hypoventilation)
-단락(shunt)
-환기-관류 불균형(V/Q mismatching)
-확산장애: 대부분 V/Q mismatching을 동반

  • 감별진단
-우선 PaCO₂확인, 증가되면 hypoventilation 확인
-hypoventilation: respiratory drive 감소, NM dz
-다음 (A-a)DO₂확인
-Alveolar-arterial O₂difference=PAO₂-PaO
-PAO₂=150-1.25*PaCO₂(이상적 조건)
-(A-a)DO2=150-1.25*PaCO2-PaO2
-정상치 15mmHg 이하(30세 이하), 10년마다 3씩 증가, 노인에서는 30까지도 가능
-(A-a)DO₂증가: shunt, V/Q mismatching, diffusion 장애
-(A-a)DO₂정상: low inspired PO₂, hypoventilation(PaCO2는 증가)

  • shunt
-desaturated blood가 alveolar-capillary level에서 oxygenation되지 않고 통과하는 것(ventilation=0)
-O₂supply로 교정 안 됨!
-예: atelectasis(ARDS), intraalveolar fluid filling(ARDS, CHF, 폐렴), 선천성 심장병, pulmonary arteriovenous shunt

  • V/Q mismatch
-임상적으로 가장 흔한 hypoxia 원인
-high V/Q area(high PaO₂)에서의 혈류와 low V/Q area(low PaO₂)에서의 혈류가 합쳐져서 arterial hypoxia를 일으킴
-O₂supply로 교정됨
-예: 천식, COPD, ILD, 폐렴, pul. embolism
-apex로 갈수록 V/Q ratio 증가(ventilation에 비해 perfusion이 더 많이 하강)
-apex로부터의 혈액이 base로부터의 것보다 PO₂높고, PCO₂낮다
-저산소증이 혈관에 미치는 영향: 전신혈관은 확장, 폐혈관은 수축

6. 폐확산능(Diffusing capacity, DLCO)
-확산: 높은 농도에서 낮은 농도로 분자의 수동적 이동
-주로 0.3% CO 가스를 이용하여 측정

  • 영향을 미치는 인자
-alveolar-capillary surface area
-alveolar-capillary barrier thickness
-pul. capillary blood volume
-degree of V/Q, pulmonary edema
-hemoglobin level

  • 감소하는 경우
-ILD: alveolar-capillary unit의 scarring으로 인한 pul. capillary blood volume 및 alveolar-capillary bed area 감소에 의해)
-emphysema: alveolar wall의 파괴로 인한 surface area 감소에 의해
-pul. vascular bed의 volume 및 단면적 감소: primary pu. HTN, pul. embolism, pul. vascular dz
-membrane change: intraalveolar filling: 폐렴, 폐부종, ARDS 등
-폐절제술 후, 빈혈 등

  • 증가하는 경우
-대부분 perfusion의 증가로
-pul. capillary blood volume 증가하는 경우: CHF(초기), MS, ASD
-alveolar hemorrhage: alveolar lumen 내의 RBC에 CO가 결합(예: Goodpasture's syndrome)
-천식
-polycythemia
-운동, 비만, 임신, supine position

  • 노인에서의 폐기능 변화
-폐탄성 감소
-원통형 가슴과 동반된 흉벽 강직성의 증가
-호흡근의 약화로 인한 근력 저하
-증가: FRC, RV, (A-a)DO₂
-감소: TLC, VC, 폐확산능, FEV₁

Cor pulmonale

Clinical Manifestations

Acute RV failure causes pallor, sweating, hypotension, and a rapid pulse of small amplitude. The neck veins are distended and often exhibit prominent v waves secondary to tricuspid regurgitation. The liver may be pulsatile, distended, and tender. A systolic murmur of tricuspid regurgitation along the left sternal border may be accompanied by a presystolic (S4) gallop sound. Arterial blood gas frequently shows reduced PaO2 due to ventilation/perfusion mismatching and a low PaCO2 due to hyperventilation.

Oxygen toxicity




PEEP(Positive-end expiratory pressure)

PEEP is an adjuvunt to the mode ventilation used in cases where the FRC is reduced. At the end of expiration, the PEEP exerts pressure to oppose passive emptying of the lung and to keep the airway pressure above the atmospheric pressure. The presence of PEEP opens up collapse or unstable alveoli and increases the FRC and surface area for gas exchange, thus reducing the size of the shunt. Thus, if a large shunt is found to exist based on the estimation from 100% FiO2 (see above), then PEEP can be considered and the FiO2 can be lowered (<60%), to maintain adequate PaO2, thus reducing the risk of oxygen toxicity.

