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Abstract

Background:

Free tissue transfer reconstruction carries significant complication rates in surgical head and neck oncology. A registry-based approach offers a possibility to investigate the factors affecting increased morbidity and early mortality, that is, death within 6 months of treatment.

Methods:

A retrospective registry review was conducted on a series of 317 consecutive microvascular free tissue transfers in head and neck cancer patients performed during 2013–2017 at the Helsinki University Hospital (Helsinki, Finland). All surviving patients had a minimum follow-up of 2 years (range 24–84 months).

Results:

Overall, 36 (11.4%) early deaths occurred in this series. In multivariable logistic regression analysis, patients aged 75 years and older (p = 0.019), Adult Comorbidity Evaluation-27 (ACE-27) score of 3 (p = 0.048), tumor class T3 (p = 0.005), lymph node class N2 (p = 0.014), or thrombocyte count of 360 (× 10⁹ L) or more (p = 0.001) were more likely to die within 6 months of surgery. Of these 36 patients, 27 (75%) had a complication warranting hospital care and most (n = 22, 61%) had several complications.

Conclusions:

Early postoperative mortality most frequently affects patients aged 75 years and above, with a high ACE-27 score, advanced tumor stage, or high thrombocyte count. Therefore, preoperative assessment and patient selection should have a crucial role in this patient population.

Keywords

Head and neck cancer early mortality head and neck surgery microvascular free flap postoperative complication

Context and Relevance

The purpose of the study is to determine the value-based treatment of head and neck cancer patients. Value-based care includes the quality of care, for example, complications and the results, for example, survival. We investigated the factors affecting early mortality, that is, death within 6 months of treatment. A retrospective registry review was conducted on a series of 317 consecutive microvascular free tissue transfers in head and neck cancer patients performed during 2013–2017 at the Helsinki University Hospital (Helsinki, Finland). Early postoperative mortality most frequently affects patients aged 75 years and above, with a high ACE-27 score, advanced tumor stage, or high thrombocyte count. Therefore, preoperative assessment and patient selection should have a crucial role in this patient population.

Introduction

Head and neck cancer (HNC) is the seventh most common cancer in the world.¹ Management consists of either surgery or (chemo)radiotherapy, or their combination.² Reconstruction of tissue defects with microvascular free flaps has become the standard of surgical HNC care.^3–5

The frequency of postoperative complications after head and neck free tissue reconstructions varies considerably (20%–72%) between published reports.^6‑10 Severe postoperative complications clearly decrease overall survival.¹¹ A specialty-specific surgical risk calculator was created to predict postoperative complications and to facilitate surgical decision-making.¹² Nevertheless, the risk calculator is not adaptable to patients with head and neck microvascular free flap reconstruction due to the nature of the surgery and the associated complications.¹³ Therefore, further investigations are needed to identify patients with an increased risk for postoperative complications and early death. These risk factors can be used to optimize treatment and preoperative decision-making.

Early mortality, that is, death within 6 months of diagnosis, is an important phenomenon among HNC patients and can be either cancer-, patient- or treatment-related.¹⁴ Talani et al.¹⁵ reported an early-death rate of 4.5% for patients with curative intent of treatment in a series of 8751 HNC patients in the Swedish HNC Quality Registry. The identified risk factors in their study were older age, advanced stage, hypopharyngeal site, and higher WHO score. Mortality associated with HNC reconstructive free flap surgery has not been studied extensively.^16–19 A recent systematic literature review found that, on average, 1.2% of these patients will die less than 30 days after free flap reconstruction.²⁰ While the identification of reasons for early death is crucial to guide treatment decisions in this patient population, the literature on these aspects is limited. L’Esperance et al.²¹ examined 3-month mortality in a series of patients aged 80 years and older undergoing ablative head and neck oncologic surgical procedures and found a mortality rate of 10.4%. Lahtinen et al.,²² the only study reporting on 6-month mortality, examined a series of 146 HNC patients, with only 10 deaths occurring during the first 6 months of follow-up after microvascular reconstruction.

The aim of this study was to find the risk factors for early death after HNC surgery with primary microvascular free flap reconstruction. We applied a registry-based approach to identify and investigate a real-world series of patients at an academic tertiary care center.

Methods

The present non-selective series was identified in the hospital registry at the Helsinki University Hospital (HUS) (Helsinki, Finland) and comprised all patients undergoing a primary free tissue transfer reconstruction for HNC ablative surgery between 2013 and 2017. An electronic search for these patients was conducted by the Department of Data Management using HNC diagnoses (International Classification of Diseases 10th revision (ICD-10) classification) and surgical procedure codes (Nordic Medico-Statistical Committee (NOMESCO) Classification of Surgical Procedures).

