Pulmonary Pathologic Findings of Fatal 2009 Pandemic Influenza A/H1N1 Viral Infections

Abstract

Context

In March 2009, a novel swine-origin influenza A/H1N1 virus was identified. After global spread, the World Health Organization in June declared the first influenza pandemic in 41 years.

Objective

To describe the clinicopathologic characteristics of 34 people who died following confirmed A/H1N1 infection with emphasis on the pulmonary pathology findings.

Design

We reviewed medical records, autopsy reports, microbiologic studies, and microscopic slides of 34 people who died between May 15 and July 9, 2009, and were investigated either by the New York City Office of Chief Medical Examiner (32 deaths) or through the consultation service of a coauthor (2 deaths).

Results

Most of the 34 decedents (62%) were between 25 and 49 years old (median, 41.5 years). Tracheitis, bronchiolitis, and diffuse alveolar damage were noted in most cases. Influenza viral antigen was observed most commonly in the epithelium of the tracheobronchial tree but also in alveolar epithelial cells and macrophages. Most cases were reverse transcription–polymerase chain reaction positive for influenza. Histologic and microbiologic autopsy evidence of bacterial pneumonia was detected in 55% of cases. Underlying medical conditions including cardiorespiratory diseases and immunosuppression were present in 91% of cases. Obesity (body mass index, >30) was noted in 72% of adult and adolescent cases.

Conclusions

The pulmonary pathologic findings in fatal disease caused by the novel pandemic influenza virus are similar to findings identified in past pandemics. Superimposed bacterial infections of the respiratory tract were common. Preexisting obesity, cardiorespiratory diseases, and other comorbidities also were prominent findings among the decedents.

Influenza A viruses are important causes of respiratory disease in pandemic form and in annual seasonal influenza. At least 36 000 people die annually of influenza complications in the United States.¹ Pandemic influenza emerges sporadically and may differ dramatically in impact.^2,3 The 1918 pandemic killed approximately 675 000 people in the United States and at least 40 million people worldwide.^4,5 Pandemics in 1957 and 1968 were significantly less severe.²

In March 2009, a novel influenza A virus of H1N1 subtype was identified from patients in Mexico and the United States. The virus was a novel genetic reassortant derived from 2 preexisting swine influenza virus lineages. ⁶ During the spring, the outbreak spread throughout the United States and globally. In June, the World Health Organization declared the first influenza pandemic in 41 years.⁷ As of November 8, 2009, the World Health Organization had reported more than 503 536 confirmed H1N1 infections and at least 6260 deaths, although the case total is undoubtedly larger⁸ and is rising as the pandemic continues to spread globally.

Whereas in seasonal influenza most deaths occur in persons older than 65 years,⁹ the 2009 pandemic has predominantly affected the young, with a median age between 12 and 22 years.^10–12 Most infections have been self-limited, but deaths have also occurred in a younger age group than expected for seasonal influenza (median age, 37 years).¹³ In a subset of fatal cases for which medical records were available, 91% had preexisting underlying medical conditions, notably cardiac and respiratory diseases, immunosuppression, pregnancy, and obesity, the latter being an unexpected finding based on evidence from prior pandemics.¹³

We investigated 34 deaths with confirmed novel A/H1N1 respiratory infection, reviewing available clinical, radiologic, pathologic, and microbiologic data.

MATERIALS AND METHODS

Patients

In May 2009, the New York City Office of Chief Medical Examiner began investigating all suspected influenza deaths, including all unexplained deaths involving febrile respiratory illnesses and all sudden pediatric deaths with or without a history of febrile illness. Of the 42 confirmed New York City A/H1N1 deaths investigated by the New York City Office of Chief Medical Examiner between May 15, 2009, and July 9, 2009, 32 underwent autopsy examination that included gross, microscopic, microbiologic, and toxicologic study. At family request, 10 additional cases were externally examined with nasopharyngeal swabs obtained for viral testing. In addition, 2 deaths from other jurisdictions (Washington State and Long Island, New York) were seen in consultation by one of us (W.D.T.).

Pathologic and Microbiologic Studies

Histologic examination included routine hematoxylin-eosin staining on formalin-fixed, paraffin-embedded (FFPE) respiratory tract sections. Sections from 33 of 34 fatal cases were examined for fungi using Gomori methenamine silver stain and for bacteria using Brown and Hopps tissue Gram stain.