In addition to treating a shunt, PEEP is also therapeutic in decreasing the work of breathing. In pulmonary physiology, compliance is a measure of the "stiffness" of the lung and chest wall. The mathematical formula for compliance (C) = change in volume / change in pressure. Therefore, a higher compliance means that only small increases in pressure can lead to large increases in volume, which means the work of breathing is reduced. As the FRC increases with PEEP, the compliance also increases, since the partially inflated lung takes less energy to inflate further.

Indications

PEEP is a cardiodepressant and can cause severe hemodynamic consequences through decreasing venous return to the right heart and decreasing right ventricular. As such, it should be judiciously used and is indicated in two circumstances.

  • If a PaO2 of 60 mmHg cannot be achieved with a FiO2 of 60%
  • If the initial shunt estimation is greater than 25%

If used, PEEP is usually set with the minimal positive pressure to maintain an adequate PaO2 with a safe FiO2. As PEEP increase intrathoracic pressure, there can be a resulting decrease in venous return and decrease in cardiac output. A PEEP of less than 10 cmH2O is usually safe if intravascular volume depletion is absent. Older literature recommended routine placement of a Swan-Ganz catheter if the amount of PEEP used is > 10 cmH2 for hemodynamic monitoring. More recent literature has failed to find outcome benefits with routine PA catheterization when compaired to simple central venous pressure monitoring.[2] If cardiac output measurement is required, minimally invasive techniques, such as esophageal doppler monitoring or arterial waveform contour monitoring may be sufficient alternatives.[3][4] PEEP should be withdrawn from a patient until adequate PaO2 can be maintained with a FiO2 < 40%. When withdrawing, it is decreased through 1-2 cmH2O decrements while monitoring hemoglobin-oxygen saturations. Any unacceptable hemoglobin-oxygen saturation should prompt reinstitution of the last PEEP level that maintained good saturation.

Apr 4, 2007

Pleural effusion

Exudative vs Transudative

Exudative pleural effusions ≥ 1 of the following criteria

Apr 3, 2007

Drug allergy

-adverse drug reaction (ADR)
common predictable ADR(typeA) 80%
less common unpredictable ADR(typeB) 20%

-type I hypersensitivity: IgE mediated, immediate reaction
allegen과 IgE 반응하고 mast cell과 결합해 histamine 분비
histamine은 주로 vasodilation 작용
ex) anaphylaxis, atopy, asthma, urticaria, angioedema

-type II hypersensitivity: antibody-dependent cytotoxic
ex) autoimmune hemolytic anemia, 수혈거부 반응, 중증근무력증, goodpasture's syndrome

-type III hypersensitivity: immune-complex mediated
ex) serum sickness, SLE, RA, 사구체신염, 혈관염

-type IV hypersensitivity: T-cell mediated, delayed type
ex) 접촉성 피부염, 결핵, 이식거부반응, hypersensitivity pneumonitis, 갑상선염, type1-DM

-delayed reaction: 72시간 이후
-진단: History taking이 가장 중요, skin test(skin test는 type I만 detection됨, 페니실린, 세팔로스포린, 펩타이드, 인슐린, 일부 전신 마취)
prick test/intradermal test(더 많은 양):대조군(식염수)보다 2*2mm 이상

-urticaria: 24hr 지속 안됨, migration, superficial dermis
-vascularitic urticaria: 24hr 지속
-angiodema: laryngeal edema, wheezing, deep dermis & subcutaneous tissue

-fixed drug eruption
-maculopapular erythematous eruption(m/c)
-bullous eruption: 가장 심한 경우 예) erythema multiform, Steven-Johnson syndrome, overlap SJS/TEM, toxic epidermal necrolysis
-Steven-Johnson syndrome: mucosal involve, 10% 이하 벗겨짐, Bactrim, NSAIDs, acetaminophen, 7~21일 후, 약물 중단, systemic early corticosteroid(가급적 빨리), IVIG
-toxic epidermal necrolysis: 30% 이상, ICU care, 원인 약물 중단, 필요없는 약물 중단, culture, 예방적 항생제는 사용하지 않음, systemic corticosteroid 금기!, IVIG 사용!
-Acute generalized exanthematous pustulosis