Between 2013 and 2017, 1784 new patients with HNC were treated at HUS. After excluding patients who were not treated with curative intent, did not undergo free tissue transfer reconstruction, or had had prior (chemo)radiotherapy or oncologic head and neck surgery, 317 patients were included in the study. Patient-related factors are presented in Supplemental Table 2. Median age was 65 (range 21–94) years and the majority (n = 191, 60.3%) were male. All patients had a minimum follow-up time of 2 years (range 24–84 months). Early mortality was defined as death within 6 months of surgical treatment.

Department of Data Management collected the data which included the following: demographics (age, gender, body mass index (BMI), American Society of Anesthesiologists (ASA) Physical Status Classification, Nutritional Risk Screening 2002 (NRS2002), preoperative laboratory values—hemoglobin (Hb), leukocytes (Leuc), thrombocytes (Thromb), C-reactive protein (CRP), creatinine (Crea), sodium (Na), and albumin (Alb)), percutaneous endoscopic gastrostomy (PEG), tracheostomy, length of intensive care, length of hospital stay, hospital death, death within 6 months of surgery, and death later than 6 months after surgery. In addition to using registry data, a retrospective analysis of medical records was performed. We collected and completed data which included pre-existing medical conditions, usage of corticosteroids and anticoagulants, smoking, and alcohol usage. Tumor-related factors were tumor location and tumor, nodes, and metastases (TNM) classification.Treatment- and follow-up-related factors comprised intent of treatment (curative or palliative), operative technique, postoperative chemoradiotherapy, postoperative complications, and persistent growth of tumor.

The Charlson Comorbidity Index (CCI), age-adjusted Charlson Comorbidity Index (ACCI), and Adult Comorbidity Evaluation-27 (ACE-27) score were calculated as indicators of comorbidity. Two clinicians (anesthesiologist and otorhinolaryngologist) graded all complications using the Clavien–Dindo classification system.²³ Causes of death were provided by Statistics Finland, and the underlying cause of death was used in the analysis.

Descriptive statistics are presented as means or medians with ranges for continuous variables and numbers with percentages for categorical variables. Mean age between groups was compared using one-way analysis of variance with Tukey’s method in pairwise comparisons and median BMI values using Kruskal–Wallis test with Dunn–Bonferroni method in pairwise comparisons. Chi-square test was used to test the difference in patient characteristics (categorical variables) between groups. The associations of risk factors with early death were analyzed using binary logistic regression. Risk factors significantly associated with early mortality (death within 6 months of treatment versus alive at 6 months) in univariate analysis were entered in multivariable logistic regression model. Backward selection (exclusion criteria p ⩾ 0.05) was used to select the significant risk factors for the final multivariable model. As an additional analysis, the associations of risk factors for death within or after 6 months of surgical treatment compared to surviving until the end of follow-up were examined using multinomial logistic regression. Alive at the end of the follow-up was used as a reference category in multinomial logistic regression. Results of logistic regression models are expressed using odds ratios (OR) with 95% confidence intervals (CI). Survival curve was estimated with Kaplan–Meier method. Statistical analyses were performed using IBM SPSS Statistics 27 for Windows (IBM Corp., Armonk, NY). The p-values less than 0.05 were considered as statistically significant.

Study permission was granted by the Research Administration of the Helsinki and Uusimaa Hospital District (HUS/419/2018). Research Ethics Board approval for the retrospective registry study was not needed in accordance with Finnish legislation.

Results

Risk factors for early death

In 317 patients, a total of 113 patients died during the follow-up period of this study. Most of these deaths (n = 83, 73.5%) occurred within 2 years of surgery (Fig. 1). Overall, 36 patients (11.4%) died within 6 months of the primary surgery. However, 4 out of these 36 (11.1%) died before their planned postoperative treatment commenced. Those patients who died within 6 months of surgery had a higher mean age (70.1 versus 64.2 years, p = 0.005), lower median BMI (22.6 versus 24.7, p = 0.013), and higher ASA, CCI, ACCI, and ACE-27 scores compared to patients who were alive 6 months after treatment (p < 0.001 for all) (Table 1). There were no differences in smoking and alcohol use between those who died within 6 months and those who were alive at 6 months.

Fig. 1.

The survival rate of 317 head and neck cancer patients undergoing microvascular reconstruction with free flap tissue transfer during 2013–2017.

Table 1.

Patient characteristics of 317 patients undergoing free flap reconstruction after surgery for head and neck cancer during 2013–2017.