Further microbiologic investigation included swabs of the nasopharynx and trachea in all autopsied cases with suspected or known A/H1N1 infection. Viral studies were performed by the Centers for Disease Control and Prevention and the New York City Public Health Laboratory. Novel A/H1N1 viral RNA was detected by real-time reverse transcription–polymerase chain reaction.¹⁴ Real-time reverse transcription–polymerase chain reaction was also performed on FFPE autopsy tissue sections¹⁵ for the influenza A virus matrix gene^16,17 and novel A/H1N1 hemagglutinin gene.¹⁸ Immunohistochemical studies for influenza A viral antigen were performed following antigen retrieval.¹⁹

RESULTS

Study Patients

Age and gender data (Table 1 and Table 2) indicate that 62% of patients were 25 to 49 years old; fatal cases included 2 previously healthy infants (ages 2 and 4 months) and 1 person older than 60 years.

Table 1.

Characteristics of the 34 Study Decedents Who Had Confirmed Infection With Novel Influenza A/H1N1 Virus and Underwent Autopsy

Characteristic	Value
Female sex, No./Total No. (%)	17/34 (50)
Age, median (range), y	41.5 (0.16–72)
Age, y, No./Total No. (%)
≤5 y	2/34 (6)
>5 to ≤10 y	0/34 (0)
>10 to ≤15 y	1/34 (3)
>15 to ≤50 y	21/34 (62)
>50 to ≤60 y	9/34 (26)
>60 y	1/34 (3)
Symptom, No./Total No. (%)
Fever (temperature >38°C)	30/32 (94)
Cough	31/34 (91)
Dyspnea or respiratory distress	24/33 (73)
Mechanical ventilation on admission	12/21 (57)
Rhinorrhea	15/26 (58)
Myalgia/arthralgia	12/24 (50)
Clinical evidence of sepsis	8/17 (47)
Gastrointestinal symptoms	11/28 (39)
Hypotension that did not resolve after       fluid administration	6/18 (33)
Wheezing	3/21 (14)
Hemoptysis	2/28 (7)
Body mass index, mean, median (range)	39.9, 37.5 (21–70)
Known in 27 deaths: time from onset of     symptoms to death, median (range), d	7 (2–44)
Known in 16 deaths: time from onset of     symptoms to emergency room, median     (range),ad	6 (1–7)
Known in 22 deaths: time from admission     to death, median (range),a d	7 (0.4–40)

^aThirteen of 34 decedents were pronounced dead on arrival at the hospital or scene of death.

Table 2.

Pulmonary Pathology Microscopic and Microbiologic Findings of the 34 Study Decedents Who Had Confirmed Infection With Novel Influenza A/H1N1 Virus and Underwent Autopsy