-drug fever: 7~10일 이후 발생, 끊은 후 72시간 내 감소, 열이 나도 well-being sense, CRP 상승, esosinophilia, relative bradycardia

-anaphylaxis: systemic, immediate hypersensitivity reaction, skin lesion을 잘 동반, biphasic, serum tryptase, vasovagal syncope DDx(HR 측정), epinephrine 1:1000 0.1ml/kg subcutaneous injection q 20 분
-anaphylactoid reaction: Non-IgE mediated, opioids, muscle relaxant, radiocontrast agents, NSAIDs, ACEi 관련

-penicillin allergy: type I~IV 모두 가능, I이 m/c, hapten hypothesis
-semisynthetic penicillin: maculopapular rash>>anaphylaxis, skin test의 효용성 떨어짐
-penicillin allergy 있는 환자 cepha 써도 괜찮음, cepha는 skin tset 안 함

-vancomycin: red-men syndrome
-aspirin &, NSAIDs: 진단 oral provocation test

Apr 2, 2007

Tuberculosis radiology

A posterior-anterior chest X-ray is the standard view used; other views (lateral or lordotic) or CT scans may be necessary.

In active pulmonary TB, infiltrates or consolidations and/or cavities are often seen in the upper lungs with or without mediastinal or hilar lymphadenopathy. However, lesions may appear anywhere in the lungs. In HIV and other immunosuppressed persons, any abnormality may indicate TB or the chest X-ray may even appear entirely normal.

Old healed tuberculosis usually presents as pulmonary nodules in the hilar area or upper lobes, with or without fibrotic scars and volume loss. Bronchiectasis and pleural scarring may be present.

Nodules and fibrotic scars may contain slowly multiplying tubercle bacilli with the potential for future progression to active tuberculosis. Persons with these findings, if they have a positive tuberculin skin test reaction, should be considered high-priority candidates for treatment of latent infection regardless of age. Conversely, calcified nodular lesions (calcified granuloma) pose a very low risk for future progression to active tuberculosis.

Abnormalities on chest radiographs may be suggestive of, but are never diagnostic of, TB. However, chest radiographs may be used to rule out the possibility of pulmonary TB in a person who has a positive reaction to the tuberculin skin test and no symptoms of disease.

CDC guidelines for evaluation CXR

A medical examination is mandatory for all refugees coming to the U.S. and all applicants outside the U.S. applying for an immigrant visa. The purpose of the medical examination is to identify applicants with inadmissible health-related conditions such as active tuberculosis. Outside the U.S., medical examinations are performed by approximately 400 physicians (panel physicians) selected by United States Department of State consular officials. In the U.S., medical examinations are performed by approximately 3,000 physicians (civil surgeons) designated by district directors of the U.S. Citizenship and Immigration Services. Guidelines were developed by the Centers for Disease Control and Prevention (CDC).

The chest X-ray and classification worksheet is designed to group findings into categories based on their likelihood of being related to TB or non-TB conditions needing medical follow-up (either at the time of the chest X-ray or after resettlement).

Normal findings:

These are films that are completely normal, with no identifiable cardiothoracic or musculoskeletal abnormality.aa

Abnormal findings:

Chest X-Ray Findings that Can Suggest ACTIVE TB:

This category comprises all findings typically associated with active pulmonary TB. An applicant with any of the following findings must submit sputum specimens for examination. Infiltrate or consolidation—Opacification of airspaces within the lung parenchyma. Consolidation or infiltrate can be dense or patchy and might have irregular, ill-defined, or hazy borders.


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  1. Any cavitary lesion—Lucency (darkened area) within the lung parenchyma, with or without irregular margins that might be surrounded by an area of airspace consolidation or infiltrates, or by nodular or fibrotic (reticular) densities, or both. The walls surrounding the lucent area can be thick or thin. Calcification can exist around a cavity.
  2. Nodule with poorly defined margins—Round density within the lung parenchyma, also called a tuberculoma. Nodules included in this category are those with margins that are indistinct or poorly defined. The surrounding haziness can be either subtle or readily apparent and suggests coexisting airspace consolidation.
  3. Pleural effusion—Presence of a significant amount of fluid within the pleural space. This finding must be distinguished from blunting of the costophrenic angle, which may or may not represent a small amount of fluid within the pleural space (except in children when even minor blunting must be considered a finding that can suggest active TB).
  4. Hilar or mediastinal lymphadenopathy (bihilar lymphadenopathy)—Enlargement of lymph nodes in one or both hila or within the mediastinum, with or without associated atelectasis or consolidation.
  5. Linear, interstitial disease (in children only)—Prominence of linear, interstitial (septal) markings.
  6. Other—Any other finding suggestive of active TB, such as miliary TB. Miliary findings are nodules of millet size (1 to 2 millimeters) distributed throughout the parenchyma.