Demographics	Died within 6 months of surgery (n = 36)	Alive at 6 months after surgery (n = 281)	p value
Age, mean (range)	70.1 (33–94)	64.2 (21–94)	0.005
Male, n (%)	24 (66.7)	167 (59.4)	0.404
BMI, median (range)	22.6 (12.3–35.1)	24.7 (16.2–48.5)	0.013
History of smoking, n (%)			0.421
Current	20 (55.6)	130 (46.3)
Former	5 (13.9)	33 (11.7)
Non-smoker	11 (30.6)	118 (42.0)
Alcohol misuse, n (%)	12 (33.3)	79 (28.1)	0.515
ASA class, n (%)			<0.001
1–2	3 (8.3)	103 (36.7)
3	17 (47.2)	138 (49.1)
4	16 (44.4)	40 (14.2)
CCI score, n (%)			<0.001
0	12 (33.3)	166 (59.1)
1–2	14 (38.9)	91 (32.4)
⩾3	10 (27.8)	24 (8.5)
ACCI score, n (%)			<0.001
0	0 (0)	22 (7.8)
1–2	9 (25.0)	121 (43.1)
3–4	11 (30.6)	99 (35.2)
⩾5	16 (44.4)	39 (13.9)
ACE-27 score, n (%)			<0.001
0	5 (13.9)	76 (27.0)
1	7 (19.4)	116 (41.3)
2	5 (13.9)	55 (19.6)
3	19 (52.8)	34 (12.1)
Immunosuppressive medication, n (%)	5 (13.9)	18 (6.4)	0.160
Anticoagulant use, n (%)	7 (19.4)	30 (10.7)	0.162
Preoperative laboratory values, median (range)
Hemoglobin (g/L)	130 (95–177)	136 (82–177)	0.031
Leucocytes (× 10⁹ L)	8.5 (3.1–24.2)	7.6 (3.5–24.7)	0.167
Thrombocytes (× 10⁹ L)	296 (172–734)	255 (96–683)	0.011
C-reactive protein (mg/L)	13 (0–218)	0 (0–224)	<0.001
Creatinine (µmol/L)	68 (31–154)	70 (38–184)	1.000
Sodium (mmol/L)	138 (126–145)	139 (123–153)	0.075
Albumin (g/L)	34 (27–42)	39 (20–46)	<0.001

ACCI: age-adjusted Charlson Comorbidity Index; ACE-27: Adult Comorbidity Evaluation 27; ASA: American Society of Anesthesiologists; BMI: body mass index; CCI: Charlson Comorbidity Index.

Results for univariable binary logistic regression are shown in Supplemental Table 1. Multivariable binary logistic regression analyses showed that the preoperative factors contributing significantly to early death after HNC microvascular free flap reconstruction were age 75 years or older, ACE-27 score of 3, elevated thrombocytes, T3 tumor stage, and N2 lymph node stage. Multivariable analyses showed that postoperative factors significantly associating with early death were tracheostomy and length of hospital stay of 20 days or more (Table 2).

Table 2.

The associations of factors with early death (within 6 months of treatment) by multivariable binary logistic regression analysis.

Factors	Adjusted OR (95% CI)^a	p value
Age
<60	1
⩾60–64	2.70 (0.47–15.49)	0.265
65–69	0.38 (0.44–3.30)	0.382
70–74	3.42 (0.47–24.61)	0.223
⩾75	7.64 (1.40–41.64)	0.019
ACE-27 score
0	1
1	1.75 (0.34–9.10)	0.505
2	0.72 (0.12–4.50)	0.725
3	5.55 (1.01–30.38)	0.048
Thrombocyte (× 10⁹ L)
<360	1
⩾360	9.20 (2.60–32.58)	0.001
T stage
T1–T2	1
T3	24.41 (2.58–231.31)	0.005
T4	1.53 (0.44–5.36)	0.507
N stage
N0	1
N1	0.14 (0.01–1.91)	0.138
N2	5.78 (1.43–23.36)	0.014
Tracheostomy
No	1
Yes	9.26 (1.76–48.74)	0.009
LOS (days)
<10	4.74 (0.75–30.08)	0.099
10–19	1
⩾20	7.03 (1.81–27.35)	0.005
Oncological treatment
Follow-up or death before
Oncological treatment	10.80 (2.11–55.31)	0.004
Radiotherapy	1
Chemoradiotherapy	0.69 (0.11–4.48)	0.701

ACE: adult comorbidity evaluation; CI: confidence interval; LOS: length of stay; N: lymph node; OR: odds ratio; T: tumor.

Adjusted for other variables included in the model.