Case No.	Age/Sex	Underlying Medical Conditions	Length of Hospitalization	Major Histopathologic Findings	Bacteriologic Resultsa	Gram Stainb	Influenza IHCc	Influenza PCRd
1	55 y/F	Down syndrome,     cirrhosis	36 h	Acute bacterial pneumonia,     focal acute DAD,     tracheitis, bronchitis	Streptococcus     pneumoniae	+++	+	+
2	41 y/F	Asthma, HTN,      DM, obesity	DOA	Asthmatic bronchitis	−	−	+ (trachea)	+ (trachea)
3	2 mo/M	None	DOA	Cellular interstitial     pneumonia, focal acute     bacterial pneumonia,     focal acute bronchiolitis	S pneumoniae	+	+	+
4	43 y/F	Asthma, COPD,     IVDA	16 h	Extensive necrotizing     bacterial pneumonia,     focal acute DAD	MRSA	+++	+	+
5	72 y/F	AIDS (most     recent CD4,     290/mm3),     HTN, CAD,     substance     abuse, home     oxygen     therapy	24 h	Acute and chronic     bronchiolitis	−	−	+	+
6	53 y/M	CHF with AICD,     HTN, DM	17 h	Tracheitis and asthmatic     bronchitis, changes     consistent with CHF	−	−	+	+
7	30 y/M	HTN, obesity,     DM	40 d	Focal acute bacterial     pneumonia, pulmonary     edema	S pneumoniae	+	−	−
8	34 y/M	Asthma, obesity	DOA	Focal acute and organizing     bacterial pneumonia,     focal DAD, asthmatic     bronchitis	S pneumoniae	+	+	+
9	47 y/F	Obesity	DOA	Marked acute DAD with     marked hyaline     membranes, focal acute     pneumonia	−	+++	+	+
10	38 y/F	Obesity with     sleep apnea	2 d	Acute DAD, acute     necrotizing bacterial     pneumonia	−	+	+	+
11	11 y/F	Obesity	DOA	Acute DAD with marked     hyaline membranes,     acute bacterial     pneumonia, acute and     chronic bronchiolitis	S pneumoniae and     Streptococcus     pyogenes (GAS)	++	−	−
12	46 y/M	Obesity, HTN	DOA	Acute DAD with focal     hyaline membranes,     extensive pulmonary     edema, acute pneumonia,     focal mild chronic     bronchiolitis	−	−	+	+
13	31 y/M	Obesity	7 d	Acute DAD, acute     necrotizing pneumonia	−	−	+	−
14	47 y/F	HTN, CAD,     IVDA	9 h	Acute DAD with focal     hyaline membranes,     extensive pulmonary     edema, focal acute     bacterial pneumonia	S pyogenes     (GAS)	+++	+	−
15	54 y/F	Multiple     myeloma,     status post     stem cell     transplant,     obesity, HTN	16 d	Acute DAD with marked     hyaline membranes,     acute infarct and     thromboemboli	−	−	+	+
16	58 y/F	HTN,     emphysema,     psoriasis on     infliximab     (Remicade)	DOA	Acute DAD with marked     hyaline membranes,     ulcerative laryngitis	NT	++	+	+
17	32 y/M	ESRD, DM,     HTN, CAD	DOA	Mild bronchitis and     bronchiolitis	−	NT	+ (trachea)	−
18	49 y/F	HTN, HIV,     asthma,     COPD, DM	6 d	Acute DAD with marked     hyaline membranes, focal     acute bacterial     pneumonia	−	+	+	+
19	56 y/F	HTN, obesity	DOA	Acute necrotizing bacterial     pneumonia, pulmonary     edema, bronchitis and     bronchiolitis	S pyogenes     (GAS)	++	+	+
20	25 y/F	39 weeks     pregnancy,     HTN,     preeclampsia	18 d	Acute and organizing DAD,     acute necrotizing     bacterial pneumonia	−	+	+	−
21	31 y/M	Slightly obese     (autopsy BMI,     35)	9 d	Acute and organizing DAD,     acute infarct and     thromboemboli, focal     acute pneumonia	−	−	+	+
22	51 y/F	AIDS, IVDA,     MDS	30 d	Acute and organizing DAD     with marked hyaline     membranes, acute infarct     and thromboemboli, focal     acute pneumonia	−	−	−	−
23	55 y/F	Asthma, IVDA	13 d	Acute and organizing DAD     with marked hyaline     membranes, asthmatic     tracheitis and bronchitis	−	+	+	−
24	55 y/M	HTN, CAD,     obesity	4 d	Focal acute DAD	−	−	+	−
25	4 mo/M	None	DOA	Chronic bronchitis and     bronchiolitis	−	−	+	+
26	59 y/F	HTN, CAD	10 d	Acute and organizing DAD	−	−	+	+
27	28 y/M	Obesity, asthma	DOA	Acute bacterial pneumonia	S pneumoniae	+++	+	+
28	44 y/F	HTN	DOA	Acute and organizing DAD	S pneumoniae	++	+	−
29	35 y/F	Obesity	4 d	Acute DAD with marked     hyaline membranes	−	+	+	+
30	35 y/F	Obesity, sleep     apnea, asthma,     HTN	2 d	Acute and organizing DAD     with marked hyaline     membranes	−	−	+	+
31	27 y/M	No known risk     factors	25 d	Fibrosing and organizing     DAD, focal acute     bacterial pneumonia	−	++	+	−
32	37 y/M	AML	14 d	Acute DAD with marked     hyaline membranes, AML	NT	−	+	+
33	39 y/M	Obesity,     hypertrophic     cardio-     myopathy	DOA	Acute DAD, changes     consistent with CHF	NT	−	+	+
34	42 y/F	Overweight	38 d	Fibrosing and organizing     DAD, focal acute and     chronic pneumonia	NT	−	+	+

Abbreviations: −, negative; AICD, automatic implantable cardioverter defibrillator; AML, acute myelogenous leukemia; BMI, body mass index; CAD, coronary artery disease; CHF, congestive heart failure; COPD, chronic obstructive pulmonary disease; DAD, diffuse alveolar damage; DM, diabetes mellitus; DOA, dead on arrival; ESRD, end-stage renal disease; GAS, Group A streptococci; HIV, human immunodeficiency virus; HTN, hypertension; IHC, immunohistochemistry; IVDA, intravenous drug abuse; MDS, myelodysplastic syndrome; MRSA, methicillin-resistant Staphylococcus aureus; NT, not tested; PCR, polymerase chain reaction.

