| Literature DB >> 28430880 |
Emily J Boother1,2, Sheila Brownlow3, Hannah C Tighe3, Kathleen B Bamford4, James E Jackson5, Claire L Shovlin1,3.
Abstract
Background: Cerebral abscess is a recognized complication of pulmonary arteriovenous malformations (PAVMs) that allow systemic venous blood to bypass the pulmonary capillary bed through anatomic right-to-left shunts. Broader implications and mechanisms remain poorly explored.Entities:
Keywords: hereditary hemorrhagic telangiectasia; hypoxemia; intravenous iron; oxygen; transferrin saturation index
Mesh:
Year: 2017 PMID: 28430880 PMCID: PMC5849101 DOI: 10.1093/cid/cix373
Source DB: PubMed Journal: Clin Infect Dis ISSN: 1058-4838 Impact factor: 9.079
Comparative Demographics Between Current and Previous Pulmonary Arteriovenous Malformation/Cerebral Abscess Series
| Characteristic | Current Series | Previous Seriesa | Combined |
|
|---|---|---|---|---|
| PAVM cases, No. | 445 | 219 | 664c | … |
| Date of first institutional review | June 2005–Dec 2016 | April 1984–May 2005 | … | … |
| All cerebral abscess casesd | 37 (8.3) | 28 (12.8) | 65 (9.8) | .07 |
| Male sex | 14 (38) | 17 (60.7) | 31 (47.7) | .08 |
| Abscess rate adjusting for ascertainment bias | 27/435 (6.2) | 19/210 (9.05) | 46 (7.1) | .26 |
| Age at abscess, median ( | 48 (34, 62) | 44 (32.5, 50.5) | 44 (32, 52) | .89 |
| PAVM diagnosis prior to abscesse | 8 (21.6)f | 10 (35.7) | 18 (27.7) | .27 |
| PAVM diagnosis following abscess | 29 (78.4) | 18 (64.3) | 47 (72) | .27 |
| Abscess-to-PAVM diagnosis interval, mo, median ( | 0.5 (0.4, 1.0) | 24 (0.0, 96.0) | 0.5 (0.4, 27) | .01 |
| No HHT diagnosis prior to abscess | 27 (79.4) | 17 (60.7) | 44 (70.9) | .18 |
| Permanent neurological deficit | 19 (51.4) | 17 (70.8) | 36 (55.4) | .62 |
Data are presented as No. (%) unless otherwise indicated.
Abbreviations: HHT, hereditary hemorrhagic telangiectasia; PAVM, pulmonary arteriovenous malformation.
aPreviously reported series [8].
bCategorical P values calculated by Fisher exact test, continuous values by Mann-Whitney test.
cNo individual could be in both series.
dCerebral abscess could occur at any time point until the end of the respective individual series (December 2016; May 2005) but, in the majority of cases, occurred prior to the first presentation to our institution.
eSeven had been previously treated a median of 5 years (range, 0–18 years) earlier, and 1 patient had declined treatment. Three patients experienced further abscesses (cerebral [n = 2], lung/chest [n = 2], and spinal [n = 1]).
fEight (21.6%) described respiratory symptoms (most commonly dyspnea), but these were only sufficient to precipitate PAVM diagnosis in 3 cases.
Figure 1.Persistent neurological deficits in the 37 cerebral abscess cases. Indirect neurological consequences (eg, postabscess strokes) are not included, but would increase the number of visual loss cases by 1. There were no fatalities in this group, but 3 patients with pulmonary arteriovenous malformation due to hereditary hemorrhagic telangiectasia had first-degree relatives who died as a direct result of a cerebral abscess. “?” represents cases where the final neurological outcome was not yet known.
Bacterial Species Cultured From the Pulmonary Arteriovenous Malformation Patients With Cerebral Abscesses
| Species | Current Cohort | Previous Cohort [9]a | Total Isolates | |||
|---|---|---|---|---|---|---|
| Cases | Associationsb | Cases | Associations | Cases | % of 24 Positive Isolates | |
| Streptococcal spp | 4 | 3/4 dental | 5 | 4/5 dental | 9 | 41 |
| | 1 | Scale and polish, poor dental hygienec | 3 | Post scale and polish (2 cases) | 4 | 18d |
| | 1 | Ongoing major dental work | 1 | Very poor dental hygiene | 2 | 9 |
| Nonhemolytic streptococci | 1 | Deep gum pocket periodontitis | … | … | 1 | 5 |
| α-Hemolytic streptococci | 1 | None recorded | … | … | 1 | 5 |
| Uncharacterized | … | … | 1 | Very poor dental hygiene | 1 | 5 |
|
| 2 | Extraction, poor dental hygiene | 2 | Dental platesf | 4 | 18 |
|
| 1 | Recent dental work | … | … | 1 | 5 |
| Unspecified anaerobe species | 1 | Scale and polish, poor dental hygienec | … | … | 1 | 5 |
| Bacteroides spp | … | … | 2 | Dental platesf | 2 | 9 |
|
| … | … | 1 | Dental platesf | 1 | 5 |
|
| … | … | 1 | Dental work and fillings | 1 | 5 |
| MRSA, | … | … | 1 | Recent venous access | 1 | 5 |
| Uncharacterized gram-positive rods | … | … | 2 | Poor dentition, dental abscess | 2 | 9 |
| Uncharacterized gram-positive cocci | … | … | 1 | Dental abscess | 1 | 5 |
Abbreviation: MRSA, methicillin-resistant Staphylococcus aureus.