Risk factors for overall mortality

We analyzed the pre- and postoperative risk factors for patients who died either within or after 6 months during the follow-up and for patients who were alive at the end of follow-up. Median follow-up time was 4.24 years for all surviving patients (range 24–84 months). Those patients who died within 6 months of surgery had a higher mean age (70.1 versus 63.9 years, p = 0.011), lower median BMI (22.6 versus 24.9, p = 0.015), and higher ASA, CCI, ACCI, and ACE-27 scores compared to surviving patients (p < 0.001 for all) (Supplemental Table 2). There were no differences in smoking and alcohol use between those who died within 6 months and those who survived. However, when comparing those who died more than 6 months after treatment and those surviving until the end of the follow-up period, there was a statistical significance regarding both smoking (p = 0.009) and alcohol misuse (p < 0.001). Multivariable multinomial logistic regression analysis showed that the risk factors for early death compared to surviving until the end of the follow-up period were the same as in binary logistic regression listed above, excluding age and ACE-27 score. In addition, surgical complications and hospital stay of less than 10 days were significant risk factors for early death (Table 3). Nonetheless, of those who had a hospital stay of less than 10 days, three out of six died in the hospital less than 10 days postoperatively, two were transferred to their local secondary hospital, and one was well enough to be discharged directly to home, which would explain this finding and the wide confidence interval (OR = 10.04, 95% CI: 1.53–65.79, p = 0.016). ASA class of 3 and 4, CCI score of 3 or more, misuse of alcohol, and medical complications were significant risk factors for death later than 6 months after surgery compared to surviving until the end of the follow-up period.

Table 3.

The associations of factors with early death (within 6 months of surgical treatment) and late death (more than 6 months after surgical treatment) compared to surviving until the end of follow-up by multivariable multinomial logistic regression analysis.

Factors	Death within 6 months	p value	Death after 6 months	p value
Factors	Adjusted OR (95% CI)^a	p value	Adjusted OR (95% CI)^a	p value
ASA class
1–2	1		1
3	2.63 (0.46–15.14)	0.280	2.94 (1.24–7.00)	0.015
4	7.18 (0.88–58.44)	0.065	3.60 (1.03–12.61)	0.045
CCI score
0	1		1
1–2	0.59 (0.15–2.29)	0.446	1.02 (0.49–2.12)	0.964
⩾3	3.88 (0.61–24.84)	0.153	7.90 (2.20–28.38)	0.002
Alcohol
None	1		1
Misuse	2.02 (0.59–6.93)	0.264	2.83 (1.42–5.67)	0.003
Thrombocyte (× 10⁹ L)
<360	1		1
⩾360	7.01 (1.92–25.54)	0.003	1.00 (0.38–2.59)	0.993
T stage
T1–T2	1		1
T3	16.35 (1.40–191.15)	0.026	1.43 (0.20–10.09)	0.720
T4	3.06 (0.94–9.95)	0.064	1.92 (0.98–3.79)	0.059
N stage
N0	1		1
N1	0.28 (0.02–4.17)	0.358	1.94 (0.73–5.17)	0.186
N2	5.72 (1.30–25.11)	0.021	2.47 (0.99–6.17)	0.054
Tracheostomy
No	1		1
Yes	9.15 (1.53–54.82)	0.015	0.93 (0.40–2.16)	0.864
LOS (days)
<10	10.04 (1.53–65.79)	0.016	2.32 (0.90–6.03)	0.083
10–19	1		1
⩾20	12.04 (2.69–53.87)	0.001	2.33 (0.97 -5.62)	0.060
Complication
None	1		1
Medical	1.33 (0.26–6.67)	0.731	2.95 (1.14–7.63)	0.025
Surgical	0.06 (0.00–0.89)	0.041	1.00 (0.38–2.62)	0.996
Both	0.31 (0.06–1.65)	0.168	0.90 (0.32–2.53)	0.838
Oncological treatment
Follow-up or death before
Oncological treatment	14.49 (2.87–73.19)	0.001	0.74 (0.33–1.67)	0.468
Radiotherapy	1		1
Chemoradiotherapy	0.56 (0.09–3.66)	0.548	0.55 (0.20–1.54)	0.254

ASA: American Society of Anesthesiologists; CCI: Charlson Comorbidity Index; CI: confidence interval; LOS: length of stay; N: lymph node; OR: odds ratio; T: tumor.

Adjusted for other variables included in the model.

Patients with early death

Most of the patients with early death had a CCI score of 0–1. When taking age into account, none of them had an ACCI score of 0 and only two patients had a score of 1. Half (n = 19) of these patients had an ACE-27 score of 3. Only 10 of these 36 patients were found to have NRS2002 scores recorded, and one of these patients was at serious risk of malnutrition.

Immunosuppressive medication was used preoperatively by five patients (13.9%) and anticoagulant medication by seven patients (19.4%). The location of the tumor in patients with early death was most frequently the tongue (33.3%) and mandible (27.8%). Most patients (66.7%) had T4 tumor stage. The lymph node class was N0 in 14 patients (38.9%) and N2 in 19 patients (52.8%). All 317 patients in this study had a metastasis class of M0. All early-death patients, with the exception of one sinonasal undifferentiated carcinoma (SNUC), had squamous cell carcinoma. According to the Statistics Finland, in the group of early death, only nine (25%) had an underlying cause of death other than HNC: six died of cardiovascular disease (myocardial infarction, ischemic heart disease, atherosclerosis, congestive heart failure, and ventricular fibrillation), two of other cancers, and one of meningitis. Nine patients had metastatic HNC confirmed from patients’ charts. Of the nine patients with no complications, six died of HNC.