^aPostmortem bacteriologic results listed include culture, immunohistochemistry, and/or PCR. Lung tissue from 30 of 34 fatal cases was examined by immunohistochemistry for specific bacterial antigens (Streptococcus pneumoniae, Streptococcus pyogenes, Staphylococcus aureus, and Haemophilus influenzae)²¹,²² at the Centers for Disease Control and Prevention’s Infectious Diseases Pathology Branch.

^bTissue Gram stain results listed as +++, numerous Gram-positive bacteria present; ++, Gram-positive bacteria present; +, rare Gram-positive bacteria present; NT, not tested.

^cInfluenza immunohistochemistry was performed using a polyclonal anti-nucleoprotein antibody as previously described¹⁹ and was scored as either positive (+) or negative (−); (trachea), positive only in trachea not in lung sections.

^dReverse transcriptase–polymerase chain reaction for influenza viral RNA was performed from RNA extracted from the formalin-fixed paraffin-embedded autopsy tissue blocks using primer sets for the influenza A virus matrix gene and specific primer sets for the pandemic H1N1 virus, scored as positive (+) or negative (−); (trachea), positive only in trachea not in lung sections.

Pulmonary Pathologic Findings

A spectrum of histopathologic changes was observed in both the upper and lower respiratory tissues (Figure 1; Table 2 and Table 3). Tracheitis and bronchitis of focal or extensive nature were observed in all cases (Figure 1, A through E and H), typically consisting of denuded or ulcerated epithelial layers, focal squamous metaplasia, and submucosal inflammatory infiltrates. Moderate to marked inflammation of the submucosal glands and ducts with focal epithelial cytonecrosis was typical (Figure 1, A). Focal mild to moderate bronchiolitis (Figure 1, J) was observed in 18 of 34 cases, sometimes associated with squamous metaplasia. Influenza viral pneumonia with focal to extensive diffuse alveolar damage (DAD) was seen in 25 of 34 cases (Figure 1, I), often associated with marked hyaline membrane formation, pulmonary edema, and, in 8 of 34 cases, acute pulmonary hemorrhage. Sixteen of these 25 DAD cases showed only acute DAD (average time in hospital, 3.4 days). Seven of 25 cases showed acute and organizing DAD (average time in hospital, 11.7 days). Two of 25 cases had fibrosing and organizing DAD (average time in hospital, 31.5 days). Thrombotic changes similar to changes observed in 1918²⁰ were seen in 9 of 34 cases. Autopsy evidence of acute pneumonias, ranging from focal to extensive in distribution, were observed in 19 of 34 cases (Figure 1, F), usually in association with bacteria (Figure 1, G; see Autopsy evidence of acute bacterial pneumonia and detection of bacteria).

Figure 1.