Chest X-Ray Findings that Can Suggest INACTIVE TB:

This category includes findings that are suggestive of prior TB, that is inactive. It must be remembered that assessments of the activity of TB cannot be made accurately on the basis of a single radiograph alone. If there is any question of active TB, sputum smears must be obtained. Furthermore, if the applicant has any signs or symptoms of TB, sputum smears must be obtained. Obtaining sputum smears is necessary if there is any question of active TB. Therefore, any applicant might have findings grouped in this category, but still have active TB as suggested by

  • The presence of signs or symptoms of TB (Class B1).
  • Sputum smears positive for AFB (Class A).
  1. Discrete fibrotic scar or linear opacity—Discrete linear or reticular densities within the lung. The edges of these densities should be distinct and there should be no suggestion of airspace opacification or haziness between or surrounding these densities. Calcification can be present within the lesion and then the lesion is called a “fibrocalcific” scar.
  2. Discrete nodule(s) without calcification—One or more nodular densities with distinct borders and without any surrounding airspace opacification. Nodules are generally round or have rounded edges. These features allow them to be distinguished from infiltrates or airspace opacities. To be included here, these nodules must be noncalcified. Nodules that are calcified are included in the category “OTHER X-ray findings, No follow-up needed”.
  3. Discrete fibrotic scar with volume loss or retraction—Discrete linear densities with reduction in the space occupied by the upper lobe. Associated signs include upward deviation of the fissure or hilum on the corresponding side with asymmetry of the volumes of the two thoracic cavities.
  4. Discrete nodule(s) with volume loss or retraction—One or more nodular densities with distinct borders and no surrounding airspace opacification with reduction in the space occupied by the upper lobe. Nodules are generally round or have rounded edges.
  5. Other—Any other finding suggestive of prior TB, such as upper lobe bronchiectasis. Bronchiectasis is bronchial dilation with bronchial wall thickening.

OTHER Chest X-Ray Findings:

Follow-up needed:

This category includes findings that suggest the need for a follow-up evaluation for non-TB conditions either at the time of the chest X-ray or after resettlement of the applicant in the United States.

  1. Musculoskeletal abnormalities—New bony fractures or radiographically apparent bony abnormalities that need follow-up.
  2. Cardiac abnormalities—Cardiac enlargement or anomalies, vascular abnormalities, or any other radiographically apparent cardiovascular abnormality of significant nature to require follow-up.
  3. Pulmonary abnormalities—Pulmonary finding of a non-TB nature, such as a mass, that needs follow-up.
  4. Other—Any other finding that the panel physician believes needs follow-up, but is not one of the above.

No follow-up needed:

This category includes findings that are minor and not suggestive of TB disease. These findings require no follow-up evaluation after resettlement of the applicant.

  1. Pleural thickening—Irregularity or abnormal prominence of the pleural margin, including apical capping (thickening of the pleura in the apical region). Pleural thickening can be calcified.
  2. Diaphragmatic tenting—A localized accentuation of the normal convexity of the hemidiaphragm as if “pulled upwards by a string.”
  3. Blunting of costophrenic angle (in adults)—Loss of sharpness of one or both costophrenic angles. Blunting can be related to a small amount of fluid in the pleural space or to pleural thickening and, by itself, is a non-specific finding (except in children, when even minor blunting may suggest active TB). In contrast a large pleural effusion, or the presence of a significant amount of fluid in the pleural space, may be a sign of active TB at any age.
  4. Solitary calcified nodules or granuloma—Discrete calcified nodule or granuloma, or calcified lymph node. The calcified nodule can be within the lung, hila, or mediastinum. The borders must be sharp, distinct, and well defined. This was considered a Class B3 TB in the past; however, Class B3 has been omitted from the classification scheme because it has not been found to be associated with active TB.
  5. Minor musculoskeletal findings—Minor findings needing no follow-up.
  6. Minor cardiac findings—Minor findings needing no follow-up.

References

External links

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