Anterolateral thigh flap (ALT) was used for most of the 36 patients (n = 25, 69.4%). Tracheostomies (n = 31, 86.1%) and PEGs (n = 28, 77.8%) were required in a large proportion of these patients (Table 4).

Table 4.

Surgical data of 317 patients undergoing free flap reconstruction after surgery for head and neck cancer during 2013–2017.

	Died within 6 months of surgery (n = 36)	Died after 6 months of surgery (n = 77)	Survived (n = 204)
Primary lesion (n)
Tongue	12	24	56
Floor of mouth	6	14	26
Mandible	10	19	42
Maxilla	2	9	30
Buccal mucosa	3	1	21
Tonsilla	1	5	6
Palate	2	1	11
Larynx–hypopharynx	0	3	7
Other	0	1	5
T class (n)
T1	1	17	60
T2	7	16	65
T3	4	4	6
T4	24	40	71
Missing data	0	0	2
N class (n)
N0	14	37	139
N1	3	13	25
N2	19	27	38
Free flap (n)
RFA	3	31	85
ALT	25	31	75
LD	2	1	7
Scapula/parascapula	1	0	1
Fibula	0	2	4
DCIA	2	3	10
TFL	0	1	0
Vastus lateralis muscle flap	0	1	0
TAPAS	1	1	5
Two simultaneous flaps	2	3	6
Ulnaris	0	1	3
Suralis	0	0	5
LAF	0	1	1
Peroneal flap	0	0	1
TRAM	0	1	0
Rectus abdominis free flap	0	0	1
PEG (n)	28	54	97
Tracheostomy (n)	31	46	101

ALT: Anterolateral thigh perforator flap; DCIA: Deep circumflex iliac artery bone flap; LAF: Lateral arm flap; LD: Latissimus dorsi muscle; N: lymph node; PEG: percutaneous endoscopic gastrostomy; RFA: Radial forearm flap; T: tumor; TAPAS: temporal artery posterior auricular skin flap; TFL: Tensor fascia lata flap; TRAM: Transverse rectus myocutaneous flap.

However, 5 of these 36 patients (13.9%) received postoperative radiotherapy and 4 (11.1%) postoperative chemoradiotherapy. Radiotherapy was discontinued for three patients. One patient was unable to undergo the recommended chemotherapy due to elevated creatinine levels. Meanwhile, 10 patients were not recommended or were not eligible for postoperative treatment due to underlying medical conditions or due to postoperative treatment being deemed unnecessary. Patients were hospitalized for a median of 21 (range 4–45) days, and the duration of intensive care was a median of 4.5 (range 2–26) days.

Complications in early-death patients

Patient charts were reviewed regarding complications within 30 days of surgery (Table 5). Of the 36 early-death patients, 27 (75%) had a complication and most (n = 22) had several complications. In total, 13 patients (36.1%) had pneumonia. Six patients (16.7%) had to be re-intubated and five of these underwent tracheostomy. Delirium was present in five patients (13.9%). However, 15 patients (41.7%) had an unplanned return to the operating room and 6 patients were re-admitted to intensive care (16.7%). In addition, 25 patients (69.4%) had medical complications, 19 (52.8%) surgical complications, and 15 (41.7%) had both; with only 9 patients having no complications. Complications in each demographic group were graded according to the Clavien–Dindo Classification (data not shown). In early-death patients, 23 (63.9%) had a severe complication (Grade III–V) according to Clavien–Dindo classification. Only seven patients had a Grade V complication, and they were all aged 60 years or older, ASA class 3–4, and had ACE-27 score 2–3. However, 19 (52.8%) of the early-death patients had ACE-27 score 3. There was a significant difference in the number of complications between early-death patients versus those patients surviving more than 6 months (p < 0.001).

Table 5.

Summary of medical and surgical complications incurred by 36 patients’ death within 6 months of free flap reconstruction for head and neck malignancy.

	No. of complications (n)
Medical
Respiratory failure (and re-intubation)	21
Pneumonia/bronchitis	13
Delirium	5
NSTEMI/STEMI	4
Pulmonary edema/heart failure	4
Atrial fibrillation	3
Other infection (urinary tract, meningitis)	3
Sepsis	2
Stroke	1
CIP/CIM	1
ARDS	1
Hemodynamic instability	1
Vomiting, ileus	1
Total	60
Surgical
Surgical site hematoma	5
Surgical site infection	5
Partial flap failure (OR revision)	5
Tracheostomy
Edema	3
Mucous	1
Exhaustion	1
Pleural puncture	3
Wound revision/dehiscence	2
Fistula	2
Nerve damage	2
Edema (poor lymphatic circulation/dysphagia (PEG insertion))	2
Chylous leak	1
Peritonitis due to PEG dislodgement	1
Total flap failure	1
Abscess	1
Total	35

ARDS: acute respiratory distress syndrome; CIP: critical illness polyneuropathy; CIM: critical illness myopathy; NSTEMI: non-ST elevation myocardial infarction; OR: operating room; PEG: percutaneous endoscopic gastrostomy; STEMI: ST elevation myocardial infarction.