Representative histopathologic changes associated with fatal pandemic influenza A/H1N1 infection. Photomicrographs of hematoxylineosin–stained tissue sections and immunohistochemically stained sections to detect influenza viral antigen are shown. A, Acute necrotizing tracheitis and inflammation of the submucosal tracheal mucus glands (case 2) (hematoxylin-eosin, original magnification ×400). B and C, Immunohistochemical stain for influenza in a section of trachea. Viral antigen is stained red-brown on a hematoxylin-stained background. Arrow shows influenza antigen–positive cells in the submucosal gland. Arrowhead shows influenza antigen–positive cells in the tracheal epithelium. Section stained with anti-influenza primary antibody in B and without the primary antibody in C demonstrating specific staining (case 15) (original magnifications ×100 [B and C]). D and E, Immunohistochemical staining for influenza in a section of trachea. Viral antigen is stained red-brown on a hematoxylin-stained background. Arrows show influenza antigen-positive cells in acinar cells of a submucosal gland (D) and in ductal mucus cells, including basal cells (E) (case 17) (original magnifications ×1000 [D and E]). F, Section of lung showing a massive infiltration of neutrophils in the airspaces of alveoli associated with bacterial bronchopneumonia (case 19) (hematoxylin-eosin, original magnification ×100). G, Brown and Hopps modified tissue Gram stain showing chains of bacteria (arrow) morphologically compatible with streptococci (case 19) (original magnification ×1000). H, Immunohistochemical staining for influenza in a section of bronchus. Viral antigen is stained red-brown on a hematoxylin-stained background. Arrow shows influenza antigen–positive cells in the bronchial epithelium. Section shows an acute necrotizing bronchitis with transmural infiltration of inflammatory cells (case 25) (original magnification ×100). I, Section of lung showing diffuse alveolar damage with hyaline membranes lining an alveolar duct and adjacent alveoli (arrow). The alveolar air spaces contain edema fluid, strands of fibrin, desquamated epithelial cells, and inflammatory cells (case 10) (hematoxylin-eosin, original magnification ×100). J, Immunohistochemical staining for influenza in a bronchiole. Viral antigen is stained red-brown on a hematoxylin-stained background. Influenza antigen–positive cells are seen in the bronchiolar epithelium, including ciliated cells (arrowhead), and in the nuclei of some basilar cells (arrow) (case 25) (original magnification ×400). K through M, Immunohistochemical staining for influenza in alveolar cells. Viral antigen is stained red-brown on a hematoxylin-stained background. Influenza antigen–positive cells (arrows) include lveolar macrophages (K; case 1) and alveolar epithelial cells, both type I (L; case 15) and type II (M; case 24). The cytoplasm of the alveolar macrophages shown in K also contains bacteria morphologically compatible with Streptococcus pneumoniae (arrowhead) (original magnifications ×1000 [K, L, and M]).

Table 3.

Major Pulmonary Autopsy Diagnoses of the 34 Study Decedents Who Had Confirmed Infection With Novel Influenza A/H1N1 Virus and Underwent Autopsy

Characteristic	No./Total No. (%)
Lung Weightsa
Right, mean (range), g	1100 (500–1690)
Left, mean (range), g	910 (250–1510)
Tracheitis	17/17 (100)
Bronchitis	20/20 (100)
Bronchiolitis	18/23 (78)
Diffuse alveolar damage	25/34 (74)
Autopsy evidence of acute pneumonia	19/34 (56)
Pulmonary thrombosis	9/34 (27)
Alveolar hemorrhage	8/34 (24)
Chronic interstitial inflammation	4/34 (12)
Other underlying pathology
Histologic evidence of asthma	3/34 (9)
Histologic evidence of heart failure	2/34 (6)
Leukemic infiltrates	1/34 (3)
Evidence of bacterial coinfection by tissue
Gram stain	18/33 (55)
Bacterial coinfection among decedents with     acute pneumonia tested for bacteria by     culture, immunohistochemistry, and/or     PCR	10/30 (33)

Abbreviation: PCR, polymerase chain reaction.

^aInfant lung weights excluded (51 g, 43 g and 76 g, 55 g).

Influenza Viral Detection

Novel A/H1N1 virus was detected antemortem or at autopsy in all 34 decedents, including by real-time reverse transcription–polymerase chain reaction on postmortem nasopharyngeal and/or tracheal swab samples in 28 (82%) and by real-time reverse-transcription polymerase chain reaction on FFPE lung and/or tracheal tissues in 23 of 34 cases (68%; Table 2). The longest interval in which viral RNA was detected after the onset of respiratory symptoms was 12 days for postmortem nasopharyngeal samples and 38 days for FFPE material. The 6 decedents in which viral RNA was not detected in nasopharyngeal samples had intervals between 17 and 44 days; all had received oseltamivir phosphate (Tamiflu) while hospitalized, and 5 of the 6 had antemortem detection of H1N1 viral RNA. H1N1 RNA was subsequently detected by real-time reverse transcription-polymerase chain reaction from FFPE lung in the sixth decedent. Twelve of 18 inpatients were treated with oseltamivir phosphate and 4 other outpatients received prescriptions. Two outpatient prescriptions were not filled.

Immunohistochemistry for influenza viral antigen revealed prominent staining in the pseudostratified columnar epithelium of the tracheobronchial tree (Figure 1, B and H) and its associated submucosal glands (Figure 1, D and E). Focal viral antigen positivity in bronchiolar epithelium was seen (Figure 1, J). Viral antigen was seen commonly in alveolar macrophages but was seen less frequently in alveolar type I and type II cells (Figure 1, K through M). Viral antigen was often detected both in the cytoplasm and in the nuclei of alveolar macrophages, suggesting viral replication in macrophages. Antigen-positive alveolar macrophages containing visible cytoplasmic bacteria were also observed (Figure 1, K).

