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Age and Ageing Advance Access originally published online on June 11, 2008
Age and Ageing 2008 37(6):710-713; doi:10.1093/ageing/afn127
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© The Author 2008. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Bronchoscopy in octogenarians

SIR—Fiberoptic bronchoscopy (FOB) is an important diagnostic and therapeutic tool and is considered to be a safe procedure [1]. Factors that may increase the risk of FOB include the general condition of the patient, the specific procedure performed, available facilities, skills and experience of the medical personnel [1–5]. The reported frequency of complications associated with FOB varies between 0.3 and 30% [1–5], however, the definition of complications varies between studies.

There is a high prevalence of respiratory diseases in the elderly, and FOB is often indicated in these patients. Only a few studies evaluating FOB in the elderly have been reported [6–13]. Most of these studies conclude that elderly patients tolerate bronchoscopy as well as younger patients and that FOB is safe and has a high diagnostic yield. However, these studies include only a small number of patients over 80 years of age.

In the present study, we evaluate the safety, diagnostic and therapeutic yield of FOB in patients aged 80 years and older, and compare these with procedures performed in younger patients.

Methods

Two thousand nine hundred and sixty-nine FOBs were performed in adult patients at Hadassah Medical Centre between January 1997 and April 2004. The patients included both outpatients and inpatients including those on mechanical ventilation. One hundred and seventy three FOBs were performed on 150 patients 80 years or older (octogenarians). This group constituted the study population. The control group comprised 201 FOBs randomly chosen from the 2,796 procedures performed on patients aged 19–79 years (the computerised randomisation was arbitrary, using patient identification numbers). A retrospective analysis was done in both groups to evaluate the indications; type of procedure, diagnostic and therapeutic yield and rate of complications (during bronchoscopy and up to 24 h after the procedure). The mortality rate was calculated from all the 2,969 bronchoscopies done during these years.

All FOBs were performed by a certified pulmonary physician or a pulmonary fellow under the guidance of a pulmonary physician with the assistance of a specialist bronchoscopy nurse. Nasal anaesthesia was administered using 2% topical lidocaine jelly. Vocal cord and airway anaesthesia was administered using 2–4% lidocaine administered through the bronchoscope. Conscious sedation was achieved with midazolam with occasional addition of pethidine. All patients received supplemental oxygen and were monitored with pulse oximetry, a 3-lead electrocardiogram and intermittent non-invasive blood pressure measurements. Patients on mechanical ventilation received 100% oxygen during the procedure and were sedated with midazolam or propofol. Bronchoalveolar lavage was performed by installation of 2–3 doses of 60 ml aliquots of 0.9% saline through the bronchoscope to a specific lung segment. Transbronchial biopsies (TBB) were performed using fluoroscopy guidance. Following bronchoscopy, patients were monitored for complications for 3–6 h. Routine chest X-ray was performed in all patients who underwent TBB.

Patient details were obtained by reviewing medical files and bronchoscopy reports. The information included patient gender, age, past medical history, concomitant illnesses, medications, indications for the bronchoscopy, where the bronchoscopy was performed (bronchial suite, intensive care unit), premedication used, type of procedure performed (bronchoalveolar lavage, biopsies etc.), findings with bronchoscopy, complications, diagnostic and therapeutic yield and final diagnosis. Complications were defined by the pulmonologist responsible for the procedure during the bronchoscopy, or shortly after the bronchoscopy. Chi-square analysis was performed to identify differences between the groups.

Results

Patients
One hundred and seventy three FOBs were performed in 150 patients 80 years of age or older. Mean patient age was 84.9 ± 3.3 years (range 80–101 years). Ninety-eight procedures were done in men (57%) and 75 in women (43%). The mean age in the control group was 53.2 ± 14.6 years. The proportion between the genders was similar—59% in men and 41% in women (Table 1). We found no differences between the groups in the prevalence of ischaemic heart disease, diabetes mellitus, hypertension, malignancy or chronic lung disease. The study group included one immunosuppressed patient and the control group included 19 immunosuppressed patients (P < 0.05).