Complications in late-death and surviving patients

Of the 77 late-death (death more than 6 months after surgery) patients, 54 patients (70.1%) had two or more complications. In addition, 101 patients (49.5%) surviving until the end of the follow-up period had two or more complications. Of the late-death and surviving patients, altogether 91 (32.4%) patients had a severe complication. ACE-27 score 3 was found for 17 late-death patients (22.1%) and 17 surviving patients (8.3%). There was a significant difference in the number of complications between late-death patients versus those patients surviving through the follow-up period (p = 0.002).

Discussion

We performed a registry-based study on early mortality, that is, death within 6 months of microvascular free tissue reconstruction of HNC ablative surgery with curative intent. In total, 317 patients with curative intent of treatment and with no prior HNC treatment were included. There were 36 early deaths (11.4%) in this series. Age of 75 years and older, increased ACE-27 score, elevated thrombocytes, and advanced tumor stage were independent risk factors for early mortality after operation according to multivariable binary logistic regression. Patients with early death had a considerable number of complications and most died of the primary malignant disease. This study identified that clinical characteristics for the risk of early death after free flap reconstruction differ only slightly from those reported for the general HNC population.¹⁵ Similar risk factors for early death were found in a Danish study reporting on 11,419 HNC patients treated with curative intent RT/CRT between 2000 and 2017.²⁴

Only few studies have documented early mortality, defined as 30-day mortality or hospital death, after HNC free flap reconstruction. Male sex, low BMI, low preoperative albumin, and higher postoperative CRP are the factors that affect survival within 6 months of surgery.²² This study had comparable findings regarding low BMI and low preoperative albumin in univariable logistic regression analysis but were no longer significant in multivariable logistic regression analysis (Supplemental Table 1). Stage IV was significantly associated with postoperative in-hospital mortality in a series of 804 HNC patients with free flap reconstruction.¹⁷ In this study, tumor class T3 and lymph node class N2 were associated with early death. High platelet counts have been associated with poor survival in patients with head and neck squamous cell carcinoma,²⁵ which was confirmed in this study. This is not surprising due to the known functions and interactions of platelets, for example, the forming of blood clots, modulation of the immune response, and possibly the facilitation of cancer progression.²⁵ In line with previous studies, in the group of early death, patients with a tracheostomy and those with a hospital stay of more than 20 days had significantly more complications than late-death and surviving patients.^22,26

The focus of this study was to assess predictors for early death after major head and neck surgery with free flap reconstruction. According to multinomial logistic regression analysis, comparing death within 6 months and after, in the group of death after 6 months ASA class 3–4, CCI of 3 or more, alcohol misuse, and medical complications were significant risk factors. However, risk of early death was affected by age above 75 years, an increased ACE-27 score, high T and N classification, and elevated thrombocytes. These slightly differing factors deserve attention in treatment decision-making and in the planning of follow-up monitoring of this patient population.

Patient comorbidities have an obvious high impact on complications and mortality.^6,9,10 Complications occurred in 75% of early-death patients in this study, which is comparable to the complication rate of a recent study, reporting on free flap patients who had one or more complications (72%).⁹ While complication rates vary widely (20%–72%) between studies, microvascular surgery is, nevertheless, considered to be safe,^4,7 with a 30-day postoperative mortality rate of 2.7%,¹¹ which is in line with our data 2.2% (n = 7). In this study, the complication rate decreased as the ACE-27 comorbidity score decreased between the patient groups (early-death versus late-death versus surviving patients). We analyzed the overall mortality of HNC patients and the risk factors affecting it. Majority of HNC patients die from the primary disease and thus, the risk factors for disease-specific survival are expected to be very similar.

Age at diagnosis, TNM classification, and comorbidities impact short-term mortality of the patient with a newly diagnosed HNC.²⁷ When planning treatment at a multidisciplinary meeting, one should pay particular attention to age, TNM classification, and ACE-27 score. In addition, preoperative inflammatory markers, low albumin, and low BMI of 19.9 or less should be considered. As part of enhanced recovery, it is important to take into account ambulation, prevention of infection, closure of tracheostomy, and keeping the length of stay in the ICU as short as possible.²⁸ However, patients must be informed comprehensively on treatment options and their wishes are of utmost importance. In addition, prehabilitation of patients is beneficial for their recovery. Before conclusions can be drawn about the factors that influence early death after HNC operation, larger studies are needed. In the future, the pooled research results and available algorithms could aid in predicting serious postoperative complications and possible early postoperative deaths more reliably.