Autopsy Evidence of Acute Bacterial Pneumonia and Detection of Bacteria

Autopsy evidence of acute pneumonia was seen in 19 of 34 cases (56%) and was necrotizing/extensive in 5 cases (15%). Thirty-three of 34 cases were examined for evidence of pulmonary bacterial infection by tissue Gram stain. Of these, 18 (55%) showed bacterial pneumonia, 16 being morphologically compatible with streptococci and 2 with staphylococci. Of the 30 cases evaluated by postmortem bacteriologic culture and immunohistochemistry, 10 (4 of whom had been hospitalized before death) had evidence of bacterial infection: 6 with Streptococcus pneumoniae, 2 with Streptococcus pyogenes, 1 with S pneumoniae and S pyogenes, and 1 with methicillin-resistant Staphylococcus aureus (Table 2 and Table 3).^21,22 Most of these bacterial-positive cases (15 of 18; 83%) also had histologic evidence of acute pneumonia, consistent with the high percentage of secondary bacterial pneumonia described in fatal cases from earlier pandemics.^23–25 The remaining 3 had acute and organizing DAD with chronic inflammatory cells and bronchiolitis.

Radiographic Findings

Chest radiographs demonstrated features ranging from patchy opacities to areas of confluent density (not shown), corresponding with radiologic pulmonary features characterized in greater detail on computed tomography (CT) (Figure 2, A through D). On CT, the lungs of all 4 patients displayed patchy ground-glass opacities, in which underlying parenchymal architecture remained visible with discernible bronchovascular margins in a predominantly peripheral and peribronchial distribution, consistent with DAD. One case (Figure 2, D) also showed areas of denser consolidation obscuring underlying parenchymal architecture and bronchovascular margins, consistent with a secondary bacterial pneumonia identified at autopsy.

Figure 2.

Chest computed tomography examinations. The lungs of all 4 patients show rounded patches of ground-glass peribronchial opacity (yellow arrows) in a peripheral distribution. In A (case 24), the opacities are discrete and multifocal, while in B (case 26) they are confluent in subpleural areas, and in C (case 21) the entire right lung displays confluent ground-glass attenuation. These changes may correspond to areas of diffuse alveolar damage seen on histopathologic examination (see text). In addition to patchy ground-glass opacities, D (case 1) shows areas of denser consolidation in the right upper lobe and the superior segment of the right lower lobe (blue arrows) that are consistent with the bacterial pneumonia diagnosed in this patient.

Risk Factors and Comorbidities

Of the 20 New York City deaths following hospital admission, 6 occurred in municipal hospitals and 14 in private hospitals. Twelve of these 20 patients presented in advanced respiratory distress requiring mechanical ventilation on admission. Ten (29%) had outpatient visits prior to death or subsequent hospitalization. Gastrointestinal symptoms, including nausea, vomiting, diarrhea, and/or abdominal pain, were described in the medical records of 11 of 28 decedents.

Causes of death, risk factors for death, and comorbidities are summarized in Table 4. Obesity, heart disease, and underlying pulmonary disease were most common. One A/H1N1-positive patient’s death (case 6) was certified as a complication of hypertensive and atherosclerotic cardiovascular disease and of diabetes mellitus. Despite histologic evidence of tracheitis and bronchiolitis, A/H1N1 infection was not included as a cause of death in this patient. The 1 patient in the series older than 60 years (case 5) also had AIDS.

Table 4.

Cause of Death and Contributing Conditions of the 34 Study Decedents Who Had Confirmed Infection With Novel Influenza A/H1N1 Virus and Underwent Autopsy