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Table 1. Patient groups and final diagnosis

 
Indications and procedures
The most frequent indications for bronchoscopy in both groups were suspected infection and suspected tumour. The number of bronchoscopies done on patients on mechanical ventilation was higher in the octogenarian group (35%), compared to the control group (25%) (P = 0.03). The rate of endobronchial biopsy was similar between the groups –29% in octogenarians and 27% in the control group. TBB was performed in 18% of the octogenarians as compared to 30% in the control group (P = 0.006).

Diagnosis
The final diagnoses in octogenarians were similar to that found in the control group (Table 1). The diagnostic yield of bronchoscopy was 63% in octogenarians and 52% in the control group (P = 0.04). The combination of diagnostic and therapeutic benefit was 88% in the octogenarians and 87% in the control group.

Complications
The frequency of complications and the mortality rate were significantly higher in octogenarians (Table 2). Twenty patients had 26 complications in the octogenarian group compared to 11 patients and 13 complications in the control group (11.5% versus 5.5% P = 0.04). The difference is even more significant considering the lower rate of TBBs performed in octogenarians and the difference in immunosuppressed patients. Complications included hypoxaemia (deterioration of saturation below 90%), bleeding, pneumothorax, arrhythmia, hypotension, bronchospasm, stridor and fever. Frequency of bleeding was similar in the two groups (4% versus 3.5% in controls), but the rate of other complications was higher in octogenarians as compared to the control group. The main difference was in hypoxaemia –6.3% in octogenarians and 1.5% in the control group (P = 0.03, Table 2). The mortality rate was calculated from all the bronchoscopies done during these years. Two patients in the octogenarian group died (1.2%). The death rate in patients aged 18–79 years was 1/2,796 (0.035%). The difference reached statistical significance (P = 0.001). The young patient and one of the old patients who died were on mechanical ventilation at the time of bronchoscopy.


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Table 2. Complications and mortality (values are percentages)

 
Discussion

In this retrospective study, we evaluated the use of FOB in patients 80 years of age and older. To our knowledge, this is the largest cohort of patients reported in this age group. Our study also included patients on mechanical ventilation (35% in the octogenarian group and 25% in the control group). The large number of patients on mechanical ventilation relates to the fact that the study was performed in a tertiary centre. Indications for FOB, diagnostic and therapeutic yields and the final diagnosis in octogenarians were similar to those observed in younger patients. These findings are comparable to those observed in previous studies done on elderly patients [6–13].

In our study, the frequency of complications (11.5%) and mortality rate (1.2%) were significantly higher in octogenarians as compared to the control group. This is in contrast to the study of Allan and Ouellette who reported a complication rate of only 3.3% (similar to those in younger patients) with no deaths among 120 bronchoscopies performed in octogenarians [12].

The difference between this study and our study may be related to the different cohort of patients; Allan's study included army veterans, with a mean age of 82.8 years, and they excluded patients on mechanical ventilation. In our study, patients were slightly older (84.9 ± 3.3 years) and included a high percentage of patients on mechanical ventilation. However, we found no difference in the frequency of complications between ventilated and non-ventilated patients.

In the study of Hehn et al., the authors reviewed 1,359 FOB of which only 30 procedures were performed on patients 80 years of age or older [13]. They found a 33% incidence of adverse events, which was significantly higher than that observed in younger patients (10%). As in our study, they found that hypoxaemia was the most frequent adverse event in octogenarians (13.3%). The rate of complications in this study was higher than in our study (33% compared to 11.5%), and in all likelihood, this difference relates to differences in definitions of complications. The authors conclude that there is an increased risk for adverse events with increasing age; most of the complications are minor, suggesting that chronological age should not be a contraindication for bronchoscopy in older patients.