aMicrobiological isolates include those from 4 additional abscesses in the previous cohort [8] that occurred after study closure, and thus were not included in either abscess series.
bAll evident at the time or recalled within 12 months of intervention.
cSame case.
dNote that in 118 pediatric cases presenting to 4 UK neurosurgical centers over 12 years, this was the most frequent organism (38% of positive cultures), except after penetrating head injury or neurosurgery, for which Staphylococcus aureus was most common [30].
e Actinomyces israelii, Actinomyces meyeri, and unspecified.
fSame case.
Timing of Interventional and Dental Histories for the 37 Patients With Cerebral Abscess
| Event/State | No. of Cases (2005–2016 Series) | Range of Timepoints (Months Previously) |
|---|---|---|
| Dental infections | 3 | |
| Dental abscess(es) | 3 | Ongoing |
| Deep gum pocket periodontitis | 1 | Ongoing |
| Dental interventiona | 11 | |
| Scale and polish | 4 | 0.5–3 (mean, 1.6) |
| Dental extraction | 2 | 6–12 (mean, 9) |
| Root canal treatment | 1 | 5 |
| Occlusive braces | 1 | Ongoing ≥12 mo, poor hygiene |
| Other dental work | 3 | Ongoing, 0.25 mo and “recent” |
| Bronchoscopy | 1 | 1 |
| Obstetric surgeryb and epidural | 1 | 1 |
| Intravenous access | 3 | ≥1 wk |
aSeven individuals in dental intervention groups were also recorded on clinical examination at the time, or within 1 year, to have poor or very poor dental hygiene. Only 1 of the patients with a known diagnosis of pulmonary arteriovenous malformation used prophylactic antibiotics as recommended [8, 22].
bCesarean delivery.
Evaluations at Assessment Closest to Abscess
| Variable | No. | (%) | No. | (%) |
| ||
|---|---|---|---|---|---|---|---|
| Binary variables | |||||||
| Sex (female = 1) | 19 | (51.3) | 248 | (60.1) | .26 | ||
| Cerebral abscess | 37 | (100) | 0 | (0) | |||
| Clinical ischemic stroke | 3 | (8.1) | 55 | (13.4) | .41 | ||
| Migraine | 11 | (29.7) | 112 | (27.5) | .51 | ||
| Multiple PAVMs | 28 | (75.7) | 213 | (52.2) | .016 | ||
| Definite HHT | 34 | (91.9) | 368 | (90.2) | .62 | ||
| Use of oral iron | 10 | (27) | 109 | (26.7) | .63 | ||
| Use of intravenous iron | 4 | (10.8) | 14 | (3.4) | .018 | ||
| Use of blood transfusions | 4 | (10.8) | 23 | (5.6) | .16 | ||
| Cerebral hemorrhage | 0 | (0) | 3 | (0.73) | .6 | ||
| Liver transplantation for hepatic AVM | 0 | (0) | 1 | (0.25) | .76 | ||
| Smoking history | 8 | (21.6) | 92 | (22.5) | .98 | ||
| High blood pressure | 5 | (13.5) | 39 | (9.56) | .39 | ||
| Venous thromboemboli | 4 | (10.8) | 14 | (3.43) | .022 | ||
| Diabetes mellitus | 1 | (2.7) | 9 | (2.2) | .86 | ||
| Continuous variables | No. | Median (Q1, Q3) | Range | No. | Median (Q1, Q3) | Range | |
| Age, y | 37 | 50 (36, 62) | 19–76 | 408 | 48 (34, 62) | 16–89 | .6 |
| Oxygen saturation at abscess, % | 34 | 92.1 (89, 95) | 74–98 | 398 | 95.0 (91.8, 96.3) | 72–99 | .0016 |
| Hemoglobin, g/L | 35 | 144 (127, 158) | 74–203 | 391 | 140 (125, 155) | 59–201 | .39 |
| Arterial oxygen content, mL/dL | 34 | 17.9 (13.8, 19.2) | 9.4–21.3 | 385 | 17.5 (15.9, 19.2) | 7.6–24.3 | .75 |
| Platelet count, ×109/dL | 34 | 252 (208, 295) | 138–502 | 371 | 261 (221, 307) | 70–606 | .38 |
| Platelet volume, fL | 32 | 10.9 (10.3, 11.4) | 9.5–13 | 367 | 10.6 (10, 11.2) | 4.3–13.8 | .04 |
| Prothrombin time, sec | 32 | 11.0 (10.6, 11.4) | 9.9–22.8 | 367 | 10.7 (10.4, 11.2) | 9–38.1 | .037 |