Characteristic	No./Total No. (%)
Proximate cause of death
Novel influenza A (H1N1) viral respiratory       infection	24/34 (70)
Novel influenza A (H1N1) viral respiratory       with immunocompromised state (ie,       acute myelocytic leukemia, AIDS,       myeloma with therapy, immunotherapy       for psoriasis)	5/34 (15)
Novel influenza A (H1N1) viral respiratory       infection complicating bronchial asthma	2/34 (6)
Diabetes mellitus with end-stage renal       disease with novel influenza A (H1N1)       viral respiratory infection as a       contributing condition	1/34 (3)
Hypertensive cardiovascular disease with       novel influenza A (H1N1)
Viral respiratory infection as a       contributing condition	1/34 (3)
Hypertensive and atherosclerotic       cardiovascular disease	1/34 (3)
Comorbidities/contributing conditions/risk factors
Body mass index, mean, median (range)a	39.9, 37.5 (21–70)
Obesitya	23/32 (72)
Body mass index ≤30	9/32 (28)
Body mass index >30 to ≤39 (obesity)	8/32 (25)
Body mass index >39 (extreme obesity)	15/32 (47)
Obesity as sole risk factora	5/32 (16)
Heart disease (atherosclerotic,       hypertensive, cardiomyopathy)	17/34 (50)
Chronic obstructive pulmonary disease/       asthma	8/34 (24)
Diabetes mellitus	3/34 (9)
Infants	2/34 (6)
Pregnancy	1/16 (6)
End-stage kidney disease (diabetes mellitus)	1/34 (3)
Chronic substance abuse	1/34 (3)
Cirrhosis (chronic hepatitis B)	1/34 (3)
Immunocompromise
HIV positive (with AIDS)	3/34 [2/34] (9)
Multiple myeloma with chemotherapy       and stem cell transplant	1/34 (3)
Immunotherapy for psoriasis	1/34 (3)
Acute myelocytic leukemia	1/34 (3)
Total decedents with one or more       comorbidity or risk factora	29/32 (91)

Abbreviation: HIV, human immunodeficiency virus.

^aThe two infants were excluded.

Seventy-two percent of the adult and adolescent decedents were obese (body mass index [BMI] ≥30)²⁶ (Table 4). The single adolescent death in the series had a BMI of 34. Among the 11 adults who were dead on arrival (and therefore received no fluid resuscitation), the median BMI was 47 (range, 25–62). A pregnant woman, who presented at 39 weeks’ gestation with fever, cough, obesity, and preeclampsia, died of A/H1N1 respiratory complications following an emergent Cesarean section.

Two adult decedents without significant underlying illnesses were slightly obese. One (case 21) had a BMI of 35 following 9 days of hospitalization with significant fluid overload at autopsy. The second (case 34) had a BMI of 38 at autopsy but had been admitted to hospital 38 days earlier with a BMI of 27 and subsequently developed marked anasarca. One decedent (case 31) had no known comorbidities. Overall, 29 of 32 adult decedents (91%) had underlying risk factors (Table 2 and Table 4).

COMMENT

The decision by the New York City Office of Chief Medical Examiner to investigate deaths associated with infection by the 2009 pandemic influenza virus provides an opportunity to examine the pathogenesis of fatal pandemic influenza. Major findings include (1) tracheitis and/or bronchitis in all cases, with DAD-associated viral pneumonia as the primary pathology; (2) distribution of influenza viral antigen predominantly in the tracheobronchial epithelium and submucosal glands, and to a lesser extent in bronchiolar epithelium and alveolar epithelial cells and macrophages; (3) bacterial pneumonia in 55%; and (4) comorbidities in 91% of adult and adolescent decedents (with obesity in 72%). These pathologic findings are strikingly similar to those of published autopsy studies from the 1918 and 1957 pandemics and to a more limited extent from publications investigating seasonal influenza.^23,25,27,28

Although pandemic and seasonal influenza generally cause self-limited illnesses, a small percentage of cases are fatal.²⁵ In typical uncomplicated infections, viral replication apparently remains limited to the mucosal lining of the pharynx and upper tracheobronchial tree. Determinants of progression of a predominantly upper respiratory tract infection to fatal pulmonary disease are poorly understood but likely include a number of different factors such as age, immune and underlying health status, preexisting immunity to viral antigens (principally hemagglutinin), ²⁹ and pharyngeal bacterial flora. The findings in this and other studies²⁴ suggest that severe disease is associated with the development of influenza viral pneumonia,^23,25,30 with or without secondary bacterial pneumonia.^24,31,32

The pulmonary pathologic abnormalities observed in the 2009 fatalities reported here do not differ significantly from those reported by pathologists who performed meticulous autopsies during the 1918 and 1957 pandemics (reviewed in references 23 and 25). For example, influenza viral antigen in the tracheobronchial epithelium, alveolar lining cells, and alveolar macrophages, as shown here by immunohistochemistry (Figure 1), was first demonstrated by immunofluorescence in 1957 pandemic autopsy cases.²³ Our observation that viral antigen in alveolar cells often did not colocalize with foci of DAD and alveolar hyaline membrane formation likely reflects the rapid asynchronous kinetics of influenza viral replication and clearance.²⁵ It could also be consistent with recent speculation that at least some of the pulmonary abnormalities of fatal influenza viral pneumonia might be induced by the release of host inflammatory mediators, rather than by a direct viral cytopathic effect.^33,34 Whether such pulmonary pathologic changes might also occur in patients with self-limited influenza infection is not known.