In our study, we also found that most of the complications were minor, however, we cannot discount the higher complication rate and mortality observed in octogenarians in a procedure considered to be very safe. Nevertheless, the difference is even more significant considering the lower rate of TBBs performed in octogenarians, and the lower rate of immunosuppressed patients among octogenarians. It is possible that the main factor accounting for the difference in complications is the severity of coexistent illness in octogenarians rather than age per se. Our study was performed retrospectively, and we could not, therefore, evaluate the severity of the diseases. Two of the three deaths were in ventilated patients. It is possible that the basic critical situation contributed to the death, rather than age per se. A large prospective study is needed to confirm our findings.

Key points

  • In octogenarians, indications for FOB, final diagnosis, diagnostic yield and therapeutic benefit were similar to that observed in younger patients.
  • Bronchoscopy in octogenarians provides a high diagnostic and therapeutic benefit, but is associated with a higher morbidity rate than that observed in younger patients.

Funding

This work received no financial support.

Conflict of interest

The authors have no conflict of interest regarding this work.

Acknowledgements

This study was carried out at the Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

Ariel Rokach1,*, Zvi G. Fridlender1, Nissim Arish2 and Neville Berkman1

1 Institute of Pulmonology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
2 Department of Medicine C, Hadassah-Hebrew University Medical Center, Jerusalem, Israel

* To whom correspondence should be addressed Email: rokach.ariel{at}gmail.com

References

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  2. Bulpa PA, Dive AM, Mertens L, et al. Combined bronchoalveolar lavage and transbronchial lung biopsy: safety and yield in ventilated patients. Eur Respir J (2003) 21:489–94.[Abstract/Free Full Text]
  3. Prakash UBS, Offord KP, Stubbs SE. Bronchoscopy in North America: the ACCP survey. Chest (1991) 100:1668–75.[CrossRef][Web of Science][Medline]
  4. Cordasco EM, Jr, Mehta AC, Ahmad M. Bronchoscopically induced bleeding: a summary of nine years' Cleveland Clinic experience and review of the literature. Chest (1991) 100:1141.[CrossRef][Web of Science][Medline]
  5. Sang WU, Chang MC, Choon TL, et al. Prospective analysis of clinical characteristics and risk factors of postbronchoscopy fever. Chest (2004) 25:945–52.
  6. Macfarlane JT, Storr A, Wart MJ, et al. Safety, usefulness and acceptability of fiberoptic bronchoscopy in the elderly. Age Ageing (1981) 10:127–31.[Abstract/Free Full Text]
  7. Brandstetter RB, Croce SA, Schiaffino E, et al. Flexible fiberoptic bronchoscopy in the elderly. N Y State J Med (1984) 84:546–8.[Web of Science][Medline]
  8. O'hickey S, Hilton AM. Fibreoptic bronchoscopy in the elderly. Age Ageing (1987) 16:229–33.[Abstract/Free Full Text]
  9. Knox AJ, Mascie-Taylor BH, Page RL. Fiberoptic bronchoscopy in the elderly: 4 years' experience. Br J Dis Chest (1988) 82:290–3.[CrossRef][Web of Science][Medline]
  10. Costello RW, O'Donnel D, Collins D, et al. The elderly tolerate fiberoptic bronchoscopy as well as younger patients. J Bronchol (1997) 4:115–9.
  11. Hehn BT, Haponik EF. Flexible bronchoscopy in the elderly. Clin Chest Med (2001) 22:301–9.[CrossRef][Web of Science][Medline]
  12. Allan PF, Quellette D. Bronchoscopic procedure in octogenarians. J Bronchol (2003) 10:112–7.[CrossRef]
  13. Hehn BT, Haponik EF, Rubin HR, et al. The relationship between age and process of care and patients tolerance of bronchoscopy. J Am Geriatr Soc (2003) 51:917–22.[CrossRef][Web of Science][Medline]

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