The limitations of this study include that it is a retrospective and single-center study with a relatively limited number of patients. For example, the confidence interval for the T3 class analysis was wide and, thus, not as reliable. Nonetheless, the series size exceeds many previous reports, and the long follow-up time remains a strength of the study. However, the management of HNC in Finland (population of 5.5 million) is centralized to the five university hospitals. The catchment area of HUS includes more than 2 million residents, or 39% of the entire Finnish population. Therefore, the present series represents a consecutive 5-year patient cohort of a large academic tertiary care hospital. The optimal treatment strategy and follow-up schedule for each patient are planned at a weekly multidisciplinary tumor board. Currently, more than 100 head and neck free tissue transfers are performed at HUS annually.²⁹ The active microvascular reconstructive approach in the surgical treatment of oral tongue cancer at HUS has recently been reported.³⁰

Recorded data regarding clinical disease coding and comorbidities in hospital registries have been stated to be deficient in earlier studies.^31,32 However, the data in this study were manually validated completely from electronic patient charts. Unfortunately, information on the duration of care for patients, who were referred to a convalescent care facility after discharge from the university hospital, was unavailable. Consequently, the actual length of care in total of some patients was not known.

In conclusion, HNC patients aged 75 years and older, with an increased ACE-27 score, high T and N classification, or elevated thrombocytes were identified as having an increased risk of early postoperative mortality after microvascular free flap operation. Therefore, preoperative assessment should pay particular attention to these factors. To guide preoperative decision-making in patients having major head and neck surgery with free flap reconstruction, clinicians need to be aware of all the relevant factors that determine treatment outcome.

Supplemental Material

sj-xlsx-1-sjs-10.1177_14574969221117010 – Supplemental material for Risk factors for evaluating early mortality after microvascular reconstruction of head and neck cancers

Supplemental material, sj-xlsx-1-sjs-10.1177_14574969221117010 for Risk factors for evaluating early mortality after microvascular reconstruction of head and neck cancers by Teija Nieminen, Morag Tolvi, Patrik Lassus, Tommy Wilkman, Lasse Lehtonen and Antti Mäkitie in Scandinavian Journal of Surgery

Supplemental Material

sj-xlsx-2-sjs-10.1177_14574969221117010 – Supplemental material for Risk factors for evaluating early mortality after microvascular reconstruction of head and neck cancers

Supplemental material, sj-xlsx-2-sjs-10.1177_14574969221117010 for Risk factors for evaluating early mortality after microvascular reconstruction of head and neck cancers by Teija Nieminen, Morag Tolvi, Patrik Lassus, Tommy Wilkman, Lasse Lehtonen and Antti Mäkitie in Scandinavian Journal of Surgery

Footnotes

Acknowledgements

The authors thank statistician Tero Vahlberg for his statistical work.

Author contributions

A.M., L.L., T.N., and M.T. contributed in study design; T.N. participated in data collection; all authors contributed in data interpretation; T.N., M.T., and A.M participated in writing the article. All authors have critically reviewed and accepted the submitted version of the article.

Declaration of conflicting interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The work was supported by the Helsinki University Hospital Research Fund.

ORCID iDs

Teija Nieminen

Morag Tolvi

Tommy Wilkman

Supplemental material

Supplemental material for this article is available online.

References

Bray

Ferlay

Soerjomatarm

, et al: Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68(6):394–424.

Machiels

René Leemans

Golusinski

, et al: Squamous cell carcinoma of the oral cavity, larynx, oropharynx and hypopharynx: EHNS-ESMO-ESTRO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol 2020;31(11):1462–1475.

Rogers

Brown

Wooglar

, et al: Survival following primary surgery for oral cancer. Oral Oncol 2009;45(3):201–211.

Pohlenz

Klatt

Schön

, et al: Microvascular free flaps in head and neck surgery: Complications and outcome of 1000 flaps. Int J Oral Maxillofac Surg 2012;41(6):739–743.

Nouraei

Middleton

Hudovsky

, et al: Role of reconstructive surgery in the management of head and neck cancer: A national outcomes analysis of 11,841 reconstructions. J Plast Reconstr Aesthet Surg 2015;68(4):469–478.

McMahon

MacIver

Smith

, et al: Postoperative complications after major head and neck surgery with free flap repair—Prevalence, patterns, and determinants: A prospective cohort study. Br J Oral Maxillofac Surg 2013;51(8):689–695.

Schwam

Sosa

Roman

, et al: Complications and mortality following surgery for oral cavity cancer: Analysis of 408 cases. Laryngoscope 2015;125(8):1869–1873.

Cannady

Hatten

Bur

, et al: Use of free tissue transfer in head and neck cancer surgery and risk of overall and serious complication(s): An American College of Surgeons-National Surgical Quality Improvement Project analysis of free tissue transfer to the head and neck. Head Neck 2017;39(4):702–707.