Bacterial pneumonia was observed in 55% of the fatalities described here. In comparison, postmortem cultures for bacteria were positive in more than 90% of 1918 pandemic autopsies and about 75% of 1957 autopsies. ^23,25 Of the 13 decedents who died without having been hospitalized, 8 (62%) had evidence of bacterial pneumonia (Table 2), suggesting that community acquired bacterial pneumonia may play a significant role in the current pandemic. In addition, 8 of these 13 decedents also had DAD, confirming that these changes are not just secondary to prolonged mechanical respirator support but a component of the viral disease process as described in the 1918 and 1957 pandemics. Nine decedents had pulmonary thrombi including 5 with focal infarcts. Thrombi are common with DAD and have been described with influenza infection since 1918.^20,35 One of the 2 infant deaths (case 3) also had bacterial pneumonia. A recent report by the Centers for Disease Control and Prevention described concurrent bacterial infection in 29% of referral specimens from influenza A/H1N1 fatalities.²¹ As this report notes, inadequate sampling, collection of specimens from unaffected portions of the lung, or prolonged illness or treatment may limit the detection of bacteria and explain the variations in percentages of detection.²¹ Regardless, these findings suggest that, even in an era of widespread and early antibiotic use, bacterial pneumonia remains an important factor in severe/fatal influenza. In coming months it will be important for clinicians to diagnose and treat bacterial pneumonias occurring in patients infected with the pandemic influenza virus. Unfortunately, there is insufficient clinical information about the natural history of severe influenza disease to fully inform clinicians about optimal prophylaxis and treatment approaches.

In addition to demonstrating the characteristics and constancy of pulmonary abnormalities in fatal pandemic influenza, this case series emphasizes an association between underlying illnesses and mortality. Epidemiologic studies conducted during the current pandemic^13,35 have suggested obesity as an important risk factor for fatal outcomes. Nearly half of the patients in this case series had a BMI greater than 40. Enhanced susceptibility to fatal infection in obese persons might reflect associated independent risk factors such as compromised ventilatory function, hypertension, congestive heart failure, or diabetes mellitus.³⁶ The presence of only a single decedent older than 60 years is also consistent with current reports that older individuals are less vulnerable to infection with the 2009 A/H1N1 virus than with seasonal influenza viruses, presumably because of immunologic protection induced by prior exposure to previously circulating human A/H1N1 viruses.³⁷ It is not yet clear whether the comparatively few fatalities in older persons is due entirely to low incidence of infection by itself, or whether there may be lower case fatality as well. The frequent gastrointestinal symptomatology (39%) in these patients is an area that needs further study with respect to the underlying pathology of the gastrointestinal tract.

A potentially important diagnostic modality in the new influenza pandemic is CT imaging, which provided detailed information on antemortem pathologic changes in the lungs of 4 patients in this case series. Our findings suggest that CT can be a valuable tool in identifying patients who will require intensive medical support and to elucidate the pathogenesis of severe disease. At present we do not know to what extent the CT abnormalities seen in these fatal cases also occur in patients with milder infections, but this question, as well as differentiating viral from bacterial infections, can be investigated in clinical trials, in volunteer challenge studies, and with quantitative CT analysis.

Pandemic progression offers an opportunity to study pandemic influenza viral infection using techniques not available in past pandemics, including enhanced surveillance, rapid genetic analyses, improved radiographic imaging techniques, and better tools to evaluate the immune response and the natural history of uncomplicated and severe disease. A better understanding of secondary bacterial pneumonias will be crucial for the treatment of severely ill influenza patients. Our findings suggest that, although the spectrum of pulmonary pathologic abnormalities has remained similar from pandemic to pandemic during the past 120 years,²⁴ the portion of the human population that is most susceptible to lethal infection differs with each new viral emergence, confirming the continuing importance of epidemiologic studies identifying risk groups and the continuing importance of careful autopsy pathology studies and the value of centralized evaluation of deaths by a medical examiner’s office.