| Activated partial thromboplastin time, sec | 32 | 26.3 (25.5, 28.3) | 19.3–36.5 | 365 | 26.2 (24.7, 28.1) | 13.2–43 | .53 |
| Fibrinogen, g/L | 32 | 3.1 (2.47, 3.59) | 1.47–4.65 | 361 | 3.03 (2.56, 3.58) | 1.55–7.16 | .8 |
| C-reactive protein, IU/mL | 30 | 2 (1.4, 4) | 0.2,21 | 354 | 2.0 (1.2, 3.8) | 0–118.2 | .66 |
| Serum iron, umol/L | 33 | 15 (8, 22) | 2.0–277.0 | 366 | 14 (8, 19) | 0–64 | .25 |
| Transferrin saturation index, % | 33 | 27 (13, 36) | 0–100 | 365 | 21 (11, 29) | 0–89 | .18 |
| Ferritin, μg/L | 31 | 34 (20, 83) | 3–151 | 342 | 34 (15, 73) | 0–1795 | .55 |
| Largest PAVM feeding artery diameter, mm | 25 | 5 (4, 6) | 1–10 | 307 | 5 (2, 6) | 0–14 | .58 |
| Pulmonary artery pressure, mean, mm Hg | 25 | 13 (12, 16) | 5–28 | 213 | 14 (12, 16) | 6–50 | .51 |
Range of interval to abscess: 9 months preabscess to 480 months postabscess (median, 9 months [interquartile range, 4–9 months] postabscess). Use of presentation data did not materially affect the respective ranks or P values (Supplementary Table 2).
Abbreviations: AVM, arteriovenous malformation; HHT, hereditary hemorrhagic telangiectasia; PAVM, pulmonary arteriovenous malformation.
Multiple Logistic Regression Analyses of Cerebral Abscess Risk
| Risk Factor | Odds Ratio | 95% Confidence Interval |
|
|---|---|---|---|
| Oxygen saturation | 0.895 | .836–.958 | .001 |
| Male sex | 2.625 | 1.18–5.86 | .019 |
| Transferrin saturation index | 1.026 | 1.002–1.049 | .034 |
| Intravenous iron | 5.423 | 1.397–21.06 | .015 |
| Venous thromboemboli | 3.848 | 1.012–14.63 | .048 |
This model of 380 individuals explained 12.2% of the variance of cerebral abscess (P = .0001). The model, and the preceding univariate analyses, were robust to the exclusion of the tiniest pulmonary arteriovenous malformations that may have been overreported on computed tomography (Supplementary Table 3), and to the inclusion or exclusion of venous thromboemboli (deep venous thromboses and/or pulmonary emboli; data not shown).
Figure 2.Comparison of the cerebral abscess risk receiver operating characteristic (ROC) model from oxygen saturation (SaO2) alone (dotted line/open symbols) and final model with SaO2, sex, transferrin saturation index, intravenous iron, and venous thromboembolus (solid black line/symbols). The 2 models provide areas under the curve of 0.63 and 0.73, respectively (P = .0012). Inclusion of feeding artery diameter marginally reduced the strength of the models, and the association was negative, implying that cerebral abscess were marginally more common for pulmonary arteriovenous malformations with smaller feeding artery diameters, once adjusted for other components of the model.
Figure 3.Variation of parameters across the transferrin saturation index (TfSI) quartiles. A, TfSI (%), where the normal institutional range was 20%–40%. Note that because boundary values were allocated to a single quartile, the exact numbers across Q1–Q4 were 89, 103, 105, and 101, respectively. B, Percentage of patients with cerebral abscess. C, Oxygen saturation (SaO2) where normal is ≥96%. D, Gender (% male). In all graphs, bars indicate mean and standard error of the mean. Across Q1–Q4, intravenous iron rates were 7.9%, 1.9%, 2.9%, and 5.0%, and venous thromboembolus rates were 3.4%, 7.8%, 5.7%, and 1.0%, respectively.