McMahon

Handley

TPB

Bobinskas

, et al: Postoperative complications after head and neck operations that require free tissue transfer—Prevalent, morbid, and costly. Br J Oral Maxillofac Surg 2017;55(8):809–814.

10.

Eskander

Kang

Tweel

, et al: Predictors of complications in patients receiving head and neck free flap reconstructive procedures. Otolaryngol Head Neck Surg 2018;158(5):839–847.

11.

Ch’ng

Choi

Elliott

, et al: Relationship between postoperative complications and survival after free flap reconstruction for oral cavity squamous cell carcinoma. Head Neck 2014;36(1):55–59.

12.

Talmor

Kelly

: How to better identify patients at high risk of postoperative complications? Curr Opin Crit Care 2017;23(5):417–423.

13.

Vosler

Orsini

Enepekides

, et al: Predicting complications of major head and neck oncological surgery: An evaluation of the ACS NSQIP surgical risk calculator. J Otolaryngol Head Neck Surg 2018;47(1):21.

14.

Farnebo

Malila

Mäkitie

, et al: Early death among head and neck cancer patients. Curr Opin Otolaryngol Head Neck Surg 2016;24(2):115–120.

15.

Talani

Mäkitie

Beran

, et al: Early mortality after diagnosis of cancer of the head and neck—A population-based nationwide study. PLoS ONE 2019;14(10):e0223154.

16.

Tanaka

Sakuraba

Miyamoto

, et al: Analysis of operative mortality and post-operative lethal complications after head and neck reconstruction with free tissue transfer. Jpn J Clin Oncol 2011;41(6):758–763.

17.

Pohlenz

Klatt

Schmelzle

, et al: The importance of in-hospital mortality for patients requiring free tissue transfer for head and neck oncology. Br J Oral Maxillofac Surg 2013;51(6):508–513.

18.

Nouraei

Middleton

Hudovsky

, et al: A national analysis of outcome of major head and neck cancer surgery: Implications for surgeon-level data publication. Clin Otolaryngol 2013;38(6):502–511.

19.

Joo

Cho

Park

, et al: Surgical morbidity and mortality in patients after microvascular reconstruction for head and neck cancer. Clin Otolaryngol 2018;43(2):502–508.

20.

Chicco

Huang

Cheng

: Mortality within 30 days after head and neck free flap reconstruction: A systematic review. J Craniofac Surgery 2021;32(5):1738–1741.

21.

L’Esperance

Kallogjeri

Yousaf

, et al: Prediction of mortality and morbidity in head and neck cancer patients 80 years of age and older undergoing surgery. Laryngoscope 2018;128(4):871–877.

22.

Lahtinen

Koivunen

Ala-Kokko

, et al: Short- and long-term mortality and causes of death after reconstruction of cancers of the head and neck with free flaps. Br J Oral Maxillofac Surg 2019;57(1):21–28.

23.

Dindo

Demartines

Clavien

: Classification of surgical complications: A new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg 2004;240(2):205–213.

24.

Jensen

Vogelius

Kristensen

, et al: Early mortality after radical radiotherapy in head and neck cancer—A nationwide analysis from the Danish Head and Neck Cancer Group (DAHANCA) database. Clin Oncol 2021;33(1):57–63.

25.

Takenaka

Oya

Kitamiura

, et al: Platelet count and platelet-lymphocyte ratio as prognostic markers for head and neck squamous cell carcinoma: Meta-analysis. Head Neck 2018;40(12):2714–2723.

26.

Poisson

Longis

Schlund

, et al: Postoperative morbidity of free flap in head and neck cancer reconstruction. Clin Oral Investig 2019;23(5):2165–2171.

27.

Datema

Ferrier

van der Schroeff

, et al: Impact of comorbidity on short-term mortality and overall survival of head and neck cancer patients. Head Neck 2010;32(6):728–736.

28.

HØjvig

Pedersen

Charabi

, et al: Microvascular reconstruction in head and neck cancer—Basis for the development of an enhanced recovery protocol. JPRAS Open 2020;26:91–100.

29.

Husso

Mäkitie

Vuola

, et al: Evolution of head and neck microvascular reconstructive strategy at an academic centre: An 18-year review. J Reconstr Microsurg 2016;32(4):294–300.

30.

Mäkitie

Kamali

Mroueh

, et al: A descriptive study highlighting the differences in the treatment protocol for oral tongue cancer in Sweden and Finland. Acta Otolaryngol 2020;140(2):188–194.

31.

Bottle

Aylin

: Comorbidity scores for administrative data benefited from adaptation to local coding and diagnostic practices. J Clin Epidemiol 2011;64(12):1426–1433.

32.

Naran

Hudovsky

Antscherl

, et al: Audit of accuracy of clinical coding in oral surgery. Br J Oral Maxillofac Surg 2014;52(8):735–739.

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